酰肼类席夫碱过渡金属配合物的合成、结构表征和生物活性的研究
|
摘要
酰肼类席夫碱是一类非常重要的含氮配体，由于其生物多样性，对它们配合物的研究已成为生物无机化学的热点。我们合成了上百种酰肼类席夫碱及其配合物，有60多种化合物通过单晶X-射线结构分析确定了分子和晶体结构。本论文选择65种有代表性的席夫碱及其配合物，其中26种席夫碱配合物是新的。通过元素分析、~1H-NMR和质谱方法确定了24种酰肼类化合物(3a-4d、4h-4o)的结构，通过元素分析和单晶X-射线结构分析确定了5种酰肼类席夫碱配(4c-4g)和18种配合物(5a-6a、6c、6f、7a、7c、8a-8f、9a-9d)的晶体和分子结构，其余8种配合物6b、6d、6g-6j、7b)的结构是通过元素分析和红外光谱等方法确定的。
异烟酰肼是一种抗结核临床药物，具有很好的细胞毒活性，酰肼类化合物具有与异烟酰肼相似的结构，都含有酰基和肼基。同时此类化合物又有很强的螯合能力，能与各种金属配位，形成各种的配合物。基于上述知识，我们对上述化合物的人体海拉细胞毒活性进行了测量，结果正如我们所料，所有酰肼类化合物都有细胞毒活性，有的化合物(如4b)的细胞毒活性与临床药物—5-氟尿嘧啶(5-氟尿嘧啶是一种临床抗肿瘤药物)接近。令人振奋的是：配合物往往比配体具有更好的细胞毒活性，这可能是由于配体轨道和金属离子轨道的交叠作用，导致金属离子的极化率在很大范围内减小。同时增加了整个螯合环中π电子的离域化作用，增强了配合物的亲脂性。亲脂性的增加使配合物易于渗透细胞，当配合物进入细胞内，与病毒的微量金属生成药物-金属-酶的混合配合物而阻止病毒的复制。同时，病毒的核酸和蛋白又是很好的配位体，与从配合物中解离出来的金属离子作用，使一些活性官能团失活，因而具有明显的抗病毒活性。在铜、钴、镍、锰、锌五种过渡金属配合物中，铜配合物的生物活性往往表现得最好，锌、锰次之，钴一般，镍最差，具体的原因还需进一步探讨。除合成了酰肼类席夫碱过渡金属配合物外，我们还合成了一系列不含酰肼类过渡金属配合物与它们进行比较，从结构上分析了酰肼类席夫碱过渡金属配合物细胞毒活性较好的原因。除此以外，我们还合成了一些结构新颖的查尔酮二聚物和类似物，对它们的合成机理进行了探讨，测量了它们七种抗菌活性和KB细胞的细胞毒活性，并对结构和活性之间的关系做了讨论。
Schiff bases with hydrazide are a kind of very important ligand containing N atoms which are easy prepared by simple self-condensation of aldehydes or ketones with hydrazide. Many ligands generally have been designed to contain additiona donor groups (0, S, P, etc.) and it makes them good candidates for agents and metal ion complexation. A number of Schiff bases with hydrazide have been claimed to possess good antibacterial, anticancer, antifungal, anticonvulsant, antinflammatory, antimalarial and antituberculosis activities. However, relationship between the structures and biological activities is dimness up to date.
In order to investigate relationships between the structures and biological activities, this dissertation investigates the synthesis, characterization and biological activities of 65 Schiff base with hydrazide and their transition metal complexes as potential agents for therapeutic purpose. 24 Schiff base with hydrazide (3a-4d, 4h-4o) were prepared by the reaction of aldehyde with hydrazide and their structures were determined by element analysis, ~1H-NMR and MS. 5 Schiff bases with hydrazide(4c-4g) were characterized by X-ray diffraction. A series of Schiff base ligands were reacted with transitional metal salt (i.e., Ni(OAc)_2·4H_2O, Zn(Ac)_2·4H_2O) to yield a series of transition metal complexes. In most cases, reaction with two equival of ligand in mixture of ethanol and pyridinium yielded mononuclear, dinuclear or trinuclear complexes and formed octahedral or pyramid coordination polyhedron. In this article, 26 complexes (5a-9d) were first sythesised and their elemental analyses, crystal structure, IR spectra and biological activities have been investigated. It should be emphasized that crystal structures of eighteen Schiff base compounds were obtained for the first time. From the analytiacl data, it has been concluded that all the compounds of the hydrazide derivatives showed potent cytotoxic activities and its complex is more ative than the ligand. To the best of our knoeledge, the increased lipophilicity may be responsible for this increased cytotoxic activity. The cytotoxic activity of copper complex is most active among five transion metal complexes. Little is understood up to date about the reason and many efforts need to do. At the same time, some novel chalcone analogys have been sythesised and their reation mechanism and biological activities have been proposed. In a word, chalcone derivations possess weak antimicrobial activity. Thus, it is not suitable for the nitrochalcones to be antimicrobial agents.
异烟酰肼是一种抗结核临床药物，具有很好的细胞毒活性，酰肼类化合物具有与异烟酰肼相似的结构，都含有酰基和肼基。同时此类化合物又有很强的螯合能力，能与各种金属配位，形成各种的配合物。基于上述知识，我们对上述化合物的人体海拉细胞毒活性进行了测量，结果正如我们所料，所有酰肼类化合物都有细胞毒活性，有的化合物(如4b)的细胞毒活性与临床药物—5-氟尿嘧啶(5-氟尿嘧啶是一种临床抗肿瘤药物)接近。令人振奋的是：配合物往往比配体具有更好的细胞毒活性，这可能是由于配体轨道和金属离子轨道的交叠作用，导致金属离子的极化率在很大范围内减小。同时增加了整个螯合环中π电子的离域化作用，增强了配合物的亲脂性。亲脂性的增加使配合物易于渗透细胞，当配合物进入细胞内，与病毒的微量金属生成药物-金属-酶的混合配合物而阻止病毒的复制。同时，病毒的核酸和蛋白又是很好的配位体，与从配合物中解离出来的金属离子作用，使一些活性官能团失活，因而具有明显的抗病毒活性。在铜、钴、镍、锰、锌五种过渡金属配合物中，铜配合物的生物活性往往表现得最好，锌、锰次之，钴一般，镍最差，具体的原因还需进一步探讨。除合成了酰肼类席夫碱过渡金属配合物外，我们还合成了一系列不含酰肼类过渡金属配合物与它们进行比较，从结构上分析了酰肼类席夫碱过渡金属配合物细胞毒活性较好的原因。除此以外，我们还合成了一些结构新颖的查尔酮二聚物和类似物，对它们的合成机理进行了探讨，测量了它们七种抗菌活性和KB细胞的细胞毒活性，并对结构和活性之间的关系做了讨论。
Schiff bases with hydrazide are a kind of very important ligand containing N atoms which are easy prepared by simple self-condensation of aldehydes or ketones with hydrazide. Many ligands generally have been designed to contain additiona donor groups (0, S, P, etc.) and it makes them good candidates for agents and metal ion complexation. A number of Schiff bases with hydrazide have been claimed to possess good antibacterial, anticancer, antifungal, anticonvulsant, antinflammatory, antimalarial and antituberculosis activities. However, relationship between the structures and biological activities is dimness up to date.
In order to investigate relationships between the structures and biological activities, this dissertation investigates the synthesis, characterization and biological activities of 65 Schiff base with hydrazide and their transition metal complexes as potential agents for therapeutic purpose. 24 Schiff base with hydrazide (3a-4d, 4h-4o) were prepared by the reaction of aldehyde with hydrazide and their structures were determined by element analysis, ~1H-NMR and MS. 5 Schiff bases with hydrazide(4c-4g) were characterized by X-ray diffraction. A series of Schiff base ligands were reacted with transitional metal salt (i.e., Ni(OAc)_2·4H_2O, Zn(Ac)_2·4H_2O) to yield a series of transition metal complexes. In most cases, reaction with two equival of ligand in mixture of ethanol and pyridinium yielded mononuclear, dinuclear or trinuclear complexes and formed octahedral or pyramid coordination polyhedron. In this article, 26 complexes (5a-9d) were first sythesised and their elemental analyses, crystal structure, IR spectra and biological activities have been investigated. It should be emphasized that crystal structures of eighteen Schiff base compounds were obtained for the first time. From the analytiacl data, it has been concluded that all the compounds of the hydrazide derivatives showed potent cytotoxic activities and its complex is more ative than the ligand. To the best of our knoeledge, the increased lipophilicity may be responsible for this increased cytotoxic activity. The cytotoxic activity of copper complex is most active among five transion metal complexes. Little is understood up to date about the reason and many efforts need to do. At the same time, some novel chalcone analogys have been sythesised and their reation mechanism and biological activities have been proposed. In a word, chalcone derivations possess weak antimicrobial activity. Thus, it is not suitable for the nitrochalcones to be antimicrobial agents.
引文
[1] H. Schiff, Annis Chem, 1864, 131, 118.
[2] S. Handa, V. Gnanadesikan, S.Matsunaga, M.Shibasaki, J. Am. Chem. Soc., 2007, 129, 4900-4901.
[3] C. Chen, L. Hong, Z.-Q.Xu, L.Liu, R.Wang, Org. Lett., 2006, 8, 2277-2280.
[4] G. Occhipinti, V. R. Jensen, H. R. Bjorsvik, J. Org. Chem., 2007, 72, 3561-3564.
[5] X.-P.Yang, Jones R. A., M. M.Oye, A. L Holmes, W.-K.Wong, Cryst. Growth Des., 2006, 6, 2122-2125.
[6] J. A. Riddle, S. P. Lathrop, J. C. Bollinger, D. Lee, J. Am. Chem. Soc. 2006; 128(34); 10986-10987.
[7] R. Jarvo Elizabeth, M. L. Brian, N. J. Eric., Angew. Chem. Int. Edi., 2005, 44, 6043-6046.
[8] M. Kazuhiro, Y.Sawada, S. Bunnai, S.Ken, K.Tsutomu, Angew. Chem. Int. Edi., 2005, 44, 4935-4939.
[9] O. Akihiro, S. Tomoyuki, T.Ohshima, H.Masu, Y.Kentaro, S.Masakatsu, Angew. Chem. 2005, 117, 4640-4643.
[10] J. L. Sessler, E. Tomat, V. M. Lynch, J. Am. Chem. Soc. 2006; 128(34); 10986-10987.
[11] T. Tanaka, Y. Yasuda, M. Hayashi, J. Org. Chem., 2006, 71, 7091-7093.
[12] 游效曾，孟庆金，韩万书主编 配位化学进展．-北京：高等教育出版社，2000．
[13] M. Eddaoudi, D. B Moler., H.L.Chen, T.M.Reineke, M. Okeeffe, O.M.Yaghi, Acc. Chem. Res., 2001, 34, 319.
[14] S.-S. Chui., S.M.F.Lo, J.P.H.Charmant, A.G.Orpen, I.D.Williams, Sci., 1999, 283, 1148.
[15] 林君，庞茂林，韩银花，于敏，张洪杰，无机化学学报，2001，17，153．
[16] Q. -G. Meng, H.-J.Zhang, S.-B.Wang, L.-S.Fu, Y.-X.Yang, Mater. Lett., 2000, 45,213.
[17] 林君，苏锵，稀土，1994，15，42．
[18] T. Jin, S.Tsutsumi, Y. Deguchi, K. Machid, J. Electrochem. Soc., 1995, 142, L195.
[19]. G.. Qian, M.-J. Wang, J. Phys. Chem. Solid, 1997, 58, 375.
[20] 王金龙，武汉大学硕士学位论文，2003．
[21] 袁良杰，武汉大学博士学位论文，2003．
[22] K. Dey, J. Scient. Ind. Res. India, 1974, 33, 76.
[23] F. P. Dwyer, D. P. Mellor, Chelating Agents and Metal Chelates. New York: Academic Press Inc, 1964.
[24] J. W. Smith. In: Patai S. The Chemstry of Carbon-Nitrogen Double Bond. London: Interscience Publisher Ltd, 1970, Chapter 5.
[25] H. Malcolm, C. C. Judith, Gallucci, and H.-S. Zhen, Inorg. Chem., 2001, 40, 5051.
[26] A. K. Patra, M. M. Olmstead and P. K. Mascharak, Inorg. Chem., 2002, 41, 5403;
[27] C. Olivier, C. Francoise, D. Andrea, S. Claudio, V. S. Joris, and G. F. V. Maria, Inorg. Chem., 2003, 42, 6432.
[28] J. P. Cean, F. L Jean., L. Christine, G. L. Pascal, and D. Francoise and N. Keitaro, Inorg. Chem. 2005, 44, 1973.
[29] D. Renata, A. Bart, L. Nele, D. Ileana, D. Valerian, V. Francis, J Coord. Chem. Rev., 2005, 249, 3055.
[30] M. R. Jose., R. Horacio, C. Armando, and S. P. G. L Rosa., and L. K. N. Christine, F. Norberto, Chem. Mater., 2006, 18, 1174.
[31] K. Sah Ajay, T. Tomoaki, and M. Masahiro, Inorg. Chem., 2006, 45, 2083.
[32] M. B. Virginie, Saeed I. K., and Mahdi M. A., Inorg. Chem., 2001, 40, 6767.
[33] P. Reinhard, L. Stefan, T. Carsten, A. O.Michael and S. Ekkehard, Inorg. Chem., 2003, 42, 8231.
[34] G. Park, F. Lu H., N. Ye, M. W. Brechbiel, S. V. Torti, F. M. Torti, and R. P. Planalp, JBIC 1998, 3,449.
[35] V. Paola, I. Matteo, A. D. Irini, L. C. Paolo, B. Bernadetta, L. Roberta, Eur. J. Med. Chem., 2006, 41, 624.
[36] F.-Y. Chen, W.-K. Cao, S.-Y. He, B.-H. Wang, Y.-M. Zhang, Acta Phys. -China. Sin., 2006, 22(3), 280-285.
[37] D. L. Alessandro, O. Valentina, S. Barbara, C. Cenzo, L. S. Maria and T. C. Maria, J. Antimicrob. Chemoth., 2002, 49, 275.
[38] T. C. Maria, C. Cenzo, O. Valentina, C. P. Maria, Maria L. Schivo, D. L. Alessandro, Eur. J. Med. Chem., 1999, 34, 1071.
[39] M. Patricia, L. Virginie, S. Christian, and G. Philippe, Bioorg. Med. Chem. Let., 2006, 16, 31.
[40] T. B. Chaston, D. R. Richardson, J Biol Inorg Chem, 2003, 8, 427.
[41] B. B. Safoklov, E. G. Atovmyan, L. A. Nikonova, V. V. Tkachev, and S. M. Aldoshin, Russ. Chem. B., 2002, 51, 2224.
[42] R. Maccari, R. Ottanaa and M. G. Vigorita, Bioorg. Med. Chem. Let., 2005, 15, 2509.
[43] D. Sriram, P. Yogeeswari and K. Madhu, Bioorg. Med. Chem. Let., 2005, 15, 4502.
[44] D. Sriram, P. Yogeeswari and K. Madhu, Bioorg. Med. Chem. Let., 2006, 16, 876.
[45] P. S. J. Floriano, E .Javier, L. F. Marcelled., P. M. Yvonne, V. N. d. S. Marcus, R. A. V. Thatyana, L. W. James, M. S. V. W. Solange, J. Mol. Struct., 2006, 788, 63.
[46] D. G. Rando, A. C. Doriguetto, J. Ellena, S. D. N. Leite, E. A. Varanda, E. I. Ferreira, Eur. J. Med. Chem., 2006, 41, 1196.
[47] D. D. Yu and B. M. Forman, Bioorg. & Med. Chem. Let., 2005, 15, 1311.
[48] S. Sivaramaiah and R. P. Raveendra, J. Anal. Chem., 2005, 60, 828.
[49] S. Guniz Kuc, ukuCguzel, A. Mazi, F. Sahin, S. Ozturk, J. Stables, Eur. J. Med. Chem., 2003, 38, 1005.
[50] B. -D. Wang, Z. -Y. Yang and T.-R. Li, Bioorg. Med. Chem. Let. 2006, 14, 6012.
[51] C. Xu, H. Y. Mao, H. Y. Zhang, H. L. Liu, J. Mol. Struct., 2003, 658, 59.
[52] W. Xiao, Z. I. Lu, X. J. Wang, C. Y. Su, K. B. Yu, H. Q. Liu, B. S. Kang, Polyhedron, 2000, 19, 1295.
[53] C. Pelizzi, G. Pelizzi, and P. Tatasconi, J. Chem. Soc. Dalton Trans., 1985, 215
[54] C. Lorenzini, C. Pelizzi, G. Pelizzi, and G. Pelizzi, J. Chem. Soc. Dalton Trans., 1983, 721.
[55] Z. H. Liu, C. Y. Duan, J. Hu and X. Z. You, Inorg. Chem., 1999, 38, 1719
[56] 陈小华刘世雄，无机化学学报，2005，21，15．
[57] 胡宗球，吴宇，加兵，施少敏，祝心德，宋发辉，无机化学学报，2005，21，1715．
[58] 孙纲春，曲建强，王流芳，陈耐生，李燕，陈晓光，谢晶曦，无机化学学报，2005，21，1069．
[59] 杨健国，潘富友，李钧敏，无机化学学报，2005，21，1593．
[60] 肖子敬，刘世雄，林墀昌，无机化学学报，2004，20，513．
[61] F. Y. Chen. W. K Cao, S. Y. He, B. H. Wang, Y. M. Zhang, Acta Phys. -Chim. Sin., 2006, 22, 280.
[62] N. R. Sumita, D. D. Mishra, R. C.Maurya and R. N. Nageswara., Polyhedron, 1997, 16, 1825.
[63] S.-Y. He, R. Yang, W.-T. Wu, Q.-Z. Shi, D.-Q. Wang and D.-R. An, Chin. J. Chem., 2005, 23, 1198.
[64] T. Shi, S.Y. He, X. F. Wang, Y.B. Wang, Z.X. Tang and Z.Y. Wen, J. Mol. Struet., 2005, 732, 201.
[65] S. Naskar, S. Biswas, D. Mishra, B. Adhikary, L.R. Falvello, T. Soler, C.H. Schwalbe and S.K. Chattopadhyay, Inorg. Chim.Acta, 2004, 357,4257.
[66] N. K. Singh, Nagendra Singh, G. C. Prasad, h A. Sodhi and Anju Shrivastava, Bioorg. Med. Chrm., 1997, 5,245.
[67] R. M. R. Ottana, B. Bottari, E. Rotondo and M. G. Vigorita, Bioorg. Med. Chem. Let., 2004,14,5731.
[68] B. Bottari, R. Maccari, F. Monforte, R. OttanaA, E. Rotondo and M. G. Vigoritaa, Bioorg. Med. Chem. Let., 2001,11,301.
[69] P. K. Singh, D. N. Kumar, Spectrochimica Acta Part A, 2006,64, 853.
[70] B. Bottari, R. Maccari, F. Monforte, R. OttanaA, E. Rotondo and M. G. Vigorita, Bioorg. Med. Chem. Let., 2000,10,657.
[71] D. R. Richardson and Paul V. Bernhardt, JBIC, 1999,4,266.
[72] F. Cariati, U. Caruso, R. Centore, W. Marcolli, A. De Maria, Panunzi, A. Roviello, and A.Tuzi, Inorg, Chem, 2002,41,6597.
[73] D.B. Wang, B.H.Chen, Y.X. Ma, Syn. React. Inorg. Met-Org. Chem.,1997,27,479.
[74] M. Mohan, M. P. Gupta and L. Chandra, J Chem. Acta, 1988,151,61.
[75] Z. H..Chohan, A.Rauf, Syn. React. Inorg. Met-Org. Chem, 1996,26,591.
[76] M.Kondo, K.Nabari, T. Horiba,, Y. Me,, M. K. Kabir, R. P. Sarker, E. Shimizu, Y. Shimizu,.F.W. Yang, Inorg. Chem. Commun, 2003,6,154.
[77] F. Averseng, P. G. Lacroix, I. Malfant, N. Perisse, and C. L.K. Nakatani, Inorg. Chem, 2001,40,3797.
[78] Z.-L. Lu, M. Yuan, F. Pan, S. Gao, D.-Q. Zhang, and D.-B. Zhu, Inorg. Chem, 2006,45, 3538.
[79] C. A. Bear, J. M. Waters, T. N. Waters, J. Chem. Soc, Dalton Trans, 1974,1059.
[80] (a) Reddy et al. Inorg. Chem, 1998,37,5978; (b) Li et al. Inorg. Chem. Acta, 1998, 271,99.
[81] (a) Christian D. Be'rube', Sandro Gambarotta, and Glenn P. A. Yap, Organometallics, 2003,22,434. (b) T.-F. Jiao and M.-H. Liu, J. Phys. Chem. B, 2005,109,2532. (c) D. Agustin, G. Rima, H. Gornitzka, and J. Barrau, Organometallics, 2000,19,4276. (d)D. Agustin, G. Rima, H. Gornitzka and J. Barrau, Inorg. Chem, 2000, 39, 5492.(e) T.-W. Wong, T.-C. Lau and W.-T. Wong, Inorg. Chem, 1999,38,6181. (f) J. M. McInnes, D. Swallow, A. J. Blake, and P. Mountford, Inorg. Chem, 1998,37,5970. (g) J. M. Rivera, H. Reyes, A. Cortes, and R. Santillan, Chem. Mater, 2006,18,1174.(h) F. Averseng, C. Lepetit, P.I G. Lacroix, and J. P. Tuchagues, Chem. Mater, 2000,12,2225. (g) P. G. Lacroix, S. D. Bella, I. Ledoux, Chem. Mater., 1996, 8, 541. (h) E. Gallo, E. Solari, N. Re, Carlo Floriani, C.-V. Angiola and C. Rizzoli J. Am. Chem. Soc., 1997, 119, 5144.
[82] N. K. Dutt, K.Nag, J. Inorg. Nucl. Chem., 1968, 30, 2493.
[83] R. L. Dutta, B. R. Das, J. Scient. Ind. Res., 1988, 47, 547.
[84] T. Kido, Y. Ikuta, Y. Sunatsuki, Y. Ogawa, N. Re N. Matsumoto, Inorg. Chem., 2003, 42, 398.
[85] Z.-L. You, W.-S. Liu, H.-L. Zhu and H.-K. Fun, Trans.Met.Chem., 2005, 30, 1.
[86] Z.-L. You, H.-L. Zhu, and W.-S. Liu, Trans. Met. Chem., 2004, 29, 653.
[87] Z.-L. You, and H.-L. Zhu, Zinc. Z. Anorg. Allg. Chem., 2004, 630, 2754.
[88] Z.-L. You, H.-L. Zhu, and W.-S. Liu, Z. Anorg. Allg. Chem., 2004, 630, 1617.
[89] Y. Qu, H.-L. Zhu, Z.-L. You and M.-Y. Tan, Molecules, 2004, 9, 949.
[90] F. Averseng, P. G. Lacroix, I. Malfant, N. Perisse, and C. L. K. Nakatani, Inorg. Chem., 2001, 40, 3797.
[91] 黄春辉著．稀土配位化学．北京：科学出版社，1997．
[92] J. Lange, H. Elias, and H. P.J(?)rg Müller and U. Weser, Inorg. Chem., 2000, 39, 3342.
[93] S. G. Telfer, T. Sato, T. Harada, R. Kuroda, J. Lefebvre and D. B. Leznoff, Inorg. Chem., 2004, 43, 6168.
[94] Y.-B. Dong, L. Wang, J.-P. Ma, X.-X. Zhao, D.-Z. Shen and R.-Q. Huang, Crystal Growth & Design, 2006, 0, 1.
[95] Y.-B. Dong, M. D. Smith, H.-C. zur Loye, Inorg. Chem., 2000, 39, 4927.
[96] Y.-B. Dong, M. D. Smith, R. C. Layland, H.-C. zur Loye, Chem. Mater., 2000, 12, 1156.
[97] Y.-B. Dong, X. Zhao, B. Tang, H.-Y. Wang, R.-Q. Huang, M. D. Smith, H.-C. zur Loye, Chem. Commun., 2004, 2, 220.
[98] Y.-B. Dong, P. Wang, R.-Q. Huang, M. D. Smith, Inorg. Chem., 2004, 43, 4727.
[99] Y.-B.Dong, H.-Q. Zhang, J.-P. Ma, R.-Q. Huang, Cryst.Growth Des., 2005, 5, 1857.
[100] K. Ueno, A E. Martell, J. Phys. Chem.,1957, 61,257
[101] (a) N. K. Dutt, Inorg. Chem.,1968, 30, 2779; (b) N. K. Dutt, Inorg. Chem., 1968, 30, 3273.
[102] S. A. Schuetz, C.M. Silvernail, C. D. Incarvito, A. L. Rheingold, J. L. Clark, V. W. Day, and J. A. Belot, Inorg. Chem., 2004, 43, 6203.
[103] Paul D. Benny, Jenny L. Green, Hendrik P. Engelbrecht, Charles L. Barnes and Silvia S. Jurisson, Inorg. Chem., 2005, 44, 2381.
[104] S. A. Schuetz, V. W. Day, R. D. Sommer, A. L. Rheingold and J. A. Belot, Inorg. Chem., 2004, 40, 5292.
[105] 姚克敏，吴大庆，杨卫红，应用化学，1992，9，8．
[106] 杜向东，俞贤达，高等学校化学学报，1997，18，567．
[107] T. S. Reger, K. D. J. Janda, Am. Chem. Soc., 2000, 122, 6929.
[108] G.-J. Kim, S.-H. Kim, Catal. Lett., 1999, 57, 139.
[109] R C. Elder, Aust. J Chem., 1978, 31, 35.
[110] 陈红卫，朱志昂，张智慧等，无机化学学报，1996，12，178．
[111] (a)L. Thunus, R. Lejeune, Coord. Chem. Rev., 1999, 184, 125; (b) K. Wang, R. Li, Y. Cheng, B. Zhu, Coord. Chem. Rev., 1999, 190, 297; (c) J.-C.G. Bünzli, C. Piguet, Chem. Rev., 2002, 102, 1897; (d) H. Tsukube, S. Shinoda, Chem. Rev., 2002, 102, 2389;
[112] W. R. Paryzek, V. Patroniak, J. Lisowski, Coord. Chem. Rev., 1999, 185,451.
[113] V. Comblin, D. Gilsoul, M. Hermann, V. Humblet, V. Jacques, M.Mesbahi, C. Sauvage, J.F. Desreux, Coord. Chem. Rev., 1999, 185,451.
[114] B. Dietrich, P.Viout, J.-M. Lehn, Macrocyclic Chemistry, VCH Verlagsges ellschaft, Weinheim, 1993.
[115] J.-M. Lehn, Supramolecular Chemistry, VCH Verlagsgesellschaft, Weinheim, 1995.
[116] E.C.Constable, Metals and Ligand Reactivity, VCH Verlagsgesellschaft, Weinheim, 1996.
[117] J.R. Fredericks, A.D. Hamilton, in: A.D. Hamilton (Ed.),Supramolecular Control of Structure and Reactivity, Wiley, Chichester, 1996, Chapter 1.
[118] J.W.Steed, J.L.Atwood, Supramolecular Chemistry, Wiley, Chichester, 2000.
[119] J.P. Andre, E. Toth, H. Fischer, A. Seelig, H.R. Maicke, A.E. Merbach,Chem. Eur. J. 1999, 5, 2977.
[120] M. Woods, S. Aime, M. Botta, J.A.K. Howard, J.M. Moloney, M.Navet, D. Parker, M. Port, O. Rousseaux, J. Am. Chem. Soc., 2000,122, 9781.
[121] M. Botta, Eur. J. Inorg. Chem., 2000, 399.
[122] F.A. Dunand, R.S. Dickins, D. Parker, A. Merbach, Chem. Eur. J., 2001, 7, 5160.
[123] S. Aime, D.D.Castelli, F. Fedeli, E. Terreno, J. Am. Chem. Soc., 2002, 124, 9364.
[124] W. Li, G. Parigi, M. Fragai, C.Luchinat, T.J. Meade, Inorg. Chem., 2002, 41, 4018.
[125] M. Woods, Z. Kovacs, S.Zhang, A.D. Sherry, Angew. Chem. Int.Ed., 2003, 42, 5889.
[126] S. Zhang, R. Trokowski, A.D. Sherry, J. Am. Chem. Soc., 2003, 125, 15288.
[127] J.- C. G. Bünzli, C. Piguet, Chem. Rev., 2002, 102, 1897.
[128] N. Sabbatini, M. Guargigli, I. Manet, R. Ungaro, A. Casnati, R.Ziessel, G. Ulrich, Z. Asfari, J.-M. Lehn, Pure Appl. Chem., 1995, 67, 135.
[129] M.P. Oude Wolbers, F.C.J.M. van Veggel, B.H.M. Snellick-Ruel,J.W. Hofstraat, F.A.J. Guerts, D.N. Reinhoudt, J. Am. Chem. Soc, 1997,119,138.
[130] J. Huskens, J.A. Peters, H. Van Bekkum, Inorg. Chem., 1995, 34,1756.
[131] D. Parker, J.A.G. Williams, J. Chem. Soc, Dalton Trans., 1996, 3613.
[132]S. E.Matthews, C.W.Pouton, M.D.Threadgill, Adv. Drug Delivery Rev., 1996,18,219.
[133] D. Parker, Coord. Chem. Rev, 2000,205,109; Goddard III, J. Am. Chem. Soc, 1999, 121,6142.
[134] D. Parker, R.S. Dickins, H. Purschmann, C. Crossland, J.A.K.Howard, Chem. Rev, 2002,102,1977.
[135] Y. Bretonniere, M. Mazzanti, R. Wietzke, J. Pecaut, Chem. Commun, 2000,1543.
[136] J.-C.G. Bunzli, N. Andre, M. Elhabiri, G. Muller, C. Piguet, J.Alloys Compd, 2000,66, 303.
[137] C. Piguet, C. Edder, H. Nozary, F. Renaud, S. Rigault, J.-C.G.Bunzli, J. Alloys Compd, 2000,94,303.
[138] T.Gunnlaugsson, D.A.Mac D'onaill, D.Parker, J.Am.Chem. Soc, 2001,123,12866.
[139] C.M. Rudzinski, A.M. Young, D.G. Nocera, J. Am. Chem. Soc, 2002,124,1723.
[140] Y. Bretonni' ere, M.J. Cann, D. Parker, R. Slater, Chem. Commun, 2002,1930.
[141] P. Atkinson, Y. Bretonniere, D. Parker, Chem. Commun, 2004,438.
[142] D. Parker, Chem. Soc. Rev, 2004,33,156.
[143] E. Tdth, L. Helm, A.E. Merbach, in: J.A. McCleverty, T.J. Meyer(Eds.), Comprehensive Coordination Chemistry II, vol. 9, Elsevier, 2004, Chapter 19.
[144] (a) R.B. Lauffer, Chem. Rev, 1987, 87, 901; (b) P. Caravan, J.J. Ellison, T.J. McMurry, R.B. Lauffer, Chem. Rev, 1999, 99,2293.
[145] S. Zhang, K. Wu, A.D. Sherry, Angew. Chem. Int. Ed, 1999,38,3192.
[146] V. Comblin, D. Gilsoul, M. Hermann, V. Humblet, V. Jacques, M.Mesbahi, C. Sauvage, J.F. Desreux, Coord. Chem. Rev, 1999,451,185.
[147] J.P. Andre, E. Tdth, H. Fischer, A. Seelig, H.R. M¨acke, A.E. Merbach, Chem. Eur. J, 1999,5,2977.
[148] M. Woods, S. Aime, M. Botta, J.A.K. Howard, J.M. Moloney, M.Navet, D. Parker, M. Port, O. Rousseaux, J. Am. Chem. Soc, 2000,122, 9781.
[149] M. Botta, Eur. J. Inorg. Chem, 2000, 399.
[150] F.A. Dunand, R.S. Dickins, D. Parker, A. Merbach, Chem. Eur. J, 2001,7,5160.
[151] S.Aime, D.D.Castelli, F. Fedeli, E. Terreno, J. Am. Chem. Soc, 2002,124,9364.
[152] W. Li, G.Parigi, M.Fragai, C.Luchinat, T.J. Meade, Inorg. Chem, 2002,41,4018.
[153] M.Woods, Z. Kovacs, S. Zhang, A.D. Sherry, Angew. Chem. Int.Ed, 2003,42,5889.
[154] S. Zhang, R. Trokowski, A.D. Sherry, J. Am. Chem. Soc, 2003,125,15288.
[155] F. Yerly, A. Borel, L. Helm, A.E. Merbach, Chem. Eur. J, 2003,9, 5468.
[156] L.V. Elst, M. Port, I. Raynal, C. Simonot, R.N. Muller, Eur.J.Inorg. Chem., 2003, 2495.
[157] K. Kimpe, T.N. Parac-Vogt, S. Laurent, C. Pierart, L.V. Elst, R.N.Muller, K. Binnemans, Eur. J. Inorg. Chem., 2003, 3021.
[158] S. Jurisson, D. Berning, W. Jia, D. Ma, Chem. Rev., 1993, 93,1137.
[159] Y.H. Jang, M. Blanco, S. Dasgupta, D.A. Keire, J.E. Shively, W.A.Goddard III, J. Am. Chem. Soc, 1999,121,6142.
[160] H. Ali, J. E. Van Lier, Chem. Rev., 1999,99,2379.
[161] D.A. Keire, Y.H. Jang, L. Li, S. Dasgupta, W.A. Goddard III, J.E.Shively, Inorg. Chem., 2001,40,4310.
[162] J.L. Sessler, T.D. Mody, G.W. Hemmi, V. Lynch, S.W. Young, R.A.Miller, J. Am. Chem. Soc, 1993,115,10368.
[163] S.W.A. Bligh, N. Choi, C.F.G.C. Geraldes, S. Knoke, M. Mc-Partlin, M.J. Sanganee, T.M. Woodroffe, J. Chem. Soc, DaltonTrans., 1997,4119.
[164] L. Thunus, R. Lejeune, Coord. Chem. Rev. 1999,184,125.
[165] K. Wang, R. Li, Y. Cheng, B. Zhu, Coord. Chem. Rev., 1999,297,190.
[166] D. Kong, L. Meng, L. Song, Y. Xie, Transition Met. Chem., 1999,24,553.
[167] J.L. Sessler, R.A. Miller, Biochem. Pharmacol., 2000, 59, 733.
[168] L.A.D. Williams, R.C. Howell, R. Young, I.A. Kahwa, Comp.Biochem. Physiol. Part C: Toxicol. Pharmacol., 2001,128,119.
[169] M. Woods, Z. Kovacs, A.D. Sherry, J. Supramolecular Chem., 2002,2,1.
[170] R.W. Hay, N. Govan, J. Chem. Soc, Chem. Commun., 1990,714.
[171] J.R. Morrow, L.A. Buttery, V.M. Shelton, K.A. Berback, J. Am.Chem. Soc, 1992,114, 1903.
[172] N. Hayashi, N. Takeda, T. Shiiba, M. Yashiro, K. Watanabe, M.Komiyama, Inorg. Chem., 1993,32, 5889.
[173] J. K. Bashkin, L.A. Jenkins, Comments Inorg. Chem., 1994,16, 77.
[174] B. K. Takasaki, J. Chin, J. Am. Chem. Soc, 1994,116,1121.
[175] K. Matsumura, M. Endo, M. Komiyama, J. Chem. Soc, Chem. Commun., 1994,2019.
[176] D. Magda, R.A. Miller, J.L. Sessler, B.L. Iverson, J. Am. Chem.Soc, 1994,116,7439.
[177] K. G. Ragunathan, H.-J. Schneider, Angew. Chem. Int. Ed., 1996,35,1219.
[178] R. Haner, J. Hall, Antisense Nucl. Acid Drug Dev., 1997,7,423.
[179] B.F. Baker, H. Khalili, N. Wei, J.R. Morrow, J. Am. Chem. Soc, 1997,19, 8749.
[180] P.E. Jurek, A.E. Martell, Chem. Commun., 1999,1609.
[181] B.F. Baker, S.S. Lot, J. Kringel, S. Cheng-Flournoy, P. Villiet, H.M.Sasmor, A.M. Siwkowski, L.L. Chappell, J.R. Morrow, Nucl. Acids Res., 1999,27,1547.
[182] D.M. Epstein, L.L. Chappell, H. Khalili, R.M. Supkowski, W.DeW.Horrocks Jr., J.R. Morrow, Inorg. Chem., 2000, 39,2130.
[183] S.J. Franklin, Curr. Opin. Chem. Biol., 2001,5,201.
[184] S.W.A. Bligh, N. Choi, E.G. Evagorou, M. McPartlin, K.N. White,J. Chem. Soc, Dalton Trans., 2001, 3169.
[185] C. Liu, M. Wang, T. Zhang, H. Sun, Coord. Chem. Rev., 2004,248,147.
[186] C. H. Evans, in: E. Frieden (Ed.), Biochemistry of Lanthanides, Plenum Press, New York, 1990, Chapter 9.
[187] J.-C.G. B¨unzli, in: K.A. Gschneidner Jr., L. Eyring (Eds.), Handbookon the Physics and Chemistry of Rare Earths, vol. 9, Elsevier, Amsterdam, 1987, Chapter 60.
[188] M.F. Tweedle, in: J.-C.G. Bunzli, G.R. Choppin (Eds.), LanthanideProbes in Life, Chemical and Earth Sciences, Elsevier, Amsterdam, 1989, Chapter 5.
[189] H. Tsukube, S. Shinoda, Chem. Rev., 2002,102,2389.
[190] P.H. Brown, A.H. Rathjen, R.D. Graham, D.E. Tribe, in: K.A.Gschneidner Jr., L. Eyring (Eds.), Handbook on Physics and Chemistryof Rare Earths, vol. 13, Elsevier Science Publishers, Amsterdam,1990, Chapter 92.
[191] J.R. Duffield, D.M. Taylor, D.R. Williams, in: K.A. GschneidnerJr., L. Eyring, G.R. Choppin, G.H. Lander (Eds.), Handbook onPhysics and Chemistry of Rare Earths, vol. 18, Elsevier Science Publishers, Amsterdam, 1994, Chapter 129.
[192] J.M. Harrowfield, M.I. Ogden, R. Richmond, A.H. White, J. Chem.Soc, Dalton Trans., 1991,2153.
[193] W. Radecka-Paryzek, Inorg. Chim. Acta, 1979,35,349.
[194] W. Radecka-Paryzek, Inorg. Chim. Acta, 1979,34,5.
[195] W. Radecka-Paryzek, Inorg. Chim. Acta, 1981, 52 261.
[196] W. Radecka-Paryzek, Polyhedron, 1989, 8,1217.
[197] W. Radecka-Paryzek, E. Luks, Polyhedron, 1994, 13, 899.
[198] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, Pol. J. Chem., 1995, 69,1.
[199] J. Cai, J.G. Muller, C.J. Burrows, Supramol. Chem., 2002,14,121.
[200] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, Polyhedron, 1995,14,2059.
[201] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, Collect. Czech.Chem. Commun., 1998,63,363.
[202] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, H. Litkowska, Polyhedron, 1998, 17,1477.
[203] W. Radecka-Paryzek, H. Litkowska, J. Alloys Compd., 2000,435,300.
[204] W. Radecka-Paryzek, V. Patroniak, M. Kubicki, Polyhedron, 2003,22,2773.
[205] W.Radecka-Paryzek, V.Patroniak, M.Kubicki, Inorg. Chem. Commun., 2004, 7,455.
[206] V. Patroniak, M. Kubicki, A. Mondry, J. Lisowski, W. Radecka-Paryzek, Dalton Trans., 2004,3295.
[207] W. Radecka-Paryzek, Inorg. Chim. Acta, 1980,45,147.
[208] L.M.J. Vallarino, in: K.A. Gschneidner Jr., L. Eyring (Eds.), Handbookon the Physics and Chemistry of Rare Earths, vol. 15, Elsevier,Amsterdam, 1991, Chapter 104.
[209] A.M. Arif, J.D.J. Backer-Dirks, C.J. Gray, F.A. Hart, M.B. Hursthouse,J. Chem. Soc., Dalton Trans., 1987,1665.
[210] (a) L. De Cola, D.L. Smailes, L.M. Vallarino, Inorg. Chem., 1986,25,1729; (b) K.K. Fonda, L.M. Vallarino, Inorg. Chim. Acta, 2002, 334,403.
[211] G. Bombieri, J. Alloys Compd., 1997,249, 76.
[212] T.W. Bell, F. Guzzo, M.G.B. Drew, J. Am. Chem. Soc, 1991,113, 3121.
[213] J.R. Morrow, L.A. Buttery, V.M. Shelton, K.A. Berback, J.Am.Chem.Soc, 1992,114, 1903.
[214] N. Hayashi, N. Takeda, T. Shiiba, M. Yashiro, K. Watanabe, M.Komiyama, Inorg. Chem, 1993,32,5889.
[215] D.A. Voss Jr., L.A. Buttrey-Thomas, T.S. Janik, M.R. Churchill,J.R. Morrow, Inorg. Chim. Acta, 2001, 317,149.
[216] L. M. Vallarino, J. Alloys Compd., 1997,249,69.
[217] (a)F. Benetollo, G. Bombieri, W.A. Gootee, K.K. Fonda, K.M.Samaria, L.M. Vallarino, Polyhedron, 1998,17, 3633; (b) F. Benetollo, G. Bombieri, A.M. Adeyga, K.K. Fonda, W.A.Gootee, K.M. Samaria, L.M. Vallarino, Polyhedron, 2002,21,425.
[218] S. Kobayashi, T. Hamada, S. Nagayama, K. Manabe, Org. Lett, 2001,3,165.
[219] T. Hamada, K. Manabe, S. Ishikawa, S. Nagayama, M. Shiro, S.Kobayashi, J. Am. Chem. Soc, 2003, 125,2989.
[220] T. Tsubomura, K. Yasaku, T. Sato, M. Morita, Inorg. Chem, 1992,31,447.
[221] S.W.A. Bligh, N. Choi, E.G. Evagorou, W.-S. Li, M. McPartlin,Chem. Commun, 1994, 2399.
[222] A. Lachgar, K.S. Coates, S.C. Jackels, Inorg. Chem, 1994,33,2219.
[223] L.H. Bryant Jr., A. Lachgar, S.C. Jackels, Inorg. Chem., 1995,34,4230.
[224] J. Lisowski, P. Starynowicz, Polyhedron, 2000,19,465.
[225] J. Lisowski, P. Starynowicz, Inorg. Chem. Commun., 2003,6, 593.
[226] J. Mazurek, J. Lisowski, Polyhedron, 2003,22,2877.
[227] N.H. Pilkington, R. Robson, Aust. J. Chem., 1970,23,2225.
[228] H. Okawa, S. Kida, Bull. Chem. Soc. Jpn., 1972,45, 1759.
[229] B. F. Hoskins, R. Robson, G.A. Williams, Inorg. Chim. Acta, 1976,16,121.
[230] L.K. Thompson, S. K. Mandal, S.T. Tandon, J.N. Bridson, M.K.Park, Inorg. Chem., 1996,35,3117.
[231] A. Asokan, B. Varghese, A. Caneschi, P.T. Manoharan, Inorg.Chem., 1998, 37,228.
[232] H. Wada, K. Motoda, M. Ohba, H. Sakiyama, N. Matsumoto, H.~-Okawa, Bull. Chem. Soc. Jpn., 1995,68,1105.
[233] H.-R. Chang, S.K. Larsen, P.D.W. Boyd, C.G. Pierpont, D.N. Hendrickson ,J. Am. Chem. Soc, 1988,110,4565.
[234] R.R. Gagne, C.L. Spiro, T.J. Smith, C.A. Hamann, W.R. Thies,A.K. Shiemke, J. Am. Chem. Soc, 1981,103,4073.
[235] S.K. Dutta, J. Ensling, R. Werner, U. Florke, W. Haase, P. Gutlich,K. Nag, Angew. Chem. Int. Ed., 1997,36,152.
[236] A. Asokan, B. Varghese, A. Caneschi, P.T. Manoharan, Inorg. Chem., 1998,37,228.
[237] A.J. Atkins, A.J. Blake, M. Schroder, J. Chem. Soc, Chem. Commun., 1993,353.
[238] A.J. Atkins, D. Black, A.J. Blake, A. Marin-Becerra, L. Ruiz-Ramirez, M. Schroder, J. Chem. Soc, Chem. Commun., 1996,457.
[239] A.J. Atkins, D. Black, R.L. Finn, A. Marin-Becerra, A.J. Blake,L. Ruiz-Ramirez, W.-S. Li, M. Scr¨oder, Dalton Trans., 2003,1730.
[240] B. Dutta, B. Adhikary, P. Bag, U. F16rke, K. Nag, J. Chem. Soc,Dalton Trans., 2002, 2760.
[241] P. Starynowicz, J. Lisowski, Chem. Commun., 1999,769.
[242] M. Tadakoro, H. Sakiyama, N. Matsumoto, M. Kodera, H. Okawa,J. Chem. Soc, Dalton Trans., 1992,313.
[243] S. S. Tandon, V. McKee, J. Chem. Soc, Dalton Trans., 1989,19.
[244] N.A. Bailey, D.E. Fenton, P.B. Roberts, A.M. Walford, J. Chem.Soc, Dalton Trans., 1987,1865.
[245] M. Botta, U. Casellato, C. Scalco, S. Tamburini, P. Tomasin, P.A. Vigato, S. Aime, A. Barge, Chem. Eur. J., 2002, 8,3917.
[246] A. Caneschi, L. Sorace, U. Casellato, P. Tomasin, P.A. Vigato, Eur. J. Inorg. Chem., 2004, 3887.
[247] M. Sakamoto, K. Manaseki, H. (?)kawa, Coord. Chem. Rev., 2001, 379, 219.
[248] J. Lisowski, P. Starynowicz, Inorg. Chem., 1999, 38, 1351.
[249] J. Lisowski, P. Starynowicz, Polyhedron, 1999, 18, 443.
[250] J. Lisowski, Unpublished results.
[251] S.S. Tandon, L.K. Thompson, J.N. Bridson, Chem. Commun., 1992, 911; S.S. Tandon, L.K. Thompson, J.N. Bridson, C. Benelli, Inorg.Chem., 1995, 34, 5507.
[252] F.Avecilla, R.Bastida, A. De Bias, D.E. Fenton, A.Mayas, A.Rodryguez, T. Rodryguez-Blas, S.Garcia-G-randa, R Corzo-Suarez, J. Chem. Soc.,Dalton Trans., 1997, 409.
[253] F. Avecilla, A. De Bias, R. Bastida, D.E. Fenton, J. Mah'ya, A.Mac'yas, C. Platas, A. Rodr'yguez, T. Rodr'yguez-Blas, Chem. Commun., 1999, 125.
[254] Q. Zeng, S. Gou, L. He, Y. Gong, X. You, Inorg. Chim. Acta, 1999, 287, 14.
[255] C. Platas, F. Avecilla, A. De Bias, C.F.G.C. Geraldes, T. Roddguez-Blas, H. Adams, J. Mahia, Inorg. Chem., 1999, 38, 3190.
[256] Q.-Y. Chen, Q.-H. Luo, Z.-L. Wang, J.-T. Chen, Chem. Commun., 2000, 1033.
[257] Q.-Y. Chen, Q.-H. Luo, D.-G. Fu, J.-T. Chert, J. Chem. Sot., Dalton Trans., 2002, 2873.
[258] X.-L. Hu, M.-C. Shen, J.-T. Chen, Chem. Eur. J., 2002, 8, 3984.
[259] F. Avecilla, C. Platas-Iglesias, R. Rodryguez-Cortinas, G. Guillemont,J.-C.G. Bünzli, C.D. Brondino, C.F.G.C. Geraldes, A. DeBlas, T. Rodryguez-Blas, J. Chem. Soc., Dalton Trans., 2002, 4658.
[260] R. Rodryguez-Corti(?)as, F. Avecilla, C. Platas-Iglesias, D. Imbert,J.-C.G. Bünzli, A. De Bias, T. Rodr'yguez-Blas, Inorg. Chem., 2002, 41, 5336.
[261] Q.-Y. Chen, Q.-H. Luo, L.-M. Zheng, Z.-L. Wang, J.-T. Chen, Inorg. Chem., 2002, 41,605.
[262] S.R. Korupoju, N. Mangayarkarasi, S. Ameerunisha, E.J. Valente,P.S. Zacharias, J. Chem. Soc., Dalton Trans., 2000, 2845.
[263] S.R. Korupoju, N. Mangayarkarasi, P.S. Zacharias, J. Mizuthani,H. Nishihara, Inorg. Chem., 2002, 41, 4099.
[264] N. Kuhnert, G.M. Rossignolo, A.Lopez-Periago, Org. Biomol.Chem., 2003, 1, 1157.
[265] N.Raman, A.Kulandaisamy, A. Shunmugasundaram, K. Jeyasubramanian, Transition Met. Chem., 2001, 26, 131.
[266] R. S. Srivastava, Inorg. Chim. Acta., 1981, 56, 65.
[267] N. Gupta, R. Swaroop, R. V. Singh, Main Group Met. Chem., 1997, 14, 387.
[268] (a) L. Mishra, V. K. Singh, Indian J. Chem., 1997, 32A, 446; (b) R. Malhotra, S. Kumar, Dhindsa, K. S. Indian, J. Chem., 1993, 32A, 457; (c) W. Levinson, E. Jawetz, Med. Microbiol. Immunol., 4th edit., Stamford, 1996.
[269] H. Smit, et al., Antimicrobial Agents and Chenetherapy, 1982, 21,881
[270] B. M. Aritic, et al., Europ. J. Med. Chem., 1977,12, 573
[271] E. M. Hodnett, W. J. J. Dunn, Med. Chem. 1970, 13, 768.
[272] 陈德余，张义建，张平等，应用化学，2000，17，607
[273] 张建民，李瑞芳，无机化学学报，1999，15，493
[274] 叶勇．湖北大学学报，2001，23，57．
[275] T. R. Younkin, E. F. Connor, R. H. Grubbs, et al., Sc., 2000, 287, 460
[276] S. Matsui, T. Fujita, Catalysis Today, 2001, 66, 63
[277] L. K. Johnson, C. M. Killian, M. Brookhart, et al., J. Am. Chem.Soc.,1995, 117, 6415
[278] Small B L, Brookhart M, Bennett A M A, et al., J Am. Chem.Soc., 1998, 120, 4049
[279] Britovsek G J P, Bruce M,Gibson V C, et al., J Am. Chem.Soc., 1999, 121, 8727
[280] B. L. Small, M. Brookhart, J. Am. Chem.Soc., 1998, 120, 7143
[281] L. S. Cai, H. Mahmoun, Y. Han, Tetrahedron: Asymmetry, 1999, 10, 411.
[282] 仇敏，刘国生，姚小泉等，催化学报，2001，22，77．
[283] 李琛，张维萍，姚小泉等．催化学报，2000，21，289．
[284] Z.G. Li, Z. Zhuo, B.S.Wan, et al., Journal of molecular Catalysis A: Chemical, 2001, 165, 67.
[285] H.-W. Wang, W. Sun, C.-G. Xiao, J. Mol. Catal. A: Chem., 2003, 206, 199.
[286] Z.-N Li, G.-S. Liu, Z. Zheng, et al., Tetrahedron, 2002, 56, 7187.
[287] L. J. Therior, G. O. Carlisle, H. J. Hu, J. Inorg. Nucl. Chem., 1969, 31, 2841
[288] 彭清静，傅伟吕，邹晓勇等，化学世界，2001，10，539．
[289] 范谦，黎耀忠，程克梅等，四川大学学报(自然科学版)，2001，38，230．
[290] H. Ma, S.-H. Chen, L. J. Niu, Electrochem. Soc., 2001, 148, 208.
[291] 李晓常，孙景志，马於光，高等学校化学学报，1999，20，309。
[292] X.-Z.You, W.-H.Feng, J. Chem. Soc. Chem. Commun., 1994, 2391.
[293] 田颜清，林凤，赵英英等，应用化学，1993，12，90。
[294] 程鹏，廖代正，阎世平等，中国科学(B辑)，1996，26，97。
[295] D. B. Wang, B. H. Chen, Y. X. Ma, Syn. React. Inorg. Met.-Org. Chem., 1997, 27, 479.
[296] Z. H. Chohan, A. Rauf, Syn. React. Inorg. Met.-Org. Chem., 1996, 26, 591.
[1] Bruker, SMART (Version 5.628) and SAINT (Version 6.02). Bruker AXS Inc., Madison, Wisconsin, USA., 1998.
[2] G. M. Sheldrick, SADABS. Program for Multi-scan Absorption Correction of Area Detector, University of G(?)ttingen, Germ., 1996.
[3] G. M. Sheldrick, SHELXTL V5.1 Software Reference Manual, Bruker AXS, Inc., Madison, Wisconsin, USA., 1997.
[4] X. Chen, C. Plasencia, Y. Hou, N. Neamati, J. Med. Chem. 2005, 48, 1098.
[5] H.-Q. Li, H.-M. Ge, Y.-X.i Chen, L. Shi, H. Ding, H.-L. Zhu, and R.-X. Tan, Chem. Biodivers., 2006, 3,463.
[1] Paola V., Matteo I., Irini A. D., Paolo L. C., Bernadetta B., Roberta L., Eur. J. Med. Chem., 2006, 41,624..
[2] Timothy B. Chaston, Des R. Richardson, J Biol Inorg Chem, 2003, 8, 427.
[3] Patricia M., Virginie L., Christian S., and Philippe G., Bioorg. & Med. Chem. Let., 2006, 16,31.
[4] Rosanna Maccari, Rosaria Ottana and Mafia Gabriella Vigorita, Bioorg. & Med. Chem. Let., 2005, 15, 2509.
[5] Dharmarajan Sriram, Perumal Yogeeswari and Kasinathan Madhu, Bioorg. & Med. Chem. Let., 2006, 16, 876.
[6] Rando D.G., Doriguetto A.C., Tomich de Paula da Silva C.H., Ellena J., Sato D.N. Leite,C.Q.F., Varanda E. A., Ferreira E.I., Eur. J. Med. Chem., 2006, 41, 1196.
[7] Bao-dui Wang, Zheng-Yin Yang and Tian-rong Li, Bioorg. & Med. Chem. Let. 2006, 14, 6012.
[8] Xu C., Mao H. Y., Zhang H. Y., Liu H. L., J. Mol. Struct., 2003, 658, 59.
[9] P. Melnyk, V. Leroux, C. Sergheraert, P. Grellier, Bioorg. Med. Chem.Lett., 2006, 16, 31.
[10] D.G. Rando, D.N. Sato, L. Siqueira, A. Malvezzi, C.Q.F. Leite, A.T. Amaral, E.I. Ferreira, L.C. Tavares, Bioorg. Med. Chem., 2002, 10, 557.
[11] J. Patole, U. Sandbhor, S. Padhye, D.N. Deobagkar, C.E. Anson, A.Powell, Bioorg. Med. Chem. Lett., 2003, 13, 51.
[12] R. Maccari, R. Ottana, M.G. Vigorita, Bioorg. Med. Chem. Lett., 2005, 15, 2509.
[13] N. Georgieval and V. Gadjeva, Biochemistry-moscow+,, 2002, 67, 705.
[14] E.M. Sah., D.J. Drain, M. Seiler, J. Pharm. Pharmacol. 1952, 4, 844.
[15] S. Rollas, N. Gu¨lerman, H. Erdeniz, Farmaco, 2002, 57, 171.
[16] S. Güniz Kücükgüzel, Adil Mazi, Fikrettin Sahin, Suzan (?)ztürk, James Stables, Eur. J. Med. Chem., 2002, 37, 197.
[17] S. Güniz Kücükgüzel, Adil Mazi, Fikrettin Sahin, Suzan (?)ztürk, James Stables, Eur. J. Med. Chem., 2003, 38, 1005.
[18] X. Chen, C. Plasencia, Y. Hou, N. Neamati, J. Med. Chem., 2005, 48, 1098.
[1] T.R. Frieden, T. R. Sterling, S. S.Munsi., C. J. Watt, C. Dye, Lancet, 2003, 362, 887.
[2] C. S. Currie, B. G. Williams, R. C. Cheng, C. Dye, AIDS, 2003, 17, 2508.
[3] B. G. Williams, C. Dye, Sci., 2003, 301, 1537.
[4] Z. Toossi, H. Mayanja-Kizza, C. S. Hirsch, K. L.Edmonds, T. Spahlinger, D. L. Hom, H. Aung, P. Mugyenyi, J. J. Ellner, C. W.C. Whalen., Exp. Immunol, 2001, 123, 8.
[5] J. A. Sbarbaro, Chest 1997, 111, 1151.
[6] R.J. Coker, Public Health, 2003, 117, 281.
[7] P. S. J. Floriano, E. Javier, L. F. Marcelle de., Y. P. Mascarenhas, M. V.N. de Souza, T. R.A. Vasconcelos, J. L. Wardell, S. M.S.V. Wardell, J. Mol. Struct., 2006, 788, 63.
[8] I. A. Blair, R. M. Timoco, M. J. Brodie, R. A. Clare, T. Dollery, J. A Timbrell, I. A.Beever Hum., Toxicol., 1985, 4, 202.
[9] G. L. Mondell, M. A. Sande, In The Pharmacological Basis of Therapeutics, A. G.Gilman, T. W.Rull, Eds., 8th ed.; Pergamon Press: New York, 1991, p1147.
[10] W. J. Wechter, M. A. Johnson, C. M. Hall, D. T. Warner, A. E. Berger, A. H. Wenzel, D. T.Gish, G. L. Neil, J. Med. Chem., 1975, 18, 344.
[11] R. Maccari, R. Ottana, F. Monforte, M. G. Vigorita Antimicrob, Agent Chemother., 2002, 46, 294.
[12] E. Szarvasi, L. Fontaine, A. Betbeder-Matibet, J. Med. Chem., 1973, 16, 281.
[13] H.M. Eisa, A.S. Tantawy, M.M. El-Kerdawy, Pharmazie, 1991, 46, 182.
[14] M.A. Khalil, O.A. El-Sayed, H.A. El-Shamy, Arch. Pharm., 1991,182. 4 N. Ulusoy, G. C, apan, G. ou tu k, M. Kiraz, Boll. Chim., Farmac, 2000,139,167.
[15] N. Ulusoy, N. Ergenc, G.o tuk, M. Kiraz, Boll. Chim., Farmac, 2001,140,417.
[16] S. Rollas, N. Gulerman, H. Erdeniz, Farmaco, 2002, 57,171.
[17] S.G. Kuc.ukgu zel, E.E. Oruc, S. Rollas, F. Sahin, A. ozbek, Eur. J. Med. Chem., 2002, 37,197.
[18] N. Ulusoy, N. Ergenc,, A.C. Ekinci, H. o zer, Monatsh. Chem., 1996, 127,1197.
[19] B.C.akir, E. Yildirim, T. Ercanli, K. Erol, M.F. Sahin, Farmaco, 1999, 54, 842.
[20] J.R. Dimmock, S.C. Vashishtha, J.P. Stables, Eur. J. Med. Chem, 2000, 35,241.
[21] S.N.Pandeya, H. Manjula, J.P. Stables, Pharmazie, 2001, 56,121.
[22] E.M. Sah., D.J.Drain, M. Seiler, J. Pharm. Pharmacol, 1952,4, 844.
[23] J.M. Patel, M.P. Dave, N.A. Langalia, K.A. Thaker, J. Indian Chem. Soc, 1984,61,718.
[24] L. Bukowski, M. Janowiec, Pharmazie, 1996,51,27.
[25] S.G. K c.ukgu zel, S. Rollas, I. Kuc.ukgu zel, M. Kiraz, Eur. J Med. Chem., 34,1999,1093.
[26] L. Bukowski, M. Janowiec, Z. Zwolska-Kwiek, Z. Andrzejczyk, Pharmazie, 1999,54,651.
[27] Joshi C., Khosla N., Tiwari P. Bioorg., Med. Chem., 2004,14,571.
[28] D. Sriram, P. Yogeeswari and K. Madhu Bioorg. & Med. Chem. Lett., 2005,15,4502.
[29] H. Smit,et al., Antimicrob. Agents Ch., 1982,21, 881
[30] B. M. Aritic, et al, Europ. J. Med. Chem., 1977,12, 573
[31] N.Gupta, R. Swaroop, R. V. Singh, Main Group Met. Chem., 1997,14,387.
[32] L.Mishra, V. K. Singh, Indian J Chem, 1997,32A, 446.
[33] R. Malhotra, S. Kumar, K. S. Dhindsa, Indian J. Chem, 1993,32A, 457.
[34] W. Levinson, E. Jawetz, Med. Microbiol. Immun, 4th edit, Stamford, 1996.
[1] S.Adsule, V. Barve, D. Chen, F.Ahmed, Q. P.Dou, S. Padhye, F.H. Sarkar, J. Med. Chem., 2006; 49(24), 7242-7246.
[2] T. Ota, Y. Furutani, A. Terakita, Y. Shichida, H. Kandod, Biochem. 2006; 45(9), 2845-2851.
[3] M. Shibata, H. Kandori, Biochemistry, 2005, 44(20), 7406-7413.
[4] B. Thati, A. Noble, B. S. Creaven, M. Walsh, M. McCann, K. Kavanagh, M. Devereux, D. A. Egan, Cancer Letters, 2007, 248, 321-331
[5] D. Sriram, E Yogeeswad and R. V. Devakaram, Bioorg. Med. Chem., 2006, 14, 3113-3118.
[6] R. Herchel, R. Boca, M. Gembicky, K. Falk, H. Fuess, W. Haase, I. Svoboda, Inorg. Chem., 2007; 46(5); 1544-1546.
[7] T. Tanaka, Y.Yasuda, M. Hayashi, J. Org. Chem. 2006; 71(18), 7091-7093.
[8] R.Herchel, R. Boca, M. Gembicky, K. Falk, H. Fuess, W. Haase, I. Svoboda, Inorg. Chem., 2007; 46(5), 1544-1546.
[9] S. Handa, V. Gnanadesikan, S. Matsunaga, M. Shibasaki, J. Am. Chem. Soc., 2007, 129(16), 4900-4901.
[10] E. R. Jarvo, B. M. Lawrence, E. N. Jacobsen, Angew. Chem., 2005, 117, 6197-6200
[11] M. Zhao, C. Zhong, C. Stem, A. G. M. Barrett, B. M. Hoffman, J. Am. Chem. Soc., 2005; 127(27), 9769-9775.
[12] E. Jabri, M. B. Carr, R. P.Hausinger, et al. Sci., 1995, 268, 998.
[13] Z.-L. You, H.-L. Zhu, Z. Anorg. Allg. Chem., 2006, 632, 140.
[14] A. Panja, N. Shaikh, S. Gupta, R. J. Butcher, P. Banerjee, Eur. J. Inorg. Chem., 2003, 1540.
[15] H.-L. Zhu, Y.-X. Tong, X.-M. Chen, J. Chem. Soc., Dalton Trans., 2000, 4182.
[16] 肖子敬，刘世雄，林墀昌，无机化学学报，2004，20，513。
[17] Gupta, N., Swaroop, R., Singh, R. V. Main Group Met. Chem., 1997, 14, 387.
[18] (a) L. Mishra, V. K. Singh, Indian J. Chem., 1997, 32A, 446; (b) R. Malhotra,, S. Kumar, K. S. Dhindsa, Indian J. Chem., 1993, 32A, 457; (c) W. Levinson, E. Jawetz, Med.1 Microbiol. Immunol., 4th edit., Stamford, 1996.
[19] H. Smit, et al., Antimicrob. Agents Ch., 1982, 21,881
[20] B. M. Aritic, et al., Europ. J. Med. Chem., 1977, 12, 573
[1] T. Tanaka, Y. Yasuda, M. J. Hayashi, Org. Chem., 2006, 71(18), 7091-7093.
[2] Y. L. Qian, W. Zhao, J. L. Huang, Inorg. Chem. Commun. 2004, 7, 459.
[3] M. B. Ferrari, F. Bisceglie, G. Reffo, G.. Pelosi, P. Tarasconi, R. Albertini, A. Bonati, P. Lunghi, S. J. Pinelli, Inorg. Biochem., 2001, 83, 169.
[4] A. Okada, T. Shibuguchi, T. Ohshima, H. Masu, K. Yamaguchi, M. Shibasaki Angew. Chem. Intern. Ed., 2005, 44(29), 4564-4567.
[5] J. Ziegler, T. Schuerle, L. Pasierb, C. Kelly, A. Elamin, K. A. Cole, D. W. Wright, Inorg. Chem.; 2000, 39(16), 3731-3733.
[6] S. Adsule, V. Barve, D. Chen, F. Ahmed, Q. P. Dou, S. Padhye, F. H. Sarkar, J. Med. Chem., (Brief Article), 2006, 49(24), 7242-7246.
[7] M. Alexiou,; I. Tsivikas, C. Dendrinou-Samara, A. A. Pantazaki, P. Trikalitis, N. Lalioti, D. A. Kyriakidis, D. P. J. Kessissoglou, Inorg. Biochem., 2003, 93, 256.
[8] H. Zahid, M. Chohan, M. Arif, Appl. Organomet. Chem., 2007, 21(4), 294-302.
[9] F. M. Belicchi, F. Bisceglie, G.. Pelosi, M. Sassi, P. Tarasconi, M. Cornia, S. Capacchi, R. Albertini, S. Pinelli, J. Inorg. Biochem., 2002, 90, 113.
[10] R. Campo, J. J. Criado, E. Garcia, M. R. Hermosa, A. Jimenez-Sanchez,; J. L. Manzano, E. Rodriguez-Fernandez, F. Sanz, J. Inorg. Biochem., 2002, 89, 74.
[11] Alexiou, M.; Tsivikas, I.; Dendrinou-Samara, C.; Pantazaki, A. A.; Trikalitis, P.; Lalioti, N.; Kyriakidis, D. A.; Kessissoglou, D. P. J. Inorg. Biochem., 2003, 93, 256.
[12] S.-X. Liu, S. Lin, B.-Z. Lin, C.-C. Lin, J.-Q. Huang, 2001, Angew. Chem., Int. Ed. Engl., 40, 1084
[13] Xiao-Hua Chen, Shi-Xiong Liu Chin. J. Inorg. Chem., 2005, 21,15
[14] J.-L. Hou, X.-B. Shao, G-J. Chen, Y-X. Zhou, X.-K. Jing, Z.-T. Li, J. Am. Chem. Soc., 2004, 126, 12386.
[15] H. Smit, et al., Antimicrob. Agents Ch., 1982, 21, 881
[16] W. Levinson, E. Jawetz, Med. Microbiol. Immun., 4th edit., Stamford, 1996.
[17] S. B. Charles, M. Lesley, P. Lynn, J. D. Susan, Biochim. Biophys. Acta., 2005, 1740, 340.
[18] K. A. Irena, M. B. Georgi, Z. B. Maya, K. Margarita, Euro. J. Med., 2005, 40, 542.
[19] X. Zhong, J. Yi, J. Sun, H.-L. Wei, W.-S. Liu, K.-B. Yu, Eur. J. Med. Chem., 2006, 41, 1090.
[1] Y.-P. Tian, C.-Y. Duan, X.-Z. You, Transit. Met. Chem., 1998, 23, 17.
[2] X. H. Zhu, S. H. Liu, Y. J. Liu, J. Ma, C. Y. Duan, X. Z. You, Y. P. Tian, F. X. Xie, S. S. Ni, Polyhedron, 1998, 19, 181
[3] M. A. Ali, S. M. M. H. Majumder, R. J. Butcher, J. P. Jasinski, J. M. Jasinsld, Polyhedron, 1997, 16, 2749.
[4] M. A. Ali, M. H. Kadir, M. Nazimuddin, S. M. M. H. Majumder, M. T .H. Tarafder, M. A. Khair, Ind. J. Chem, 1988, 27A, 1064.
[5] M. A. Ali, S. E. Livingstone, Coord. Chem. Rev., 1974, 13, 101.
[6] Y.-P. Tian, C.-Y. Duan, Z.-L. LU, X.-Z. You, Polyhedron, 1996, 15, 2263.
[7] M. A. Ali, K. K. Dey, M. Nazimuddin, F. E. Smith, R. J. Butcher, J. P. Jasinski, J. M. Jasinski, Polyhedron, 1996, 5, 3331.
[8] M. A. Ali, M. Nazimuddin, R. Shaha, R. J. Butcher, J. C. Bryan, Polyhedron, 1998, 17, 3955.
[9] N. Bharti, M. R. Maurya, F. Naqvia and A. Azama, Bioorg. Med. Chem. Lett. 2000, 10, 2243-2245
[10] S. Bhattacharjee, R. Bhattacharyya, J. Chem. Soc., Dalton Trans., 1992, 1357.
[11] B. Neelama, M. R. Maurya, N. Fehmidaa, B. Alokc, B. Sudhad, A. Amira, Eur. J. Med. Chem. 2000, 35, 481-486
[12] C. Y. Duan, Y. P. Tian, X. Z. You, T. C. W. Mak, Polyhedron, 16, 1997, 4097.
[13] S. M. M. H. Majumder, M. A. Ali, F. E. Smith, M. A. U. Mridha, Polyhedron, 1995, 7, 2153.
[14] M. E. Hossain, M. N. Alam, M. A. Ali, M. Nazimuddin, F. E. Smith, R. C. Hynes, Polyhedron, 1996, 15, 973.
[15] Y.-P. Tian, C.-Y. Duan, Z.-L. Lu and X.-Z. You, Polyhedron 1996, 15, 2263-2271.
[16] M. A.r Ali, A. H. Mirza, M.i H. S.A. Hamid,. V. Bernhardt, Polyhedron, 2005, 24, 383-390
[17] B. S. A. Thahira Ravoof, A. Karen, M. Crouse, I. M. Tahir, A. R. Cowley, M. A. Alic, Polyhedron, 2007, 26, 1159-1165
[18] Z.-M. Zhong, X.-J., R. Xing, S. Liu, Z.-Y. Guo, X.-L Chena, and P. Lia, Bioorg. Med. Chem., 2007, 15, 3775-3782
[19] M. A. Ali, A. H. Mirza, M. H. S. A. Hamid, F. H. Bujang, P. V. Bernhardt, Polyhedron, 2004, 23 2405-2412.
[20] M. A. Ali, A. H. Mirza, R. J. Butcher, M. T. H. Tarafder, M.. Ali, Inorg. Chim. Acta, 2001, 320, 1-6.
[21] M. B. Ferrari, S. Capacchi, G. Pelosi, G. Reffo, P. Tarasconi, R. Albertini, S. Pinelli, P. Lunghi, Inorg. Chim. Acta, 1999, 286, 134.
[22] D. L. Klaymen, J. P. Scovill, J. Bruce, J. F. Bartosevich, J. Med. Chem., 1984, 27, 87.
[23] R. Yuan, Y.-Q. Song, Y.-Q. Chai, S.-X. Xia, Q.-Y. Zhong, B. Yi, M. Ying, G.-L. Shen, R.-Q. Yu, Talanta, 1999, 48, 649-657
[24] G. M. de Lima, J. L. Nero, H. Beraldo, H. G. L. Siebald, D. J. Duncalf, J. Mol. Struct. 2002, 604, 287
[25] X.-X. Lu, S.-Y. Qin, Z.-Y. Zhou, V. W.-W. Yama, Inorg. Chim. Acta, 2003, 346 49-56
[26] R. A. Sanchez-Delgado, K. Lazardi, L. Rincort, J. A. Urbina, J. Med. Chem., 1993, 36, 2041.
[27] G. M. de Lima, J. L. Neto, H. Beraldo, H. G. L. Siebald, D. J. Duncalf, J. Mol. Struct., 2002, 604, 287.
[28] L. Mishra, J. Indian Chem. Soc., 1999, 76,175.
[29] M. A. Ali, C. M. Haroon, M. Nazimuddin, S. M. M. H. Majumder, M. T. H. Tarafder, M.A. Khair, Transition Met. Chem., 1992, 17, 133.
[30] M. A. Ali, N. E. Ibrahim, R. J. Butcher, J. P. Jasinski, J. M. Jasinski, J. C. Bryan, Polyhedron, 1998, 17, 1803.
[31] M. A. Ali, S. M. G. Hossain, S. M. M. H. Majumder, M. Nazimuddin, M. T. H. Tarafder, Polyhedron, 1987, 6,1653.
[32] M. A. Ali, R. N. Bose, J. Inorg. Nucl. Chem., 1977, 39, 265.
[33] M. A. Ali, R. N. Bose, Polyhedron, 1984, 3,517.
[34] M. T. H. Tarafder, Teng-Jin Khoo, Karen A. Crouse, A.M. Ali, B. M. Yamin, H.-K. Fun, Polyhedron, 2002, 21, 2691.
[35] M. Albota, D, Belionne, et al., Science, 1998, 281, 1653.
[36] T. Kogej, J. W. Perry,et al., Chem. Phys. Let., 1998, 298, 1.
[37] 周爱民等，安徽大学学报(自然科学版)，2002，26，76．
[38] J. W. Perry, S. R. Marder, et al., Nonlinear Optics, 1999, 21,225.
[39] S. R. Marder and S. R. Perry, [M]. New York: McGraw-Hill 2000 Yearbook Science and Technology, 2000.
[40] B. N. Cumpston, S. Ananthayel, et al., Nature, 1999, 389, 51.
[41] B. H. Cumpston, S. P. Ananthavel, et al. Nature, 1999, 398, 51.
[42] B. A. Reinhardt, L. L. Brott, et al., Chem. Mater, 1998, 10, 1863.
[43] 郁建华，田玉鹏，施鹏飞，安徽大学学报(自然科学版)，2003，27，85．
[44] K. J. Moon, H. K. Shim, et al., Macromol., 1996, 29, 681.
[45] D. M. Burland, R. D. Miller, C.-A.Walsh, Chem. Rev., 1994, 94, 31.
[46] C.-F. Zhao, C.K. Park, P.N. Prasad, et al., Chem. Mater, 1995, 7, 1237.
[47] Y.-P. Tian, C.-Y. Duan, X.-Z You, Transit. Met. Chem., 1998, 23, 17
[1] S. Handa, V. Gnanadesikan, S. Matsunaga, M. J. Shibasaki, Am. Chem. Soc., 2007;129(16); 4900-4901.
[2] N. Nimitsifiwat, E. L.Marshall, V. C. Gibson, M. R. J. Elsegood, S. H. Dale, J. Am. Chem.Soc., 2004, 126(42), 13598-13599.
[3] J. A. Riddle, S. P. Lathrop, J. C. Bollinger, D. J. Lee, Am. Chem. Soc., 2006; 128(34),10986-10987.
[4] M. Zhao, C. Zhong, C. Stern, A. G. M. Barrett, B. M. Hoffman, J. Am. Chem. Soc., 2005;127(27), 9769-9775.
[5] D. W. Roberts, A. O. Aptula, G. Patlewicz, Chem. Res. Toxicol., 2006; 19(9), 1228-1233.
[6] T. Tanaka, Y. Yasuda, M. Hayashi, J. Org. Chem., 2006, 71(18), 7091-7093.
[7] Z. Tang, X. Chen, X. Pang, Y. Yang, X. Zhang, X.Jing, Biomacromol., 2004; 5(3); 965-970.
[8] 王维群 营养学北京：高等教育出版社，2001．
[9] 赵霖，中华医学杂志，1995，75，2302．
[10] 吴嘉惠，任榕娜，营养学报，1995，17，3633．
[11] 李云，王瑞淑，营养学报，1997，19，1964．
[12] 余章机，黄时宪，西南农业学报，1997，10，815．
[13] 吴嘉惠，吴永冰，营养学报，1994，16，446．
[14] 李正及银，赵法，营养学报，1997，19，388．
[15] 吴嘉惠，徐迪雄，营养学报，1997，19，398．
[16] 徐迪雄，白家驷，第三军医大学学报，1997，19，4549．
[17] 李积胜，徐鹏霄，营养学报，1998，20，211．
[18] 孔祥英，卞修武，第三军医大学学报，1996，18，3401．
[19] 李积胜，徐鹏霄，营养学报，1997，19，3961．
[20] 盛晓阳，洪昭毅，营养学报，1994，16，115．
[21] 文建国，李玉绿，湖南医科大学学报，1996，21，2951．
[22] 罗子国，李维信，解剖学报，1999，30，861．
[23] 周藻初，许立庆，哈尔滨医科大学学报，1996，30，11．
[25] 徐艳钢，汤雪琴，中国公共卫生学报,1993，12，298
[26] 邵英，方锦，临床眼科杂志，1998，6，277。
[27] 马国东，冰雪运动，2005，4，85．
[31] X.-Y. Qiu, Ata Cryst., E62, 2006, m717.
[32] L. Tatar, D.Ulku and O. Atakol, Acta Cryst. C55, 1999, 508.
[33] Y. Chen, Acta Cryst. E62, 2006, m204..
[1] A. Escuer, G. Aromi, Eur. J. Inorg. Chem., 2006, 4721.
[35] C. Koch, A. Malassa, C. Agthe, H. Gorls, R. Biedermann, H. Krautscheid, M.Westerhausen, Z. Anorg. Allg. Chem., 2007, 633,375.
[36] A. Roth, A. Buchholz, W. Plass, Z. Anorg. Allg. Chem., 2007, 633, 383.
[37] W. R. Knapp, J. G. Thomas, D. P. Martin, M. A. Braverman, R. J. Troviteh, R. L.LaDuca, Z. Anorg. Allg. Chem., 2007, 633, 575.
[38] M. Kloskowski, D. Pursche, R.-D. Hoffmann, R. Pottgen, M. Lage, A.Hammerschmidt,T. Glaser, B. Krebs, Z. Anorg. Allg. Chem., 2007, 633, 106.
[39] F. Marandi, B. Mirtamizdoust, A. A. Soudi, V. T. Yilmaz, C. Kazak, Z. Anorg. Allg.Chem., 2006, 632, 2380.
[40] S. Sarkar, A. Mondal, M. S. El Fallah, J. Ribas, D. Chopra, H. Stoeckli-Evans, K. K.Rajak, Polyhedron, 2006, 25, 25.
[41] M. Zbiri, S. Saha, C. Adhikary, S. Chaudhuri, C. Daul, S. Koner, Inorg. Chim. Acta,2006, 359, 1193.
[42] Z.-L. You, H.-L. Zhu, Z. Anorg. Allg. Chem., 2004, 630, 2754.
[43] Z.-L. You, H.-L. Zhu, Z. Anorg. Allg. Chem., 2006, 632, 140.
[44] I. Romero, L. Dubois, M.-N. Collomb, A. Deronzier, J.-M. Latour, J. Pecaut, Inorg.Chem. 2002, 41, 1795.
[45] J. Ribas, A. Escuer, M. Montfort, R. Vicente, R. Cortes, L. Lezama, T. Rojo, Coord.Chem. Rev. 1999, 193-195, 1027.
[46] J. Tercero, C. Diaz, J. Ribas, E. Ruiz, J. Mahia, M. Maestro, Inorg. Chem., 2002, 41,6780.
[47] Y.-X. Sun, Z.-L. You, Z. Anorg. Allg. Chem., 2006, 632, 1566.
[48] Z.-L. You, Z. Anorg. Allg. Chem., 2006, 632, 664-668.
[49] Y. Ma, W. Zhang, G.-F. Xu, K. Yoshimura, D.-Z. Liao, Z.-H. Jiang, S.-P. Yan, Z. Anorg.Allg. Chem,. 2007, 633, 657-660.
[50] L.-N. Zhu, N. Xu, Y. Yang, D.-Z. Liao, Z.-H. Jiang, S.-P. Yan, P. Cheng, Z. Anorg. Allg.Chem., 2006, 632, 2500-2504.
[51] M. Nayak, R. Koner, H.-H. Lin, U. Florke, H.-H. Wei, S. Mohanta, Inorg. Chem., 2006,45, 10764.
[52] S. Dhar, D. Senapati, P. K. Das, P. Chattopadhyay, M. Nethaji, A. R. Chakravarty, J.Am. Chem. Soc. 2003, 125, 12118.
[1] J. F. Stevens, A. W. Taylor, G. B. Nickerson, M. Ivancic, J. Henning, A. Haunold, M. L.Deinzer, Phytochemistry, 2000, 53, 759.
[2] S. Shibata, Anti-tumorigenic chalcone. Stem. Cell., 1994,12, 44.
[3] M. A. Devi, N.P. Das, Cancer Lett., 1993, 69, 191..
[4] K. Zhang, N.P.Das, Biochem. Pharmacol, 1994, 47, 2063.
[5] M. L Edwards, D.M. Stemerick. P. S. Sunkara, et al., J. Med. Chem., 1990, 33, 1948.
[6] H. Kagechika, E. Kawachi, Y. Hashimoto, et al. J. Med. Chem, 1989, 32, 834.
[7] B. Liasset, C. Doucern, J.C. Dore, et al. Biochem. Pharmacol, 1993, 46, 1257.
[8] Y. Inamori, K. Baba, H. Tsujibo, et al., Chem. Pharm. Bull, 1991, 39, 1604.
[9] R. Edenharder, I. Petersdorff, R. Rauscher, et al. Mutation Res., 1993, 287, 261.
[10] R. J. Miksicek, Mol. Pharmacol, 1993, 44, 37.
[11] (a) S. F. Nielsen, S. B. Christensen, G. Cruciani, A. Kharazmi, T. Liljefors, J. Med.Chem., 1998, 41, 4819; (b) R. Li, G. L. Kenyon, F. E. Cohen, X. Chen, B. Gong, J. N. Dominguez, E. Davidson, G. Kurzban, R. E. Miller, E. O. Nuzum, P. J. Rosenthal, J. H.Mckerrow, J. Meal. Chem., 1995, 38, 5031; (c) M. Liu, P. Wilairat, M. L. Go, J. Med. Chem., 2001, 44, 4443.
[12] J. Rojas, M. Paya, J. N. Dominguez, M. L. Ferranidz, Bioorg. Med. Chem. Lett., 2002, 12, 1951.
[13] (a) H. K. Hsieh, e T. H. Le, J. P. Wang, J. J. Wang, C. N. Lin, Pharm. Res., 1998, 15, 39;(b) M. A. Babu, N. Shakya, P. Prathipati, S. G. Kaskhedikar, A. K. Saxena, Bioorg. Med.Chem., 2003, 10, 4035.
[14] (a) S. K. Kumar, E. Hager, C. Pettit, H. Gurulingappa, N. E. Davidson, S. R. Khan, J.Med. Chem., 2003, 46, 2813; (b) S. Ducki, R. Forrest, J. A. Hadfield, A. Kendall, N. J.Lawrence, A. T. McGown, D. Rennison, Bioorg. Med. Chem. Lett., 1998, 8, 1051.
[15] T. P. Frandesn, B. Svensson, Plant Mol. Biol., 1998, 37,1.
[16] M. Artico, R. D. Santo, R. Costi, E. Novellino, G. Greco, S. Massa, E. Tramontane M. E. Marongiu, A. D. Montis, P. L. Colla, J. Med. Chem. 1998,41,3984.
[17] F. Herencia, M. L Ferrandiz, Ubeda A., J. N. Domynguez, J. E .Charris, G. M. Lobo, and A M. J.lcaraz, Med. Chem. Lett., 1998, 8,1169.
[18] X. Chen, C. Plasencia, Y. Hou, N. Neamati, J. Med. Chem., 2005,48,1098.
[19] E.M. Kosower, T. Miyadera, J. Med. Chem., 1972,15, 307
[20] J. F. Stevens, A. W. Taylor, G. B. Nickerson, M. Ivancic, J. Henning, A. Haunold, M. L. Deinzer, Phytochemistry, 2000, 53, 759.
[21] S. F. Nielsen, S. B. Christensen, G. Cruciani, A. Kharazmi, T. Liljefors, J. Med. Chem., 1998,41,4819;
[22] R. Li, G. L. Kenyon, F. E. Cohen, X. Chen, B. Gong, J. N. Dominguez, E. Davidson, G. Kurzban, R. E. Miller, E. O. Nuzum, P. J. Rosenthal, J. H. Mckerrow, J. Med. Chem., 1995, 38,5031.
[23] M. Liu, P. Wilairat, M. L. Go, J. Med. Chem, 2001,44,4443.
[24] J. Rojas, M. Paya, J. N. Dominguez, M. L. Ferranidz, Bioorg. Med. Chem. Lett, 2002, 12,1951.
[25] S. K. Kumar, E. Hager, C. Pettit, H. Gurulingappa, N. E. Davidson, S. R. Khan, J. Med. Chem, 2003,46,2813.
[26]S. Ducki, R. Forrest, J. A. Hadfield, A. Kendall, N. J. Lawrence, A. T. McGown, D. Rennison, Bioorg. Med. Chem. Lett, 1998, 8,1051.
[27] D. N. Dhar, J. B. Lal, J. Org. Chem. 1958, 23, 1159; S.Wattanasin, W.S. Murphy, Synthesis 1980, 8, 647.
[28] R. E. Lyle, L. P. Paradis, J. Am. Chem. Soc, 1955, 77,6667.
[29] H.K.Hsieh, T. H.Lee, J. P. Wang, J. J. Wang, C. N. Lin, Pharm. Res, 1998,15,39.
[30] M. A. Babu, N. Shakya, P. Prathipati, S. G. Kaskhedikar, A. K. Saxena, Bioorg. Med. Chem, 2003,10,4035.
[31] S. K. Kumar, E. Hager, C. Pettit, H. Gurulingappa, N. E. Davidson, S. R. Khan, J. Med. Chem, 1998,41,4161.
[32] N. H. Nam, Y. K, Y. J. You, D. H. Hong, H. M. Kim, B. Z. Ahn, Eur. J. Med. Chem, 2003,38,179.
[33] T. P. Frandesn, B. Svensson, Plant Mol. Biol, 1998, 37,1.
[34] M. Artico, R. D. Santo, R. Costi, E. Novellino, G. Greco, S. Massa, E. Tramontano, M. E. Marongiu, A. D. Montis, P. L. Colla, J. Med. Chem, 1998,41, 3984.
[2] S. Handa, V. Gnanadesikan, S.Matsunaga, M.Shibasaki, J. Am. Chem. Soc., 2007, 129, 4900-4901.
[3] C. Chen, L. Hong, Z.-Q.Xu, L.Liu, R.Wang, Org. Lett., 2006, 8, 2277-2280.
[4] G. Occhipinti, V. R. Jensen, H. R. Bjorsvik, J. Org. Chem., 2007, 72, 3561-3564.
[5] X.-P.Yang, Jones R. A., M. M.Oye, A. L Holmes, W.-K.Wong, Cryst. Growth Des., 2006, 6, 2122-2125.
[6] J. A. Riddle, S. P. Lathrop, J. C. Bollinger, D. Lee, J. Am. Chem. Soc. 2006; 128(34); 10986-10987.
[7] R. Jarvo Elizabeth, M. L. Brian, N. J. Eric., Angew. Chem. Int. Edi., 2005, 44, 6043-6046.
[8] M. Kazuhiro, Y.Sawada, S. Bunnai, S.Ken, K.Tsutomu, Angew. Chem. Int. Edi., 2005, 44, 4935-4939.
[9] O. Akihiro, S. Tomoyuki, T.Ohshima, H.Masu, Y.Kentaro, S.Masakatsu, Angew. Chem. 2005, 117, 4640-4643.
[10] J. L. Sessler, E. Tomat, V. M. Lynch, J. Am. Chem. Soc. 2006; 128(34); 10986-10987.
[11] T. Tanaka, Y. Yasuda, M. Hayashi, J. Org. Chem., 2006, 71, 7091-7093.
[12] 游效曾，孟庆金，韩万书主编 配位化学进展．-北京：高等教育出版社，2000．
[13] M. Eddaoudi, D. B Moler., H.L.Chen, T.M.Reineke, M. Okeeffe, O.M.Yaghi, Acc. Chem. Res., 2001, 34, 319.
[14] S.-S. Chui., S.M.F.Lo, J.P.H.Charmant, A.G.Orpen, I.D.Williams, Sci., 1999, 283, 1148.
[15] 林君，庞茂林，韩银花，于敏，张洪杰，无机化学学报，2001，17，153．
[16] Q. -G. Meng, H.-J.Zhang, S.-B.Wang, L.-S.Fu, Y.-X.Yang, Mater. Lett., 2000, 45,213.
[17] 林君，苏锵，稀土，1994，15，42．
[18] T. Jin, S.Tsutsumi, Y. Deguchi, K. Machid, J. Electrochem. Soc., 1995, 142, L195.
[19]. G.. Qian, M.-J. Wang, J. Phys. Chem. Solid, 1997, 58, 375.
[20] 王金龙，武汉大学硕士学位论文，2003．
[21] 袁良杰，武汉大学博士学位论文，2003．
[22] K. Dey, J. Scient. Ind. Res. India, 1974, 33, 76.
[23] F. P. Dwyer, D. P. Mellor, Chelating Agents and Metal Chelates. New York: Academic Press Inc, 1964.
[24] J. W. Smith. In: Patai S. The Chemstry of Carbon-Nitrogen Double Bond. London: Interscience Publisher Ltd, 1970, Chapter 5.
[25] H. Malcolm, C. C. Judith, Gallucci, and H.-S. Zhen, Inorg. Chem., 2001, 40, 5051.
[26] A. K. Patra, M. M. Olmstead and P. K. Mascharak, Inorg. Chem., 2002, 41, 5403;
[27] C. Olivier, C. Francoise, D. Andrea, S. Claudio, V. S. Joris, and G. F. V. Maria, Inorg. Chem., 2003, 42, 6432.
[28] J. P. Cean, F. L Jean., L. Christine, G. L. Pascal, and D. Francoise and N. Keitaro, Inorg. Chem. 2005, 44, 1973.
[29] D. Renata, A. Bart, L. Nele, D. Ileana, D. Valerian, V. Francis, J Coord. Chem. Rev., 2005, 249, 3055.
[30] M. R. Jose., R. Horacio, C. Armando, and S. P. G. L Rosa., and L. K. N. Christine, F. Norberto, Chem. Mater., 2006, 18, 1174.
[31] K. Sah Ajay, T. Tomoaki, and M. Masahiro, Inorg. Chem., 2006, 45, 2083.
[32] M. B. Virginie, Saeed I. K., and Mahdi M. A., Inorg. Chem., 2001, 40, 6767.
[33] P. Reinhard, L. Stefan, T. Carsten, A. O.Michael and S. Ekkehard, Inorg. Chem., 2003, 42, 8231.
[34] G. Park, F. Lu H., N. Ye, M. W. Brechbiel, S. V. Torti, F. M. Torti, and R. P. Planalp, JBIC 1998, 3,449.
[35] V. Paola, I. Matteo, A. D. Irini, L. C. Paolo, B. Bernadetta, L. Roberta, Eur. J. Med. Chem., 2006, 41, 624.
[36] F.-Y. Chen, W.-K. Cao, S.-Y. He, B.-H. Wang, Y.-M. Zhang, Acta Phys. -China. Sin., 2006, 22(3), 280-285.
[37] D. L. Alessandro, O. Valentina, S. Barbara, C. Cenzo, L. S. Maria and T. C. Maria, J. Antimicrob. Chemoth., 2002, 49, 275.
[38] T. C. Maria, C. Cenzo, O. Valentina, C. P. Maria, Maria L. Schivo, D. L. Alessandro, Eur. J. Med. Chem., 1999, 34, 1071.
[39] M. Patricia, L. Virginie, S. Christian, and G. Philippe, Bioorg. Med. Chem. Let., 2006, 16, 31.
[40] T. B. Chaston, D. R. Richardson, J Biol Inorg Chem, 2003, 8, 427.
[41] B. B. Safoklov, E. G. Atovmyan, L. A. Nikonova, V. V. Tkachev, and S. M. Aldoshin, Russ. Chem. B., 2002, 51, 2224.
[42] R. Maccari, R. Ottanaa and M. G. Vigorita, Bioorg. Med. Chem. Let., 2005, 15, 2509.
[43] D. Sriram, P. Yogeeswari and K. Madhu, Bioorg. Med. Chem. Let., 2005, 15, 4502.
[44] D. Sriram, P. Yogeeswari and K. Madhu, Bioorg. Med. Chem. Let., 2006, 16, 876.
[45] P. S. J. Floriano, E .Javier, L. F. Marcelled., P. M. Yvonne, V. N. d. S. Marcus, R. A. V. Thatyana, L. W. James, M. S. V. W. Solange, J. Mol. Struct., 2006, 788, 63.
[46] D. G. Rando, A. C. Doriguetto, J. Ellena, S. D. N. Leite, E. A. Varanda, E. I. Ferreira, Eur. J. Med. Chem., 2006, 41, 1196.
[47] D. D. Yu and B. M. Forman, Bioorg. & Med. Chem. Let., 2005, 15, 1311.
[48] S. Sivaramaiah and R. P. Raveendra, J. Anal. Chem., 2005, 60, 828.
[49] S. Guniz Kuc, ukuCguzel, A. Mazi, F. Sahin, S. Ozturk, J. Stables, Eur. J. Med. Chem., 2003, 38, 1005.
[50] B. -D. Wang, Z. -Y. Yang and T.-R. Li, Bioorg. Med. Chem. Let. 2006, 14, 6012.
[51] C. Xu, H. Y. Mao, H. Y. Zhang, H. L. Liu, J. Mol. Struct., 2003, 658, 59.
[52] W. Xiao, Z. I. Lu, X. J. Wang, C. Y. Su, K. B. Yu, H. Q. Liu, B. S. Kang, Polyhedron, 2000, 19, 1295.
[53] C. Pelizzi, G. Pelizzi, and P. Tatasconi, J. Chem. Soc. Dalton Trans., 1985, 215
[54] C. Lorenzini, C. Pelizzi, G. Pelizzi, and G. Pelizzi, J. Chem. Soc. Dalton Trans., 1983, 721.
[55] Z. H. Liu, C. Y. Duan, J. Hu and X. Z. You, Inorg. Chem., 1999, 38, 1719
[56] 陈小华刘世雄，无机化学学报，2005，21，15．
[57] 胡宗球，吴宇，加兵，施少敏，祝心德，宋发辉，无机化学学报，2005，21，1715．
[58] 孙纲春，曲建强，王流芳，陈耐生，李燕，陈晓光，谢晶曦，无机化学学报，2005，21，1069．
[59] 杨健国，潘富友，李钧敏，无机化学学报，2005，21，1593．
[60] 肖子敬，刘世雄，林墀昌，无机化学学报，2004，20，513．
[61] F. Y. Chen. W. K Cao, S. Y. He, B. H. Wang, Y. M. Zhang, Acta Phys. -Chim. Sin., 2006, 22, 280.
[62] N. R. Sumita, D. D. Mishra, R. C.Maurya and R. N. Nageswara., Polyhedron, 1997, 16, 1825.
[63] S.-Y. He, R. Yang, W.-T. Wu, Q.-Z. Shi, D.-Q. Wang and D.-R. An, Chin. J. Chem., 2005, 23, 1198.
[64] T. Shi, S.Y. He, X. F. Wang, Y.B. Wang, Z.X. Tang and Z.Y. Wen, J. Mol. Struet., 2005, 732, 201.
[65] S. Naskar, S. Biswas, D. Mishra, B. Adhikary, L.R. Falvello, T. Soler, C.H. Schwalbe and S.K. Chattopadhyay, Inorg. Chim.Acta, 2004, 357,4257.
[66] N. K. Singh, Nagendra Singh, G. C. Prasad, h A. Sodhi and Anju Shrivastava, Bioorg. Med. Chrm., 1997, 5,245.
[67] R. M. R. Ottana, B. Bottari, E. Rotondo and M. G. Vigorita, Bioorg. Med. Chem. Let., 2004,14,5731.
[68] B. Bottari, R. Maccari, F. Monforte, R. OttanaA, E. Rotondo and M. G. Vigoritaa, Bioorg. Med. Chem. Let., 2001,11,301.
[69] P. K. Singh, D. N. Kumar, Spectrochimica Acta Part A, 2006,64, 853.
[70] B. Bottari, R. Maccari, F. Monforte, R. OttanaA, E. Rotondo and M. G. Vigorita, Bioorg. Med. Chem. Let., 2000,10,657.
[71] D. R. Richardson and Paul V. Bernhardt, JBIC, 1999,4,266.
[72] F. Cariati, U. Caruso, R. Centore, W. Marcolli, A. De Maria, Panunzi, A. Roviello, and A.Tuzi, Inorg, Chem, 2002,41,6597.
[73] D.B. Wang, B.H.Chen, Y.X. Ma, Syn. React. Inorg. Met-Org. Chem.,1997,27,479.
[74] M. Mohan, M. P. Gupta and L. Chandra, J Chem. Acta, 1988,151,61.
[75] Z. H..Chohan, A.Rauf, Syn. React. Inorg. Met-Org. Chem, 1996,26,591.
[76] M.Kondo, K.Nabari, T. Horiba,, Y. Me,, M. K. Kabir, R. P. Sarker, E. Shimizu, Y. Shimizu,.F.W. Yang, Inorg. Chem. Commun, 2003,6,154.
[77] F. Averseng, P. G. Lacroix, I. Malfant, N. Perisse, and C. L.K. Nakatani, Inorg. Chem, 2001,40,3797.
[78] Z.-L. Lu, M. Yuan, F. Pan, S. Gao, D.-Q. Zhang, and D.-B. Zhu, Inorg. Chem, 2006,45, 3538.
[79] C. A. Bear, J. M. Waters, T. N. Waters, J. Chem. Soc, Dalton Trans, 1974,1059.
[80] (a) Reddy et al. Inorg. Chem, 1998,37,5978; (b) Li et al. Inorg. Chem. Acta, 1998, 271,99.
[81] (a) Christian D. Be'rube', Sandro Gambarotta, and Glenn P. A. Yap, Organometallics, 2003,22,434. (b) T.-F. Jiao and M.-H. Liu, J. Phys. Chem. B, 2005,109,2532. (c) D. Agustin, G. Rima, H. Gornitzka, and J. Barrau, Organometallics, 2000,19,4276. (d)D. Agustin, G. Rima, H. Gornitzka and J. Barrau, Inorg. Chem, 2000, 39, 5492.(e) T.-W. Wong, T.-C. Lau and W.-T. Wong, Inorg. Chem, 1999,38,6181. (f) J. M. McInnes, D. Swallow, A. J. Blake, and P. Mountford, Inorg. Chem, 1998,37,5970. (g) J. M. Rivera, H. Reyes, A. Cortes, and R. Santillan, Chem. Mater, 2006,18,1174.(h) F. Averseng, C. Lepetit, P.I G. Lacroix, and J. P. Tuchagues, Chem. Mater, 2000,12,2225. (g) P. G. Lacroix, S. D. Bella, I. Ledoux, Chem. Mater., 1996, 8, 541. (h) E. Gallo, E. Solari, N. Re, Carlo Floriani, C.-V. Angiola and C. Rizzoli J. Am. Chem. Soc., 1997, 119, 5144.
[82] N. K. Dutt, K.Nag, J. Inorg. Nucl. Chem., 1968, 30, 2493.
[83] R. L. Dutta, B. R. Das, J. Scient. Ind. Res., 1988, 47, 547.
[84] T. Kido, Y. Ikuta, Y. Sunatsuki, Y. Ogawa, N. Re N. Matsumoto, Inorg. Chem., 2003, 42, 398.
[85] Z.-L. You, W.-S. Liu, H.-L. Zhu and H.-K. Fun, Trans.Met.Chem., 2005, 30, 1.
[86] Z.-L. You, H.-L. Zhu, and W.-S. Liu, Trans. Met. Chem., 2004, 29, 653.
[87] Z.-L. You, and H.-L. Zhu, Zinc. Z. Anorg. Allg. Chem., 2004, 630, 2754.
[88] Z.-L. You, H.-L. Zhu, and W.-S. Liu, Z. Anorg. Allg. Chem., 2004, 630, 1617.
[89] Y. Qu, H.-L. Zhu, Z.-L. You and M.-Y. Tan, Molecules, 2004, 9, 949.
[90] F. Averseng, P. G. Lacroix, I. Malfant, N. Perisse, and C. L. K. Nakatani, Inorg. Chem., 2001, 40, 3797.
[91] 黄春辉著．稀土配位化学．北京：科学出版社，1997．
[92] J. Lange, H. Elias, and H. P.J(?)rg Müller and U. Weser, Inorg. Chem., 2000, 39, 3342.
[93] S. G. Telfer, T. Sato, T. Harada, R. Kuroda, J. Lefebvre and D. B. Leznoff, Inorg. Chem., 2004, 43, 6168.
[94] Y.-B. Dong, L. Wang, J.-P. Ma, X.-X. Zhao, D.-Z. Shen and R.-Q. Huang, Crystal Growth & Design, 2006, 0, 1.
[95] Y.-B. Dong, M. D. Smith, H.-C. zur Loye, Inorg. Chem., 2000, 39, 4927.
[96] Y.-B. Dong, M. D. Smith, R. C. Layland, H.-C. zur Loye, Chem. Mater., 2000, 12, 1156.
[97] Y.-B. Dong, X. Zhao, B. Tang, H.-Y. Wang, R.-Q. Huang, M. D. Smith, H.-C. zur Loye, Chem. Commun., 2004, 2, 220.
[98] Y.-B. Dong, P. Wang, R.-Q. Huang, M. D. Smith, Inorg. Chem., 2004, 43, 4727.
[99] Y.-B.Dong, H.-Q. Zhang, J.-P. Ma, R.-Q. Huang, Cryst.Growth Des., 2005, 5, 1857.
[100] K. Ueno, A E. Martell, J. Phys. Chem.,1957, 61,257
[101] (a) N. K. Dutt, Inorg. Chem.,1968, 30, 2779; (b) N. K. Dutt, Inorg. Chem., 1968, 30, 3273.
[102] S. A. Schuetz, C.M. Silvernail, C. D. Incarvito, A. L. Rheingold, J. L. Clark, V. W. Day, and J. A. Belot, Inorg. Chem., 2004, 43, 6203.
[103] Paul D. Benny, Jenny L. Green, Hendrik P. Engelbrecht, Charles L. Barnes and Silvia S. Jurisson, Inorg. Chem., 2005, 44, 2381.
[104] S. A. Schuetz, V. W. Day, R. D. Sommer, A. L. Rheingold and J. A. Belot, Inorg. Chem., 2004, 40, 5292.
[105] 姚克敏，吴大庆，杨卫红，应用化学，1992，9，8．
[106] 杜向东，俞贤达，高等学校化学学报，1997，18，567．
[107] T. S. Reger, K. D. J. Janda, Am. Chem. Soc., 2000, 122, 6929.
[108] G.-J. Kim, S.-H. Kim, Catal. Lett., 1999, 57, 139.
[109] R C. Elder, Aust. J Chem., 1978, 31, 35.
[110] 陈红卫，朱志昂，张智慧等，无机化学学报，1996，12，178．
[111] (a)L. Thunus, R. Lejeune, Coord. Chem. Rev., 1999, 184, 125; (b) K. Wang, R. Li, Y. Cheng, B. Zhu, Coord. Chem. Rev., 1999, 190, 297; (c) J.-C.G. Bünzli, C. Piguet, Chem. Rev., 2002, 102, 1897; (d) H. Tsukube, S. Shinoda, Chem. Rev., 2002, 102, 2389;
[112] W. R. Paryzek, V. Patroniak, J. Lisowski, Coord. Chem. Rev., 1999, 185,451.
[113] V. Comblin, D. Gilsoul, M. Hermann, V. Humblet, V. Jacques, M.Mesbahi, C. Sauvage, J.F. Desreux, Coord. Chem. Rev., 1999, 185,451.
[114] B. Dietrich, P.Viout, J.-M. Lehn, Macrocyclic Chemistry, VCH Verlagsges ellschaft, Weinheim, 1993.
[115] J.-M. Lehn, Supramolecular Chemistry, VCH Verlagsgesellschaft, Weinheim, 1995.
[116] E.C.Constable, Metals and Ligand Reactivity, VCH Verlagsgesellschaft, Weinheim, 1996.
[117] J.R. Fredericks, A.D. Hamilton, in: A.D. Hamilton (Ed.),Supramolecular Control of Structure and Reactivity, Wiley, Chichester, 1996, Chapter 1.
[118] J.W.Steed, J.L.Atwood, Supramolecular Chemistry, Wiley, Chichester, 2000.
[119] J.P. Andre, E. Toth, H. Fischer, A. Seelig, H.R. Maicke, A.E. Merbach,Chem. Eur. J. 1999, 5, 2977.
[120] M. Woods, S. Aime, M. Botta, J.A.K. Howard, J.M. Moloney, M.Navet, D. Parker, M. Port, O. Rousseaux, J. Am. Chem. Soc., 2000,122, 9781.
[121] M. Botta, Eur. J. Inorg. Chem., 2000, 399.
[122] F.A. Dunand, R.S. Dickins, D. Parker, A. Merbach, Chem. Eur. J., 2001, 7, 5160.
[123] S. Aime, D.D.Castelli, F. Fedeli, E. Terreno, J. Am. Chem. Soc., 2002, 124, 9364.
[124] W. Li, G. Parigi, M. Fragai, C.Luchinat, T.J. Meade, Inorg. Chem., 2002, 41, 4018.
[125] M. Woods, Z. Kovacs, S.Zhang, A.D. Sherry, Angew. Chem. Int.Ed., 2003, 42, 5889.
[126] S. Zhang, R. Trokowski, A.D. Sherry, J. Am. Chem. Soc., 2003, 125, 15288.
[127] J.- C. G. Bünzli, C. Piguet, Chem. Rev., 2002, 102, 1897.
[128] N. Sabbatini, M. Guargigli, I. Manet, R. Ungaro, A. Casnati, R.Ziessel, G. Ulrich, Z. Asfari, J.-M. Lehn, Pure Appl. Chem., 1995, 67, 135.
[129] M.P. Oude Wolbers, F.C.J.M. van Veggel, B.H.M. Snellick-Ruel,J.W. Hofstraat, F.A.J. Guerts, D.N. Reinhoudt, J. Am. Chem. Soc, 1997,119,138.
[130] J. Huskens, J.A. Peters, H. Van Bekkum, Inorg. Chem., 1995, 34,1756.
[131] D. Parker, J.A.G. Williams, J. Chem. Soc, Dalton Trans., 1996, 3613.
[132]S. E.Matthews, C.W.Pouton, M.D.Threadgill, Adv. Drug Delivery Rev., 1996,18,219.
[133] D. Parker, Coord. Chem. Rev, 2000,205,109; Goddard III, J. Am. Chem. Soc, 1999, 121,6142.
[134] D. Parker, R.S. Dickins, H. Purschmann, C. Crossland, J.A.K.Howard, Chem. Rev, 2002,102,1977.
[135] Y. Bretonniere, M. Mazzanti, R. Wietzke, J. Pecaut, Chem. Commun, 2000,1543.
[136] J.-C.G. Bunzli, N. Andre, M. Elhabiri, G. Muller, C. Piguet, J.Alloys Compd, 2000,66, 303.
[137] C. Piguet, C. Edder, H. Nozary, F. Renaud, S. Rigault, J.-C.G.Bunzli, J. Alloys Compd, 2000,94,303.
[138] T.Gunnlaugsson, D.A.Mac D'onaill, D.Parker, J.Am.Chem. Soc, 2001,123,12866.
[139] C.M. Rudzinski, A.M. Young, D.G. Nocera, J. Am. Chem. Soc, 2002,124,1723.
[140] Y. Bretonni' ere, M.J. Cann, D. Parker, R. Slater, Chem. Commun, 2002,1930.
[141] P. Atkinson, Y. Bretonniere, D. Parker, Chem. Commun, 2004,438.
[142] D. Parker, Chem. Soc. Rev, 2004,33,156.
[143] E. Tdth, L. Helm, A.E. Merbach, in: J.A. McCleverty, T.J. Meyer(Eds.), Comprehensive Coordination Chemistry II, vol. 9, Elsevier, 2004, Chapter 19.
[144] (a) R.B. Lauffer, Chem. Rev, 1987, 87, 901; (b) P. Caravan, J.J. Ellison, T.J. McMurry, R.B. Lauffer, Chem. Rev, 1999, 99,2293.
[145] S. Zhang, K. Wu, A.D. Sherry, Angew. Chem. Int. Ed, 1999,38,3192.
[146] V. Comblin, D. Gilsoul, M. Hermann, V. Humblet, V. Jacques, M.Mesbahi, C. Sauvage, J.F. Desreux, Coord. Chem. Rev, 1999,451,185.
[147] J.P. Andre, E. Tdth, H. Fischer, A. Seelig, H.R. M¨acke, A.E. Merbach, Chem. Eur. J, 1999,5,2977.
[148] M. Woods, S. Aime, M. Botta, J.A.K. Howard, J.M. Moloney, M.Navet, D. Parker, M. Port, O. Rousseaux, J. Am. Chem. Soc, 2000,122, 9781.
[149] M. Botta, Eur. J. Inorg. Chem, 2000, 399.
[150] F.A. Dunand, R.S. Dickins, D. Parker, A. Merbach, Chem. Eur. J, 2001,7,5160.
[151] S.Aime, D.D.Castelli, F. Fedeli, E. Terreno, J. Am. Chem. Soc, 2002,124,9364.
[152] W. Li, G.Parigi, M.Fragai, C.Luchinat, T.J. Meade, Inorg. Chem, 2002,41,4018.
[153] M.Woods, Z. Kovacs, S. Zhang, A.D. Sherry, Angew. Chem. Int.Ed, 2003,42,5889.
[154] S. Zhang, R. Trokowski, A.D. Sherry, J. Am. Chem. Soc, 2003,125,15288.
[155] F. Yerly, A. Borel, L. Helm, A.E. Merbach, Chem. Eur. J, 2003,9, 5468.
[156] L.V. Elst, M. Port, I. Raynal, C. Simonot, R.N. Muller, Eur.J.Inorg. Chem., 2003, 2495.
[157] K. Kimpe, T.N. Parac-Vogt, S. Laurent, C. Pierart, L.V. Elst, R.N.Muller, K. Binnemans, Eur. J. Inorg. Chem., 2003, 3021.
[158] S. Jurisson, D. Berning, W. Jia, D. Ma, Chem. Rev., 1993, 93,1137.
[159] Y.H. Jang, M. Blanco, S. Dasgupta, D.A. Keire, J.E. Shively, W.A.Goddard III, J. Am. Chem. Soc, 1999,121,6142.
[160] H. Ali, J. E. Van Lier, Chem. Rev., 1999,99,2379.
[161] D.A. Keire, Y.H. Jang, L. Li, S. Dasgupta, W.A. Goddard III, J.E.Shively, Inorg. Chem., 2001,40,4310.
[162] J.L. Sessler, T.D. Mody, G.W. Hemmi, V. Lynch, S.W. Young, R.A.Miller, J. Am. Chem. Soc, 1993,115,10368.
[163] S.W.A. Bligh, N. Choi, C.F.G.C. Geraldes, S. Knoke, M. Mc-Partlin, M.J. Sanganee, T.M. Woodroffe, J. Chem. Soc, DaltonTrans., 1997,4119.
[164] L. Thunus, R. Lejeune, Coord. Chem. Rev. 1999,184,125.
[165] K. Wang, R. Li, Y. Cheng, B. Zhu, Coord. Chem. Rev., 1999,297,190.
[166] D. Kong, L. Meng, L. Song, Y. Xie, Transition Met. Chem., 1999,24,553.
[167] J.L. Sessler, R.A. Miller, Biochem. Pharmacol., 2000, 59, 733.
[168] L.A.D. Williams, R.C. Howell, R. Young, I.A. Kahwa, Comp.Biochem. Physiol. Part C: Toxicol. Pharmacol., 2001,128,119.
[169] M. Woods, Z. Kovacs, A.D. Sherry, J. Supramolecular Chem., 2002,2,1.
[170] R.W. Hay, N. Govan, J. Chem. Soc, Chem. Commun., 1990,714.
[171] J.R. Morrow, L.A. Buttery, V.M. Shelton, K.A. Berback, J. Am.Chem. Soc, 1992,114, 1903.
[172] N. Hayashi, N. Takeda, T. Shiiba, M. Yashiro, K. Watanabe, M.Komiyama, Inorg. Chem., 1993,32, 5889.
[173] J. K. Bashkin, L.A. Jenkins, Comments Inorg. Chem., 1994,16, 77.
[174] B. K. Takasaki, J. Chin, J. Am. Chem. Soc, 1994,116,1121.
[175] K. Matsumura, M. Endo, M. Komiyama, J. Chem. Soc, Chem. Commun., 1994,2019.
[176] D. Magda, R.A. Miller, J.L. Sessler, B.L. Iverson, J. Am. Chem.Soc, 1994,116,7439.
[177] K. G. Ragunathan, H.-J. Schneider, Angew. Chem. Int. Ed., 1996,35,1219.
[178] R. Haner, J. Hall, Antisense Nucl. Acid Drug Dev., 1997,7,423.
[179] B.F. Baker, H. Khalili, N. Wei, J.R. Morrow, J. Am. Chem. Soc, 1997,19, 8749.
[180] P.E. Jurek, A.E. Martell, Chem. Commun., 1999,1609.
[181] B.F. Baker, S.S. Lot, J. Kringel, S. Cheng-Flournoy, P. Villiet, H.M.Sasmor, A.M. Siwkowski, L.L. Chappell, J.R. Morrow, Nucl. Acids Res., 1999,27,1547.
[182] D.M. Epstein, L.L. Chappell, H. Khalili, R.M. Supkowski, W.DeW.Horrocks Jr., J.R. Morrow, Inorg. Chem., 2000, 39,2130.
[183] S.J. Franklin, Curr. Opin. Chem. Biol., 2001,5,201.
[184] S.W.A. Bligh, N. Choi, E.G. Evagorou, M. McPartlin, K.N. White,J. Chem. Soc, Dalton Trans., 2001, 3169.
[185] C. Liu, M. Wang, T. Zhang, H. Sun, Coord. Chem. Rev., 2004,248,147.
[186] C. H. Evans, in: E. Frieden (Ed.), Biochemistry of Lanthanides, Plenum Press, New York, 1990, Chapter 9.
[187] J.-C.G. B¨unzli, in: K.A. Gschneidner Jr., L. Eyring (Eds.), Handbookon the Physics and Chemistry of Rare Earths, vol. 9, Elsevier, Amsterdam, 1987, Chapter 60.
[188] M.F. Tweedle, in: J.-C.G. Bunzli, G.R. Choppin (Eds.), LanthanideProbes in Life, Chemical and Earth Sciences, Elsevier, Amsterdam, 1989, Chapter 5.
[189] H. Tsukube, S. Shinoda, Chem. Rev., 2002,102,2389.
[190] P.H. Brown, A.H. Rathjen, R.D. Graham, D.E. Tribe, in: K.A.Gschneidner Jr., L. Eyring (Eds.), Handbook on Physics and Chemistryof Rare Earths, vol. 13, Elsevier Science Publishers, Amsterdam,1990, Chapter 92.
[191] J.R. Duffield, D.M. Taylor, D.R. Williams, in: K.A. GschneidnerJr., L. Eyring, G.R. Choppin, G.H. Lander (Eds.), Handbook onPhysics and Chemistry of Rare Earths, vol. 18, Elsevier Science Publishers, Amsterdam, 1994, Chapter 129.
[192] J.M. Harrowfield, M.I. Ogden, R. Richmond, A.H. White, J. Chem.Soc, Dalton Trans., 1991,2153.
[193] W. Radecka-Paryzek, Inorg. Chim. Acta, 1979,35,349.
[194] W. Radecka-Paryzek, Inorg. Chim. Acta, 1979,34,5.
[195] W. Radecka-Paryzek, Inorg. Chim. Acta, 1981, 52 261.
[196] W. Radecka-Paryzek, Polyhedron, 1989, 8,1217.
[197] W. Radecka-Paryzek, E. Luks, Polyhedron, 1994, 13, 899.
[198] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, Pol. J. Chem., 1995, 69,1.
[199] J. Cai, J.G. Muller, C.J. Burrows, Supramol. Chem., 2002,14,121.
[200] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, Polyhedron, 1995,14,2059.
[201] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, Collect. Czech.Chem. Commun., 1998,63,363.
[202] W. Radecka-Paryzek, V. Patroniak-Krzyminiewska, H. Litkowska, Polyhedron, 1998, 17,1477.
[203] W. Radecka-Paryzek, H. Litkowska, J. Alloys Compd., 2000,435,300.
[204] W. Radecka-Paryzek, V. Patroniak, M. Kubicki, Polyhedron, 2003,22,2773.
[205] W.Radecka-Paryzek, V.Patroniak, M.Kubicki, Inorg. Chem. Commun., 2004, 7,455.
[206] V. Patroniak, M. Kubicki, A. Mondry, J. Lisowski, W. Radecka-Paryzek, Dalton Trans., 2004,3295.
[207] W. Radecka-Paryzek, Inorg. Chim. Acta, 1980,45,147.
[208] L.M.J. Vallarino, in: K.A. Gschneidner Jr., L. Eyring (Eds.), Handbookon the Physics and Chemistry of Rare Earths, vol. 15, Elsevier,Amsterdam, 1991, Chapter 104.
[209] A.M. Arif, J.D.J. Backer-Dirks, C.J. Gray, F.A. Hart, M.B. Hursthouse,J. Chem. Soc., Dalton Trans., 1987,1665.
[210] (a) L. De Cola, D.L. Smailes, L.M. Vallarino, Inorg. Chem., 1986,25,1729; (b) K.K. Fonda, L.M. Vallarino, Inorg. Chim. Acta, 2002, 334,403.
[211] G. Bombieri, J. Alloys Compd., 1997,249, 76.
[212] T.W. Bell, F. Guzzo, M.G.B. Drew, J. Am. Chem. Soc, 1991,113, 3121.
[213] J.R. Morrow, L.A. Buttery, V.M. Shelton, K.A. Berback, J.Am.Chem.Soc, 1992,114, 1903.
[214] N. Hayashi, N. Takeda, T. Shiiba, M. Yashiro, K. Watanabe, M.Komiyama, Inorg. Chem, 1993,32,5889.
[215] D.A. Voss Jr., L.A. Buttrey-Thomas, T.S. Janik, M.R. Churchill,J.R. Morrow, Inorg. Chim. Acta, 2001, 317,149.
[216] L. M. Vallarino, J. Alloys Compd., 1997,249,69.
[217] (a)F. Benetollo, G. Bombieri, W.A. Gootee, K.K. Fonda, K.M.Samaria, L.M. Vallarino, Polyhedron, 1998,17, 3633; (b) F. Benetollo, G. Bombieri, A.M. Adeyga, K.K. Fonda, W.A.Gootee, K.M. Samaria, L.M. Vallarino, Polyhedron, 2002,21,425.
[218] S. Kobayashi, T. Hamada, S. Nagayama, K. Manabe, Org. Lett, 2001,3,165.
[219] T. Hamada, K. Manabe, S. Ishikawa, S. Nagayama, M. Shiro, S.Kobayashi, J. Am. Chem. Soc, 2003, 125,2989.
[220] T. Tsubomura, K. Yasaku, T. Sato, M. Morita, Inorg. Chem, 1992,31,447.
[221] S.W.A. Bligh, N. Choi, E.G. Evagorou, W.-S. Li, M. McPartlin,Chem. Commun, 1994, 2399.
[222] A. Lachgar, K.S. Coates, S.C. Jackels, Inorg. Chem, 1994,33,2219.
[223] L.H. Bryant Jr., A. Lachgar, S.C. Jackels, Inorg. Chem., 1995,34,4230.
[224] J. Lisowski, P. Starynowicz, Polyhedron, 2000,19,465.
[225] J. Lisowski, P. Starynowicz, Inorg. Chem. Commun., 2003,6, 593.
[226] J. Mazurek, J. Lisowski, Polyhedron, 2003,22,2877.
[227] N.H. Pilkington, R. Robson, Aust. J. Chem., 1970,23,2225.
[228] H. Okawa, S. Kida, Bull. Chem. Soc. Jpn., 1972,45, 1759.
[229] B. F. Hoskins, R. Robson, G.A. Williams, Inorg. Chim. Acta, 1976,16,121.
[230] L.K. Thompson, S. K. Mandal, S.T. Tandon, J.N. Bridson, M.K.Park, Inorg. Chem., 1996,35,3117.
[231] A. Asokan, B. Varghese, A. Caneschi, P.T. Manoharan, Inorg.Chem., 1998, 37,228.
[232] H. Wada, K. Motoda, M. Ohba, H. Sakiyama, N. Matsumoto, H.~-Okawa, Bull. Chem. Soc. Jpn., 1995,68,1105.
[233] H.-R. Chang, S.K. Larsen, P.D.W. Boyd, C.G. Pierpont, D.N. Hendrickson ,J. Am. Chem. Soc, 1988,110,4565.
[234] R.R. Gagne, C.L. Spiro, T.J. Smith, C.A. Hamann, W.R. Thies,A.K. Shiemke, J. Am. Chem. Soc, 1981,103,4073.
[235] S.K. Dutta, J. Ensling, R. Werner, U. Florke, W. Haase, P. Gutlich,K. Nag, Angew. Chem. Int. Ed., 1997,36,152.
[236] A. Asokan, B. Varghese, A. Caneschi, P.T. Manoharan, Inorg. Chem., 1998,37,228.
[237] A.J. Atkins, A.J. Blake, M. Schroder, J. Chem. Soc, Chem. Commun., 1993,353.
[238] A.J. Atkins, D. Black, A.J. Blake, A. Marin-Becerra, L. Ruiz-Ramirez, M. Schroder, J. Chem. Soc, Chem. Commun., 1996,457.
[239] A.J. Atkins, D. Black, R.L. Finn, A. Marin-Becerra, A.J. Blake,L. Ruiz-Ramirez, W.-S. Li, M. Scr¨oder, Dalton Trans., 2003,1730.
[240] B. Dutta, B. Adhikary, P. Bag, U. F16rke, K. Nag, J. Chem. Soc,Dalton Trans., 2002, 2760.
[241] P. Starynowicz, J. Lisowski, Chem. Commun., 1999,769.
[242] M. Tadakoro, H. Sakiyama, N. Matsumoto, M. Kodera, H. Okawa,J. Chem. Soc, Dalton Trans., 1992,313.
[243] S. S. Tandon, V. McKee, J. Chem. Soc, Dalton Trans., 1989,19.
[244] N.A. Bailey, D.E. Fenton, P.B. Roberts, A.M. Walford, J. Chem.Soc, Dalton Trans., 1987,1865.
[245] M. Botta, U. Casellato, C. Scalco, S. Tamburini, P. Tomasin, P.A. Vigato, S. Aime, A. Barge, Chem. Eur. J., 2002, 8,3917.
[246] A. Caneschi, L. Sorace, U. Casellato, P. Tomasin, P.A. Vigato, Eur. J. Inorg. Chem., 2004, 3887.
[247] M. Sakamoto, K. Manaseki, H. (?)kawa, Coord. Chem. Rev., 2001, 379, 219.
[248] J. Lisowski, P. Starynowicz, Inorg. Chem., 1999, 38, 1351.
[249] J. Lisowski, P. Starynowicz, Polyhedron, 1999, 18, 443.
[250] J. Lisowski, Unpublished results.
[251] S.S. Tandon, L.K. Thompson, J.N. Bridson, Chem. Commun., 1992, 911; S.S. Tandon, L.K. Thompson, J.N. Bridson, C. Benelli, Inorg.Chem., 1995, 34, 5507.
[252] F.Avecilla, R.Bastida, A. De Bias, D.E. Fenton, A.Mayas, A.Rodryguez, T. Rodryguez-Blas, S.Garcia-G-randa, R Corzo-Suarez, J. Chem. Soc.,Dalton Trans., 1997, 409.
[253] F. Avecilla, A. De Bias, R. Bastida, D.E. Fenton, J. Mah'ya, A.Mac'yas, C. Platas, A. Rodr'yguez, T. Rodr'yguez-Blas, Chem. Commun., 1999, 125.
[254] Q. Zeng, S. Gou, L. He, Y. Gong, X. You, Inorg. Chim. Acta, 1999, 287, 14.
[255] C. Platas, F. Avecilla, A. De Bias, C.F.G.C. Geraldes, T. Roddguez-Blas, H. Adams, J. Mahia, Inorg. Chem., 1999, 38, 3190.
[256] Q.-Y. Chen, Q.-H. Luo, Z.-L. Wang, J.-T. Chen, Chem. Commun., 2000, 1033.
[257] Q.-Y. Chen, Q.-H. Luo, D.-G. Fu, J.-T. Chert, J. Chem. Sot., Dalton Trans., 2002, 2873.
[258] X.-L. Hu, M.-C. Shen, J.-T. Chen, Chem. Eur. J., 2002, 8, 3984.
[259] F. Avecilla, C. Platas-Iglesias, R. Rodryguez-Cortinas, G. Guillemont,J.-C.G. Bünzli, C.D. Brondino, C.F.G.C. Geraldes, A. DeBlas, T. Rodryguez-Blas, J. Chem. Soc., Dalton Trans., 2002, 4658.
[260] R. Rodryguez-Corti(?)as, F. Avecilla, C. Platas-Iglesias, D. Imbert,J.-C.G. Bünzli, A. De Bias, T. Rodr'yguez-Blas, Inorg. Chem., 2002, 41, 5336.
[261] Q.-Y. Chen, Q.-H. Luo, L.-M. Zheng, Z.-L. Wang, J.-T. Chen, Inorg. Chem., 2002, 41,605.
[262] S.R. Korupoju, N. Mangayarkarasi, S. Ameerunisha, E.J. Valente,P.S. Zacharias, J. Chem. Soc., Dalton Trans., 2000, 2845.
[263] S.R. Korupoju, N. Mangayarkarasi, P.S. Zacharias, J. Mizuthani,H. Nishihara, Inorg. Chem., 2002, 41, 4099.
[264] N. Kuhnert, G.M. Rossignolo, A.Lopez-Periago, Org. Biomol.Chem., 2003, 1, 1157.
[265] N.Raman, A.Kulandaisamy, A. Shunmugasundaram, K. Jeyasubramanian, Transition Met. Chem., 2001, 26, 131.
[266] R. S. Srivastava, Inorg. Chim. Acta., 1981, 56, 65.
[267] N. Gupta, R. Swaroop, R. V. Singh, Main Group Met. Chem., 1997, 14, 387.
[268] (a) L. Mishra, V. K. Singh, Indian J. Chem., 1997, 32A, 446; (b) R. Malhotra, S. Kumar, Dhindsa, K. S. Indian, J. Chem., 1993, 32A, 457; (c) W. Levinson, E. Jawetz, Med. Microbiol. Immunol., 4th edit., Stamford, 1996.
[269] H. Smit, et al., Antimicrobial Agents and Chenetherapy, 1982, 21,881
[270] B. M. Aritic, et al., Europ. J. Med. Chem., 1977,12, 573
[271] E. M. Hodnett, W. J. J. Dunn, Med. Chem. 1970, 13, 768.
[272] 陈德余，张义建，张平等，应用化学，2000，17，607
[273] 张建民，李瑞芳，无机化学学报，1999，15，493
[274] 叶勇．湖北大学学报，2001，23，57．
[275] T. R. Younkin, E. F. Connor, R. H. Grubbs, et al., Sc., 2000, 287, 460
[276] S. Matsui, T. Fujita, Catalysis Today, 2001, 66, 63
[277] L. K. Johnson, C. M. Killian, M. Brookhart, et al., J. Am. Chem.Soc.,1995, 117, 6415
[278] Small B L, Brookhart M, Bennett A M A, et al., J Am. Chem.Soc., 1998, 120, 4049
[279] Britovsek G J P, Bruce M,Gibson V C, et al., J Am. Chem.Soc., 1999, 121, 8727
[280] B. L. Small, M. Brookhart, J. Am. Chem.Soc., 1998, 120, 7143
[281] L. S. Cai, H. Mahmoun, Y. Han, Tetrahedron: Asymmetry, 1999, 10, 411.
[282] 仇敏，刘国生，姚小泉等，催化学报，2001，22，77．
[283] 李琛，张维萍，姚小泉等．催化学报，2000，21，289．
[284] Z.G. Li, Z. Zhuo, B.S.Wan, et al., Journal of molecular Catalysis A: Chemical, 2001, 165, 67.
[285] H.-W. Wang, W. Sun, C.-G. Xiao, J. Mol. Catal. A: Chem., 2003, 206, 199.
[286] Z.-N Li, G.-S. Liu, Z. Zheng, et al., Tetrahedron, 2002, 56, 7187.
[287] L. J. Therior, G. O. Carlisle, H. J. Hu, J. Inorg. Nucl. Chem., 1969, 31, 2841
[288] 彭清静，傅伟吕，邹晓勇等，化学世界，2001，10，539．
[289] 范谦，黎耀忠，程克梅等，四川大学学报(自然科学版)，2001，38，230．
[290] H. Ma, S.-H. Chen, L. J. Niu, Electrochem. Soc., 2001, 148, 208.
[291] 李晓常，孙景志，马於光，高等学校化学学报，1999，20，309。
[292] X.-Z.You, W.-H.Feng, J. Chem. Soc. Chem. Commun., 1994, 2391.
[293] 田颜清，林凤，赵英英等，应用化学，1993，12，90。
[294] 程鹏，廖代正，阎世平等，中国科学(B辑)，1996，26，97。
[295] D. B. Wang, B. H. Chen, Y. X. Ma, Syn. React. Inorg. Met.-Org. Chem., 1997, 27, 479.
[296] Z. H. Chohan, A. Rauf, Syn. React. Inorg. Met.-Org. Chem., 1996, 26, 591.
[1] Bruker, SMART (Version 5.628) and SAINT (Version 6.02). Bruker AXS Inc., Madison, Wisconsin, USA., 1998.
[2] G. M. Sheldrick, SADABS. Program for Multi-scan Absorption Correction of Area Detector, University of G(?)ttingen, Germ., 1996.
[3] G. M. Sheldrick, SHELXTL V5.1 Software Reference Manual, Bruker AXS, Inc., Madison, Wisconsin, USA., 1997.
[4] X. Chen, C. Plasencia, Y. Hou, N. Neamati, J. Med. Chem. 2005, 48, 1098.
[5] H.-Q. Li, H.-M. Ge, Y.-X.i Chen, L. Shi, H. Ding, H.-L. Zhu, and R.-X. Tan, Chem. Biodivers., 2006, 3,463.
[1] Paola V., Matteo I., Irini A. D., Paolo L. C., Bernadetta B., Roberta L., Eur. J. Med. Chem., 2006, 41,624..
[2] Timothy B. Chaston, Des R. Richardson, J Biol Inorg Chem, 2003, 8, 427.
[3] Patricia M., Virginie L., Christian S., and Philippe G., Bioorg. & Med. Chem. Let., 2006, 16,31.
[4] Rosanna Maccari, Rosaria Ottana and Mafia Gabriella Vigorita, Bioorg. & Med. Chem. Let., 2005, 15, 2509.
[5] Dharmarajan Sriram, Perumal Yogeeswari and Kasinathan Madhu, Bioorg. & Med. Chem. Let., 2006, 16, 876.
[6] Rando D.G., Doriguetto A.C., Tomich de Paula da Silva C.H., Ellena J., Sato D.N. Leite,C.Q.F., Varanda E. A., Ferreira E.I., Eur. J. Med. Chem., 2006, 41, 1196.
[7] Bao-dui Wang, Zheng-Yin Yang and Tian-rong Li, Bioorg. & Med. Chem. Let. 2006, 14, 6012.
[8] Xu C., Mao H. Y., Zhang H. Y., Liu H. L., J. Mol. Struct., 2003, 658, 59.
[9] P. Melnyk, V. Leroux, C. Sergheraert, P. Grellier, Bioorg. Med. Chem.Lett., 2006, 16, 31.
[10] D.G. Rando, D.N. Sato, L. Siqueira, A. Malvezzi, C.Q.F. Leite, A.T. Amaral, E.I. Ferreira, L.C. Tavares, Bioorg. Med. Chem., 2002, 10, 557.
[11] J. Patole, U. Sandbhor, S. Padhye, D.N. Deobagkar, C.E. Anson, A.Powell, Bioorg. Med. Chem. Lett., 2003, 13, 51.
[12] R. Maccari, R. Ottana, M.G. Vigorita, Bioorg. Med. Chem. Lett., 2005, 15, 2509.
[13] N. Georgieval and V. Gadjeva, Biochemistry-moscow+,, 2002, 67, 705.
[14] E.M. Sah., D.J. Drain, M. Seiler, J. Pharm. Pharmacol. 1952, 4, 844.
[15] S. Rollas, N. Gu¨lerman, H. Erdeniz, Farmaco, 2002, 57, 171.
[16] S. Güniz Kücükgüzel, Adil Mazi, Fikrettin Sahin, Suzan (?)ztürk, James Stables, Eur. J. Med. Chem., 2002, 37, 197.
[17] S. Güniz Kücükgüzel, Adil Mazi, Fikrettin Sahin, Suzan (?)ztürk, James Stables, Eur. J. Med. Chem., 2003, 38, 1005.
[18] X. Chen, C. Plasencia, Y. Hou, N. Neamati, J. Med. Chem., 2005, 48, 1098.
[1] T.R. Frieden, T. R. Sterling, S. S.Munsi., C. J. Watt, C. Dye, Lancet, 2003, 362, 887.
[2] C. S. Currie, B. G. Williams, R. C. Cheng, C. Dye, AIDS, 2003, 17, 2508.
[3] B. G. Williams, C. Dye, Sci., 2003, 301, 1537.
[4] Z. Toossi, H. Mayanja-Kizza, C. S. Hirsch, K. L.Edmonds, T. Spahlinger, D. L. Hom, H. Aung, P. Mugyenyi, J. J. Ellner, C. W.C. Whalen., Exp. Immunol, 2001, 123, 8.
[5] J. A. Sbarbaro, Chest 1997, 111, 1151.
[6] R.J. Coker, Public Health, 2003, 117, 281.
[7] P. S. J. Floriano, E. Javier, L. F. Marcelle de., Y. P. Mascarenhas, M. V.N. de Souza, T. R.A. Vasconcelos, J. L. Wardell, S. M.S.V. Wardell, J. Mol. Struct., 2006, 788, 63.
[8] I. A. Blair, R. M. Timoco, M. J. Brodie, R. A. Clare, T. Dollery, J. A Timbrell, I. A.Beever Hum., Toxicol., 1985, 4, 202.
[9] G. L. Mondell, M. A. Sande, In The Pharmacological Basis of Therapeutics, A. G.Gilman, T. W.Rull, Eds., 8th ed.; Pergamon Press: New York, 1991, p1147.
[10] W. J. Wechter, M. A. Johnson, C. M. Hall, D. T. Warner, A. E. Berger, A. H. Wenzel, D. T.Gish, G. L. Neil, J. Med. Chem., 1975, 18, 344.
[11] R. Maccari, R. Ottana, F. Monforte, M. G. Vigorita Antimicrob, Agent Chemother., 2002, 46, 294.
[12] E. Szarvasi, L. Fontaine, A. Betbeder-Matibet, J. Med. Chem., 1973, 16, 281.
[13] H.M. Eisa, A.S. Tantawy, M.M. El-Kerdawy, Pharmazie, 1991, 46, 182.
[14] M.A. Khalil, O.A. El-Sayed, H.A. El-Shamy, Arch. Pharm., 1991,182. 4 N. Ulusoy, G. C, apan, G. ou tu k, M. Kiraz, Boll. Chim., Farmac, 2000,139,167.
[15] N. Ulusoy, N. Ergenc, G.o tuk, M. Kiraz, Boll. Chim., Farmac, 2001,140,417.
[16] S. Rollas, N. Gulerman, H. Erdeniz, Farmaco, 2002, 57,171.
[17] S.G. Kuc.ukgu zel, E.E. Oruc, S. Rollas, F. Sahin, A. ozbek, Eur. J. Med. Chem., 2002, 37,197.
[18] N. Ulusoy, N. Ergenc,, A.C. Ekinci, H. o zer, Monatsh. Chem., 1996, 127,1197.
[19] B.C.akir, E. Yildirim, T. Ercanli, K. Erol, M.F. Sahin, Farmaco, 1999, 54, 842.
[20] J.R. Dimmock, S.C. Vashishtha, J.P. Stables, Eur. J. Med. Chem, 2000, 35,241.
[21] S.N.Pandeya, H. Manjula, J.P. Stables, Pharmazie, 2001, 56,121.
[22] E.M. Sah., D.J.Drain, M. Seiler, J. Pharm. Pharmacol, 1952,4, 844.
[23] J.M. Patel, M.P. Dave, N.A. Langalia, K.A. Thaker, J. Indian Chem. Soc, 1984,61,718.
[24] L. Bukowski, M. Janowiec, Pharmazie, 1996,51,27.
[25] S.G. K c.ukgu zel, S. Rollas, I. Kuc.ukgu zel, M. Kiraz, Eur. J Med. Chem., 34,1999,1093.
[26] L. Bukowski, M. Janowiec, Z. Zwolska-Kwiek, Z. Andrzejczyk, Pharmazie, 1999,54,651.
[27] Joshi C., Khosla N., Tiwari P. Bioorg., Med. Chem., 2004,14,571.
[28] D. Sriram, P. Yogeeswari and K. Madhu Bioorg. & Med. Chem. Lett., 2005,15,4502.
[29] H. Smit,et al., Antimicrob. Agents Ch., 1982,21, 881
[30] B. M. Aritic, et al, Europ. J. Med. Chem., 1977,12, 573
[31] N.Gupta, R. Swaroop, R. V. Singh, Main Group Met. Chem., 1997,14,387.
[32] L.Mishra, V. K. Singh, Indian J Chem, 1997,32A, 446.
[33] R. Malhotra, S. Kumar, K. S. Dhindsa, Indian J. Chem, 1993,32A, 457.
[34] W. Levinson, E. Jawetz, Med. Microbiol. Immun, 4th edit, Stamford, 1996.
[1] S.Adsule, V. Barve, D. Chen, F.Ahmed, Q. P.Dou, S. Padhye, F.H. Sarkar, J. Med. Chem., 2006; 49(24), 7242-7246.
[2] T. Ota, Y. Furutani, A. Terakita, Y. Shichida, H. Kandod, Biochem. 2006; 45(9), 2845-2851.
[3] M. Shibata, H. Kandori, Biochemistry, 2005, 44(20), 7406-7413.
[4] B. Thati, A. Noble, B. S. Creaven, M. Walsh, M. McCann, K. Kavanagh, M. Devereux, D. A. Egan, Cancer Letters, 2007, 248, 321-331
[5] D. Sriram, E Yogeeswad and R. V. Devakaram, Bioorg. Med. Chem., 2006, 14, 3113-3118.
[6] R. Herchel, R. Boca, M. Gembicky, K. Falk, H. Fuess, W. Haase, I. Svoboda, Inorg. Chem., 2007; 46(5); 1544-1546.
[7] T. Tanaka, Y.Yasuda, M. Hayashi, J. Org. Chem. 2006; 71(18), 7091-7093.
[8] R.Herchel, R. Boca, M. Gembicky, K. Falk, H. Fuess, W. Haase, I. Svoboda, Inorg. Chem., 2007; 46(5), 1544-1546.
[9] S. Handa, V. Gnanadesikan, S. Matsunaga, M. Shibasaki, J. Am. Chem. Soc., 2007, 129(16), 4900-4901.
[10] E. R. Jarvo, B. M. Lawrence, E. N. Jacobsen, Angew. Chem., 2005, 117, 6197-6200
[11] M. Zhao, C. Zhong, C. Stem, A. G. M. Barrett, B. M. Hoffman, J. Am. Chem. Soc., 2005; 127(27), 9769-9775.
[12] E. Jabri, M. B. Carr, R. P.Hausinger, et al. Sci., 1995, 268, 998.
[13] Z.-L. You, H.-L. Zhu, Z. Anorg. Allg. Chem., 2006, 632, 140.
[14] A. Panja, N. Shaikh, S. Gupta, R. J. Butcher, P. Banerjee, Eur. J. Inorg. Chem., 2003, 1540.
[15] H.-L. Zhu, Y.-X. Tong, X.-M. Chen, J. Chem. Soc., Dalton Trans., 2000, 4182.
[16] 肖子敬，刘世雄，林墀昌，无机化学学报，2004，20，513。
[17] Gupta, N., Swaroop, R., Singh, R. V. Main Group Met. Chem., 1997, 14, 387.
[18] (a) L. Mishra, V. K. Singh, Indian J. Chem., 1997, 32A, 446; (b) R. Malhotra,, S. Kumar, K. S. Dhindsa, Indian J. Chem., 1993, 32A, 457; (c) W. Levinson, E. Jawetz, Med.1 Microbiol. Immunol., 4th edit., Stamford, 1996.
[19] H. Smit, et al., Antimicrob. Agents Ch., 1982, 21,881
[20] B. M. Aritic, et al., Europ. J. Med. Chem., 1977, 12, 573
[1] T. Tanaka, Y. Yasuda, M. J. Hayashi, Org. Chem., 2006, 71(18), 7091-7093.
[2] Y. L. Qian, W. Zhao, J. L. Huang, Inorg. Chem. Commun. 2004, 7, 459.
[3] M. B. Ferrari, F. Bisceglie, G. Reffo, G.. Pelosi, P. Tarasconi, R. Albertini, A. Bonati, P. Lunghi, S. J. Pinelli, Inorg. Biochem., 2001, 83, 169.
[4] A. Okada, T. Shibuguchi, T. Ohshima, H. Masu, K. Yamaguchi, M. Shibasaki Angew. Chem. Intern. Ed., 2005, 44(29), 4564-4567.
[5] J. Ziegler, T. Schuerle, L. Pasierb, C. Kelly, A. Elamin, K. A. Cole, D. W. Wright, Inorg. Chem.; 2000, 39(16), 3731-3733.
[6] S. Adsule, V. Barve, D. Chen, F. Ahmed, Q. P. Dou, S. Padhye, F. H. Sarkar, J. Med. Chem., (Brief Article), 2006, 49(24), 7242-7246.
[7] M. Alexiou,; I. Tsivikas, C. Dendrinou-Samara, A. A. Pantazaki, P. Trikalitis, N. Lalioti, D. A. Kyriakidis, D. P. J. Kessissoglou, Inorg. Biochem., 2003, 93, 256.
[8] H. Zahid, M. Chohan, M. Arif, Appl. Organomet. Chem., 2007, 21(4), 294-302.
[9] F. M. Belicchi, F. Bisceglie, G.. Pelosi, M. Sassi, P. Tarasconi, M. Cornia, S. Capacchi, R. Albertini, S. Pinelli, J. Inorg. Biochem., 2002, 90, 113.
[10] R. Campo, J. J. Criado, E. Garcia, M. R. Hermosa, A. Jimenez-Sanchez,; J. L. Manzano, E. Rodriguez-Fernandez, F. Sanz, J. Inorg. Biochem., 2002, 89, 74.
[11] Alexiou, M.; Tsivikas, I.; Dendrinou-Samara, C.; Pantazaki, A. A.; Trikalitis, P.; Lalioti, N.; Kyriakidis, D. A.; Kessissoglou, D. P. J. Inorg. Biochem., 2003, 93, 256.
[12] S.-X. Liu, S. Lin, B.-Z. Lin, C.-C. Lin, J.-Q. Huang, 2001, Angew. Chem., Int. Ed. Engl., 40, 1084
[13] Xiao-Hua Chen, Shi-Xiong Liu Chin. J. Inorg. Chem., 2005, 21,15
[14] J.-L. Hou, X.-B. Shao, G-J. Chen, Y-X. Zhou, X.-K. Jing, Z.-T. Li, J. Am. Chem. Soc., 2004, 126, 12386.
[15] H. Smit, et al., Antimicrob. Agents Ch., 1982, 21, 881
[16] W. Levinson, E. Jawetz, Med. Microbiol. Immun., 4th edit., Stamford, 1996.
[17] S. B. Charles, M. Lesley, P. Lynn, J. D. Susan, Biochim. Biophys. Acta., 2005, 1740, 340.
[18] K. A. Irena, M. B. Georgi, Z. B. Maya, K. Margarita, Euro. J. Med., 2005, 40, 542.
[19] X. Zhong, J. Yi, J. Sun, H.-L. Wei, W.-S. Liu, K.-B. Yu, Eur. J. Med. Chem., 2006, 41, 1090.
[1] Y.-P. Tian, C.-Y. Duan, X.-Z. You, Transit. Met. Chem., 1998, 23, 17.
[2] X. H. Zhu, S. H. Liu, Y. J. Liu, J. Ma, C. Y. Duan, X. Z. You, Y. P. Tian, F. X. Xie, S. S. Ni, Polyhedron, 1998, 19, 181
[3] M. A. Ali, S. M. M. H. Majumder, R. J. Butcher, J. P. Jasinski, J. M. Jasinsld, Polyhedron, 1997, 16, 2749.
[4] M. A. Ali, M. H. Kadir, M. Nazimuddin, S. M. M. H. Majumder, M. T .H. Tarafder, M. A. Khair, Ind. J. Chem, 1988, 27A, 1064.
[5] M. A. Ali, S. E. Livingstone, Coord. Chem. Rev., 1974, 13, 101.
[6] Y.-P. Tian, C.-Y. Duan, Z.-L. LU, X.-Z. You, Polyhedron, 1996, 15, 2263.
[7] M. A. Ali, K. K. Dey, M. Nazimuddin, F. E. Smith, R. J. Butcher, J. P. Jasinski, J. M. Jasinski, Polyhedron, 1996, 5, 3331.
[8] M. A. Ali, M. Nazimuddin, R. Shaha, R. J. Butcher, J. C. Bryan, Polyhedron, 1998, 17, 3955.
[9] N. Bharti, M. R. Maurya, F. Naqvia and A. Azama, Bioorg. Med. Chem. Lett. 2000, 10, 2243-2245
[10] S. Bhattacharjee, R. Bhattacharyya, J. Chem. Soc., Dalton Trans., 1992, 1357.
[11] B. Neelama, M. R. Maurya, N. Fehmidaa, B. Alokc, B. Sudhad, A. Amira, Eur. J. Med. Chem. 2000, 35, 481-486
[12] C. Y. Duan, Y. P. Tian, X. Z. You, T. C. W. Mak, Polyhedron, 16, 1997, 4097.
[13] S. M. M. H. Majumder, M. A. Ali, F. E. Smith, M. A. U. Mridha, Polyhedron, 1995, 7, 2153.
[14] M. E. Hossain, M. N. Alam, M. A. Ali, M. Nazimuddin, F. E. Smith, R. C. Hynes, Polyhedron, 1996, 15, 973.
[15] Y.-P. Tian, C.-Y. Duan, Z.-L. Lu and X.-Z. You, Polyhedron 1996, 15, 2263-2271.
[16] M. A.r Ali, A. H. Mirza, M.i H. S.A. Hamid,. V. Bernhardt, Polyhedron, 2005, 24, 383-390
[17] B. S. A. Thahira Ravoof, A. Karen, M. Crouse, I. M. Tahir, A. R. Cowley, M. A. Alic, Polyhedron, 2007, 26, 1159-1165
[18] Z.-M. Zhong, X.-J., R. Xing, S. Liu, Z.-Y. Guo, X.-L Chena, and P. Lia, Bioorg. Med. Chem., 2007, 15, 3775-3782
[19] M. A. Ali, A. H. Mirza, M. H. S. A. Hamid, F. H. Bujang, P. V. Bernhardt, Polyhedron, 2004, 23 2405-2412.
[20] M. A. Ali, A. H. Mirza, R. J. Butcher, M. T. H. Tarafder, M.. Ali, Inorg. Chim. Acta, 2001, 320, 1-6.
[21] M. B. Ferrari, S. Capacchi, G. Pelosi, G. Reffo, P. Tarasconi, R. Albertini, S. Pinelli, P. Lunghi, Inorg. Chim. Acta, 1999, 286, 134.
[22] D. L. Klaymen, J. P. Scovill, J. Bruce, J. F. Bartosevich, J. Med. Chem., 1984, 27, 87.
[23] R. Yuan, Y.-Q. Song, Y.-Q. Chai, S.-X. Xia, Q.-Y. Zhong, B. Yi, M. Ying, G.-L. Shen, R.-Q. Yu, Talanta, 1999, 48, 649-657
[24] G. M. de Lima, J. L. Nero, H. Beraldo, H. G. L. Siebald, D. J. Duncalf, J. Mol. Struct. 2002, 604, 287
[25] X.-X. Lu, S.-Y. Qin, Z.-Y. Zhou, V. W.-W. Yama, Inorg. Chim. Acta, 2003, 346 49-56
[26] R. A. Sanchez-Delgado, K. Lazardi, L. Rincort, J. A. Urbina, J. Med. Chem., 1993, 36, 2041.
[27] G. M. de Lima, J. L. Neto, H. Beraldo, H. G. L. Siebald, D. J. Duncalf, J. Mol. Struct., 2002, 604, 287.
[28] L. Mishra, J. Indian Chem. Soc., 1999, 76,175.
[29] M. A. Ali, C. M. Haroon, M. Nazimuddin, S. M. M. H. Majumder, M. T. H. Tarafder, M.A. Khair, Transition Met. Chem., 1992, 17, 133.
[30] M. A. Ali, N. E. Ibrahim, R. J. Butcher, J. P. Jasinski, J. M. Jasinski, J. C. Bryan, Polyhedron, 1998, 17, 1803.
[31] M. A. Ali, S. M. G. Hossain, S. M. M. H. Majumder, M. Nazimuddin, M. T. H. Tarafder, Polyhedron, 1987, 6,1653.
[32] M. A. Ali, R. N. Bose, J. Inorg. Nucl. Chem., 1977, 39, 265.
[33] M. A. Ali, R. N. Bose, Polyhedron, 1984, 3,517.
[34] M. T. H. Tarafder, Teng-Jin Khoo, Karen A. Crouse, A.M. Ali, B. M. Yamin, H.-K. Fun, Polyhedron, 2002, 21, 2691.
[35] M. Albota, D, Belionne, et al., Science, 1998, 281, 1653.
[36] T. Kogej, J. W. Perry,et al., Chem. Phys. Let., 1998, 298, 1.
[37] 周爱民等，安徽大学学报(自然科学版)，2002，26，76．
[38] J. W. Perry, S. R. Marder, et al., Nonlinear Optics, 1999, 21,225.
[39] S. R. Marder and S. R. Perry, [M]. New York: McGraw-Hill 2000 Yearbook Science and Technology, 2000.
[40] B. N. Cumpston, S. Ananthayel, et al., Nature, 1999, 389, 51.
[41] B. H. Cumpston, S. P. Ananthavel, et al. Nature, 1999, 398, 51.
[42] B. A. Reinhardt, L. L. Brott, et al., Chem. Mater, 1998, 10, 1863.
[43] 郁建华，田玉鹏，施鹏飞，安徽大学学报(自然科学版)，2003，27，85．
[44] K. J. Moon, H. K. Shim, et al., Macromol., 1996, 29, 681.
[45] D. M. Burland, R. D. Miller, C.-A.Walsh, Chem. Rev., 1994, 94, 31.
[46] C.-F. Zhao, C.K. Park, P.N. Prasad, et al., Chem. Mater, 1995, 7, 1237.
[47] Y.-P. Tian, C.-Y. Duan, X.-Z You, Transit. Met. Chem., 1998, 23, 17
[1] S. Handa, V. Gnanadesikan, S. Matsunaga, M. J. Shibasaki, Am. Chem. Soc., 2007;129(16); 4900-4901.
[2] N. Nimitsifiwat, E. L.Marshall, V. C. Gibson, M. R. J. Elsegood, S. H. Dale, J. Am. Chem.Soc., 2004, 126(42), 13598-13599.
[3] J. A. Riddle, S. P. Lathrop, J. C. Bollinger, D. J. Lee, Am. Chem. Soc., 2006; 128(34),10986-10987.
[4] M. Zhao, C. Zhong, C. Stern, A. G. M. Barrett, B. M. Hoffman, J. Am. Chem. Soc., 2005;127(27), 9769-9775.
[5] D. W. Roberts, A. O. Aptula, G. Patlewicz, Chem. Res. Toxicol., 2006; 19(9), 1228-1233.
[6] T. Tanaka, Y. Yasuda, M. Hayashi, J. Org. Chem., 2006, 71(18), 7091-7093.
[7] Z. Tang, X. Chen, X. Pang, Y. Yang, X. Zhang, X.Jing, Biomacromol., 2004; 5(3); 965-970.
[8] 王维群 营养学北京：高等教育出版社，2001．
[9] 赵霖，中华医学杂志，1995，75，2302．
[10] 吴嘉惠，任榕娜，营养学报，1995，17，3633．
[11] 李云，王瑞淑，营养学报，1997，19，1964．
[12] 余章机，黄时宪，西南农业学报，1997，10，815．
[13] 吴嘉惠，吴永冰，营养学报，1994，16，446．
[14] 李正及银，赵法，营养学报，1997，19，388．
[15] 吴嘉惠，徐迪雄，营养学报，1997，19，398．
[16] 徐迪雄，白家驷，第三军医大学学报，1997，19，4549．
[17] 李积胜，徐鹏霄，营养学报，1998，20，211．
[18] 孔祥英，卞修武，第三军医大学学报，1996，18，3401．
[19] 李积胜，徐鹏霄，营养学报，1997，19，3961．
[20] 盛晓阳，洪昭毅，营养学报，1994，16，115．
[21] 文建国，李玉绿，湖南医科大学学报，1996，21，2951．
[22] 罗子国，李维信，解剖学报，1999，30，861．
[23] 周藻初，许立庆，哈尔滨医科大学学报，1996，30，11．
[25] 徐艳钢，汤雪琴，中国公共卫生学报,1993，12，298
[26] 邵英，方锦，临床眼科杂志，1998，6，277。
[27] 马国东，冰雪运动，2005，4，85．
[31] X.-Y. Qiu, Ata Cryst., E62, 2006, m717.
[32] L. Tatar, D.Ulku and O. Atakol, Acta Cryst. C55, 1999, 508.
[33] Y. Chen, Acta Cryst. E62, 2006, m204..
[1] A. Escuer, G. Aromi, Eur. J. Inorg. Chem., 2006, 4721.
[35] C. Koch, A. Malassa, C. Agthe, H. Gorls, R. Biedermann, H. Krautscheid, M.Westerhausen, Z. Anorg. Allg. Chem., 2007, 633,375.
[36] A. Roth, A. Buchholz, W. Plass, Z. Anorg. Allg. Chem., 2007, 633, 383.
[37] W. R. Knapp, J. G. Thomas, D. P. Martin, M. A. Braverman, R. J. Troviteh, R. L.LaDuca, Z. Anorg. Allg. Chem., 2007, 633, 575.
[38] M. Kloskowski, D. Pursche, R.-D. Hoffmann, R. Pottgen, M. Lage, A.Hammerschmidt,T. Glaser, B. Krebs, Z. Anorg. Allg. Chem., 2007, 633, 106.
[39] F. Marandi, B. Mirtamizdoust, A. A. Soudi, V. T. Yilmaz, C. Kazak, Z. Anorg. Allg.Chem., 2006, 632, 2380.
[40] S. Sarkar, A. Mondal, M. S. El Fallah, J. Ribas, D. Chopra, H. Stoeckli-Evans, K. K.Rajak, Polyhedron, 2006, 25, 25.
[41] M. Zbiri, S. Saha, C. Adhikary, S. Chaudhuri, C. Daul, S. Koner, Inorg. Chim. Acta,2006, 359, 1193.
[42] Z.-L. You, H.-L. Zhu, Z. Anorg. Allg. Chem., 2004, 630, 2754.
[43] Z.-L. You, H.-L. Zhu, Z. Anorg. Allg. Chem., 2006, 632, 140.
[44] I. Romero, L. Dubois, M.-N. Collomb, A. Deronzier, J.-M. Latour, J. Pecaut, Inorg.Chem. 2002, 41, 1795.
[45] J. Ribas, A. Escuer, M. Montfort, R. Vicente, R. Cortes, L. Lezama, T. Rojo, Coord.Chem. Rev. 1999, 193-195, 1027.
[46] J. Tercero, C. Diaz, J. Ribas, E. Ruiz, J. Mahia, M. Maestro, Inorg. Chem., 2002, 41,6780.
[47] Y.-X. Sun, Z.-L. You, Z. Anorg. Allg. Chem., 2006, 632, 1566.
[48] Z.-L. You, Z. Anorg. Allg. Chem., 2006, 632, 664-668.
[49] Y. Ma, W. Zhang, G.-F. Xu, K. Yoshimura, D.-Z. Liao, Z.-H. Jiang, S.-P. Yan, Z. Anorg.Allg. Chem,. 2007, 633, 657-660.
[50] L.-N. Zhu, N. Xu, Y. Yang, D.-Z. Liao, Z.-H. Jiang, S.-P. Yan, P. Cheng, Z. Anorg. Allg.Chem., 2006, 632, 2500-2504.
[51] M. Nayak, R. Koner, H.-H. Lin, U. Florke, H.-H. Wei, S. Mohanta, Inorg. Chem., 2006,45, 10764.
[52] S. Dhar, D. Senapati, P. K. Das, P. Chattopadhyay, M. Nethaji, A. R. Chakravarty, J.Am. Chem. Soc. 2003, 125, 12118.
[1] J. F. Stevens, A. W. Taylor, G. B. Nickerson, M. Ivancic, J. Henning, A. Haunold, M. L.Deinzer, Phytochemistry, 2000, 53, 759.
[2] S. Shibata, Anti-tumorigenic chalcone. Stem. Cell., 1994,12, 44.
[3] M. A. Devi, N.P. Das, Cancer Lett., 1993, 69, 191..
[4] K. Zhang, N.P.Das, Biochem. Pharmacol, 1994, 47, 2063.
[5] M. L Edwards, D.M. Stemerick. P. S. Sunkara, et al., J. Med. Chem., 1990, 33, 1948.
[6] H. Kagechika, E. Kawachi, Y. Hashimoto, et al. J. Med. Chem, 1989, 32, 834.
[7] B. Liasset, C. Doucern, J.C. Dore, et al. Biochem. Pharmacol, 1993, 46, 1257.
[8] Y. Inamori, K. Baba, H. Tsujibo, et al., Chem. Pharm. Bull, 1991, 39, 1604.
[9] R. Edenharder, I. Petersdorff, R. Rauscher, et al. Mutation Res., 1993, 287, 261.
[10] R. J. Miksicek, Mol. Pharmacol, 1993, 44, 37.
[11] (a) S. F. Nielsen, S. B. Christensen, G. Cruciani, A. Kharazmi, T. Liljefors, J. Med.Chem., 1998, 41, 4819; (b) R. Li, G. L. Kenyon, F. E. Cohen, X. Chen, B. Gong, J. N. Dominguez, E. Davidson, G. Kurzban, R. E. Miller, E. O. Nuzum, P. J. Rosenthal, J. H.Mckerrow, J. Meal. Chem., 1995, 38, 5031; (c) M. Liu, P. Wilairat, M. L. Go, J. Med. Chem., 2001, 44, 4443.
[12] J. Rojas, M. Paya, J. N. Dominguez, M. L. Ferranidz, Bioorg. Med. Chem. Lett., 2002, 12, 1951.
[13] (a) H. K. Hsieh, e T. H. Le, J. P. Wang, J. J. Wang, C. N. Lin, Pharm. Res., 1998, 15, 39;(b) M. A. Babu, N. Shakya, P. Prathipati, S. G. Kaskhedikar, A. K. Saxena, Bioorg. Med.Chem., 2003, 10, 4035.
[14] (a) S. K. Kumar, E. Hager, C. Pettit, H. Gurulingappa, N. E. Davidson, S. R. Khan, J.Med. Chem., 2003, 46, 2813; (b) S. Ducki, R. Forrest, J. A. Hadfield, A. Kendall, N. J.Lawrence, A. T. McGown, D. Rennison, Bioorg. Med. Chem. Lett., 1998, 8, 1051.
[15] T. P. Frandesn, B. Svensson, Plant Mol. Biol., 1998, 37,1.
[16] M. Artico, R. D. Santo, R. Costi, E. Novellino, G. Greco, S. Massa, E. Tramontane M. E. Marongiu, A. D. Montis, P. L. Colla, J. Med. Chem. 1998,41,3984.
[17] F. Herencia, M. L Ferrandiz, Ubeda A., J. N. Domynguez, J. E .Charris, G. M. Lobo, and A M. J.lcaraz, Med. Chem. Lett., 1998, 8,1169.
[18] X. Chen, C. Plasencia, Y. Hou, N. Neamati, J. Med. Chem., 2005,48,1098.
[19] E.M. Kosower, T. Miyadera, J. Med. Chem., 1972,15, 307
[20] J. F. Stevens, A. W. Taylor, G. B. Nickerson, M. Ivancic, J. Henning, A. Haunold, M. L. Deinzer, Phytochemistry, 2000, 53, 759.
[21] S. F. Nielsen, S. B. Christensen, G. Cruciani, A. Kharazmi, T. Liljefors, J. Med. Chem., 1998,41,4819;
[22] R. Li, G. L. Kenyon, F. E. Cohen, X. Chen, B. Gong, J. N. Dominguez, E. Davidson, G. Kurzban, R. E. Miller, E. O. Nuzum, P. J. Rosenthal, J. H. Mckerrow, J. Med. Chem., 1995, 38,5031.
[23] M. Liu, P. Wilairat, M. L. Go, J. Med. Chem, 2001,44,4443.
[24] J. Rojas, M. Paya, J. N. Dominguez, M. L. Ferranidz, Bioorg. Med. Chem. Lett, 2002, 12,1951.
[25] S. K. Kumar, E. Hager, C. Pettit, H. Gurulingappa, N. E. Davidson, S. R. Khan, J. Med. Chem, 2003,46,2813.
[26]S. Ducki, R. Forrest, J. A. Hadfield, A. Kendall, N. J. Lawrence, A. T. McGown, D. Rennison, Bioorg. Med. Chem. Lett, 1998, 8,1051.
[27] D. N. Dhar, J. B. Lal, J. Org. Chem. 1958, 23, 1159; S.Wattanasin, W.S. Murphy, Synthesis 1980, 8, 647.
[28] R. E. Lyle, L. P. Paradis, J. Am. Chem. Soc, 1955, 77,6667.
[29] H.K.Hsieh, T. H.Lee, J. P. Wang, J. J. Wang, C. N. Lin, Pharm. Res, 1998,15,39.
[30] M. A. Babu, N. Shakya, P. Prathipati, S. G. Kaskhedikar, A. K. Saxena, Bioorg. Med. Chem, 2003,10,4035.
[31] S. K. Kumar, E. Hager, C. Pettit, H. Gurulingappa, N. E. Davidson, S. R. Khan, J. Med. Chem, 1998,41,4161.
[32] N. H. Nam, Y. K, Y. J. You, D. H. Hong, H. M. Kim, B. Z. Ahn, Eur. J. Med. Chem, 2003,38,179.
[33] T. P. Frandesn, B. Svensson, Plant Mol. Biol, 1998, 37,1.
[34] M. Artico, R. D. Santo, R. Costi, E. Novellino, G. Greco, S. Massa, E. Tramontano, M. E. Marongiu, A. D. Montis, P. L. Colla, J. Med. Chem, 1998,41, 3984.