钌、铂硼烷簇合物的合成与结构
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
金属硼烷化学是硼烷化学的一个重要分支。从上世纪六十年代以来,硼烷化学一直是一个十分活跃的研究领域,已形成了硼烷、金属硼烷、碳硼烷、金属碳硼烷、主族元素杂硼烷及其金属衍生物等为数众多的研究领域,并展现出许多很有希望的应用前景,如溶剂萃取、催化反应、肿瘤的硼中子俘获治疗、非线性光学材料、液晶、离子选择性电极、阳离子相转移和高能电池的电解质以及主客体化学等。同时,拓扑结构理论、多面体骨架电子对理论等的提出也推动了结构化学的发展,进一步拓宽了结构化学的研究范围。因此,研究这类化合物的合成与结构在理论和实际应用上都是有意义的。
     论文主要研究了过渡金属配合物[PtCl2(PPh3)2]、[RuCl2(PPh3)3]分别与closo-[B_(10)H_(10)]~(2-)在不同的溶剂(甲醇、乙醇、叔丁醇等)、不同反应时间、不同的反应方式(回流、溶剂热)下的反应。对反应产物进行了分离和结构表征,并进行了部分反应性研究。
     本论文主要内容共分四章:
     第一章介绍了硼烷化学的发展简史和研究现状,综述了闭式(closo)硼烷[B_(10)H_(10)]~(2-)的反应性,特别关注最新进展及由此衍生的金属高硼烷簇合物的合成与结构。提出本论文的目的及意义。
     第二章研究了[PtCl2(PPh3)2]与closo-[B_(10)H_(10)]~(2-)分别在甲醇、叔丁醇及硫代乙酸/二氯甲烷中的回流反应,得到了三个十一顶巢式铂硼烷:[(PPh3)2PtB_(10)H10-9-(OCH3)-11-(H)0.5(OCH3)0.5] (1),[(PPh3)2PtB_(10)H10-9,10-(H0.7Cl0.3)2] (3),[(PPh3)2PtB_(10)H11-11-OOCCH3]·CH2Cl2 (4)。还研究了在甲醇中的溶剂热反应得到了一个巢式十一顶双铂硼烷簇合物[(PPh3)2Pt(μ-PPh2)PtB9H6-3,9,11-(OMe)3] (2),并通过元素分析、红外光谱、核磁共振谱、单晶X-射线衍射进行了表征。结构分析表明,1,3,4这三个铂硼烷簇合物的骨架基本类似,都具有巢式{PtB_(10)}骨架结构,铂原子处于开口的PtB4面上,除了与四个硼原子成键外,还与两个笼外三苯基膦配位。簇合物2具有Pt2B9多面体骨架结构,两个Pt原子位于Pt2B3面上的相邻位置,且由一个PPh2基团桥连,每个Pt原子还分别与三个B原子和一个PPh3配体中的P原子成键。
     第三章研究了[RuCl2(PPh3)3]和closo-[B_(10)H_(10)]~(2-)分别在不同溶剂中的反应。其中在乙醇中回流反应得到了阴离子型簇合物[Et4N][(PPh3)RuClB10H8(OEt)2] (5),并研究了簇合物5的反应性。其中5与二齿配体2,2’-联吡啶(bpy)发生取代反应生成[(bpy)2RuB10H8(OEt)2] (6)。簇合物5、6中一个钌和十个硼原子形成一个闭式的1:2:4:2:2堆积的{RuB10}骨架。钌原子占据闭式骨架结构的顶部,与六个形成船式构型的硼原子相连。对5和6通过红外光谱、核磁共振谱、单晶X-射线衍射进行了表征。在进一步研究过程中意外分离得到了[Et4N][(PPh3)2ClRuB12H12]·CHCl3 (7),结构分析表明,该簇合物含有分立的钌硼烷阴离子和四乙基铵阳离子,{RuB12H12}是由于合成原料[B_(10)H_(10)]~(2-)中含有少量closo-[B12H12]2-副产物,后者与[RuCl2(PPh3)3]反应生成的。Ru(II)中心与[B12H12]2-以三个B- H-Ru三中心两电子键结合。
     第四章对本论文研究的铂、钌配合物与closo-[B_(10)H_(10)]~(2-)在各种条件下反应得到的金属硼烷产物的合成与结构特点作出总结。
Boron cluster chemistry is an interesting and increasingly developing field of study that includes neutral boranes and their anions, metallaboranes, carboranes and metallacarboranes, main group heteroboranes and their metal derivatives. These compounds have provided a lot of interesting potential applications, including solvent extraction, catalysis, boron neutron capture therapy (BNCT) of tumors, nonlinear optics, liquid crystals, ion-selective electrodes, electrolytes for storage batteries and host-guest chemistry. Meanwhile, the topological theory and polyhedral skeletal electron-pair theory propelled the further development of borane chemistry and expanded the scope of structural chemistry. People have been synthesizing large number of boron clusters and modifying their bonding and reaction rules, in the hope of obtaining new boron clusters with special applications.Therefore, it is of interest to continue studying the syntheses and structures of new borane derivatives.
     This thesis describes the research on metallaborane clusters obtained from the reactions of [PtCl2(PPh3)2] or [RuCl2(PPh3)3] and closo-[B_(10)H_(10)]~(2-) under different conditions.
     The four sections of this thesis are as follows:
     In chapter 1, a general review is given to introduce the development of boron cluster chemistry in particular that of closo-[B_(10)H_(10)]~(2-), the structures of the transition metal metallaborane clusters.
     In chapter 2, the reactions of [PtCl2(PPh3)2] with closo-[B_(10)H_(10)]~(2-) in refluxing MeOH, tBuOH and CH3COSH/CH2Cl2, respectively, are described. The three eleven-vertex platinaborane products: [(PPh3)2PtB_(10)H10-9-(OCH3)-11-(H)0.5(OCH3)0.5] (1) ,[(PPh3)2PtB_(10)H10-9,10-(H0.7Cl0.3)2] (3),[(PPh3)2PtB_(10)H11-11-OOCCH3]·CH2Cl2 (4). The 1,3,4 clusters have nido 11-vertex {PtB_(10)} polyhedral skeleton, in which the Pt atom stay in the open PtB4 face, while connecting with four B atoms and two PPh3 ligands. A diplatinaborane [(PPh3)2Pt(μ-PPh2)PtB9H6-3,9,11-(OMe)3] (2) is obtained from the reaction of [PtCl2(PPh3)2] with closo-[B_(10)H_(10)]~(2-) in MeOH under solvothermal condition. Compound 2 has a nido 11-vertex {Pt2B9} polyhedral skeleton, in which two Pt atoms stay in adjacent position on the open Pt2B3 face and further bridged by a PPh2 group. Each Pt atom coordinates to three B atoms and a P atom of the PPh3 ligand. Some of these products are characterized by IR, NMR, elemental analysis and single-crystal X-ray analyses.
     In chapter 3, we studied the reactions of [RuCl2(PPh3)3] and closo-[B_(10)H_(10)]~(2-) in different solutions. The reaction in refluxing CH3CH2OH affords an anionic ruthenaborane cluster: [Et4N][(PPh3)RuClB10H8(OEt)2] (5). Compound 5 reacted with 2,2’-bipyridine to afford the ruthenaborane cluster [(bpy)2RuB10H8(OEt)2] (6). Both 5 and 6 are characterized by IR, NMR and single-crystal X-ray analyses. The clusters 5 and 6 are based on a closo-type 1:2:4:2:2 {RuB10} stack with the metal occuping the unique six-connected apical position and can be considered as having isocloso structures derived from the complete capping of the open face of an arachano geometry to give a completely closed deltaheral cluster. [Et4N][(PPh3)2ClRuB12H12]·CHCl3 (7) was unexpectedly isolated from above the same reaction as a red air-stable solid, in cluster 7 the integrity of the closo-[B12H12]2- is maintained and the Ru(II) center coordinates to two PPh3, a Cl- and three exo-B-H units of the closo-[B12H12]2-, with a distorted octahedral geometry.
     In chapter 4, the reactions studied using Pt and Ru complexs and closo-[B_(10)H_(10)]~(2-) under different conditions are concluded as well as the structural characters of the products.
引文
[1] Stock, A. Hydrides of Boron and Silicon. Cornell Univ:Press, New York:Ithaca, 1933.
    [2] Hermanek, S. Boron Chemistry: Introduction. Chem. Rev. 1992, 92(2), 175.
    [3] (a) Greenwood, N. N.; Earnshaw, A. Chemistry of the Elements, Oxford:Pergamon. Press, 1984. (b)唐松青,丁宏勋.硼氢化合物作为固体推进剂高燃速调节剂的最新进展,推进技术,1983, 2:35-51.
    [4] (a) Shapiro, I; Good, C. D.; Williams, R. E. The Carborane Series: BnC2Hn+2. I. B3C2H5. J. Am. Chem. Soc. 1962, 84:3837-3840. (b) Williams, R. E. Early Carboranes and Their Structural Legacy. Adv. Organomet. Chem. 1994, 36:1-55.
    [5] Greenwood, N. N.; Mcginnety, J. A. Reactions of decaborane with adducts of aluminium and gallium hydride. J. Chem. Soc. Chem. Commun. 1965, (14):331-332.
    [6] Hawthorne, M. F.; Young, D. C.; Wegner, P. A. Carbametallic Boron Hydride Derivatives. I. Apparent Analogs of Ferrocene and Ferricinium Ion. J. Am. Chem. Soc. 1965, 87(8):1818-1819.
    [7] Longuet-Higgins, H. C. Hydrogenated Substances with electron deficiencies. J. Chim. Phys. 1949, 46:268-275.
    [8] Lipscomb, W. N. The Boranes and Their Relatives, Science, 1977, 196:1047-1055.
    [9] (a) Williams, R. E. Carboranes and boranes; polyhedra and polyhedral fragments, Inorg. Chem. 1971, 10:210-214. (b) Williams, R. E. Coordination Number Pattern Recognition Theory of Carborane Structures. Adv. Inorg. Chem. Radiochem. 1976, 18:67-142.
    [10] (a) Wade, K. The structural significance of the number of skeletal bonding electron-pairs in carboranes, the higher boranes and borane anions, and various transition-metal carbonyl cluster compounds. J. Chem. Soc. Chem. Commun. 1971, (15):792-793. (b) Wade, K. Structural and Bonding Patterns in Cluster Chemistry. Adv. Inorg. Chem. Radiochem. 1976, 18:1-66.
    [11] Mingos, D. M. P. Polyhedral skeletal electron pair approach. Acc. Chem. Res. 1984, 17(9):311-319.
    [12] (a) Rudolph, R. W.; Pretzer, W. R. Hückel-type rules and the systematization of borane and heteroborane chemistry. Inorg. Chem. 1972, 11(8):1974-1978.(b) Rudolph, R. W. Boranes and heteroboranes: a paradigm for the electron requirements of clusters. Acc. Chem. Res. 1976, 9(12):446-452.
    [13] (a)卢嘉锡.原子簇化合物的结构化学.中国化学会1978年年会学术报告集.北京:科学出版社, 1981. (b)唐敖庆,李前树,吾榕之.硼烷的结构规则,化学学报,1984, 42(5):427-433. (c)陈志达,徐光宪.原子簇与有关分子的结构规则III.硼烷,碳硼烷,立方烷和棱柱烷的电子结构,化学学报,1984, 42(6):514-522. (d)张乾二,林连堂,王南钦等.多面体分子轨道的理论方法Ш,结构多面体骨架的成键分子轨道,厦门大学学报(自然科学版),1981, 20(2):226-230. (e)朱龙根,游效曾,任彤等.一些硼烷分子的自然杂化轨道研究,科学通报. 1987, (4):277-280.
    [14] Hoffmann, R. Building Bridges Between Inorganic and Organic Chemistry. Angew. Chem. Int. Ed. Engl. 1982, 21:711-717.
    [15] (a) Jemmis, E. D.; Balakrishnarajan, M. M.; Pancharatna, P. D. A Unifying Electron-Counting Rule for Macropolyhedral Boranes, Metallaboranes, and Metallocenes. J. Am. Chem. Soc. 2001, 123(18):4313-4323. (b) Jemmis, E. D.; Balakrishnarajan, M. M. Polyhedral Boranes and Elemental Boron: Direct Structural Relations and Diverse Electronic Requirements. J. Am. Chem. Soc. 2001, 123(18):4324-4330.
    [16] (a) Plesek, J. Potential applications of the boron cluster compounds. Chem. Rev. 1992, 92(2):269-278. (b) Grimes, R. N. Boron Clusters Come of Age. J. Chem. Edu. 2004, 81(5):657. (c) Valliant, J. F.; Guenther, K. J.; King, A. S. et al. The medicinal chemistry of carboranes. Coord. Chem. Rev. 2002, 232(1-2):173-230. (d) Strauss, S. H. The search for larger and more weakly coordinating anions. Chem. Rev. 1993, 93(3):927-942. (e) Reed, C. A. Carborane acids. New strong yet gentle acids for organic and inorganic chemistry. Chem. Commun. 2005, (13):1669-1677. (f) Hawthorne, M. F.; Zink, J. I.; Skelton, J. M. et al. Electrical or Photocontrol of the Rotary Motion of a Metallacarborane. Science. 2004, 303(5665):1849-1851.
    [17] Sivaev, I. B.; Bregadze, V. I.; Sj?berg, S. Chemistry of closo-Dodecaborate Anion [B12H12]2-. Collect. Czech. Chem. Commun. 2002, 67(6):679-727.
    [18] Hawthorne, M. F.; Pilling, R. L.; Knoth, W. H. Bis(triethylammonium) Decahydrodeca- borate(2-). Inorg. Synth. 1967, 9(3):16-19.
    [19] Bobrott, R. D.; Lipscomb, W. N. Structure of Cu2B10H10. J. Chem. Phys. 1962, 37(8):1779-1784.
    [20] (a) Muetterties, E. L. ; Knoth, W. H. Eds. Polyhedral Boranes, Marcel Dekker, New York, 1968. (b) Muetterties, E. L. Ed. Boron Hydride Chemistry, Academic Press, New York, 1975. (c) Kennedy, J. D. The Polyhedral Metallaboranes. Prog. Inorg. Chem. 1986, 34:211-434.
    [21] Makhlouf, J. M.; Hough, W. V.; Hefferan, G. T. Practical synthesis for decahydrodecaborates. Inorg. Chem. 1967, 6(6):1196-1198.
    [22] (a)张国敏,祝虹.硼化合物的研究(I).合成十硼十氢阴离子(B10H102-)的新方法,化学学报,1978, 36(4):315. (b)张国敏,祝虹,丁强.硼化合物的研究П,硼氢化钾与四乙基铵热解合成B10H102-的反应机理,武汉大学学报(自然科学版),1981, 2:101-102. (c) Power, D.; Spalding, T. R. Some comments on the mechanism of the preparation of (Et4N)2B10H10 by thermolysis of Et4NBH4. Polyhedron. 1985, 4(7):1329-1331.
    [23] (a) King, R. B. Three-Dimensional Aromaticity in Polyhedral Boranes and Related Molecules. Chem. Rev. 2001, 101(5):1119-1152. (b) Chen, Z.; King, R. B. Spherical Aromaticity: Recent Work on Fullerenes, Polyhedral Boranes, and Related Structures. Chem. Rev. 2005, 105(10):3613-3642.
    [24] Leites, L. A. Vibrational spectroscopy of carboranes and parent boranes and its capabilities in carborane chemistry. Chem. Rev. 1992, 92(2):279-323.
    [25] Nguyen, M. T.; Matus, M. H.; Dixon, D. A. Heats of Formation of Boron Hydride Anions and Dianions and Their Ammonium Salts [BnHmy-][NH4+]y with y = 1?2. Inorg. Chem. 2007, 46(18):7561-7570.
    [26]张国敏,祝虹,丁强.硼化合物的研究Ⅹ. B10H102-、B10H122-及B3H8-双二茂铁季铵盐及环状二茂铁季铵盐的合成.应用化学,1985, 2(1):70-73.
    [27] (a)张伦,丁自荣,张国敏.稀土硼氢化合物的研究(Ⅳ)—十氢十硼酸氧化吡啶合稀土(Ⅲ)配合物.高等学校化学学报,1986, 7(10):877-880. (b)王殿勋,李二成,徐广智等.稀土元素-吡啶氧正离子硼氢配合物的XPS伴峰及其价带谱研究.物理化学学报,1991, 7(2):234-237.
    [28]胡培植,张伦,刘夕炎等.稀土金属硼氢化物的研究(Ⅸ)—N,N’-双(邻羟基苯叉)-1,3-丙二胺合稀土(Ⅲ)十氢十硼酸盐的合成.高等学校化学学报,1988, 9:954-956.
    [29] (a) Kraus, F. Albert, B. Synthesis and Crystal Structure of Cesium Hexamminesodium Decahydro-closo-decaborate-Ammonia(1/1), Cs[Na(NH3)6][B10H10]·NH3. Z. Anorg. Allg. Chem. 2005, 631(1):152-154. (b) Kraus, F.; Korber, Nikolaus. K2Li(NH2)3 and K2Na(NH2)3—synthesis and crystal structure of two crystal chemically isotypic mixed-cationic amides. J. Solid State Chem. 2005, 178(4):1241-1246.
    [30] (a) Hofmann, K.; Albert, B. Crystal Structure of Bis(triethylammonium) closo-decahydro- decaborate, [(C2H5)3NH]2[B10H10]. Z. Naturforsch. 2000, 55b(6):499-503. (b) Hofmann, K.; Albert, B. Crystal structures of M2[B10H10] (M = Na, K, Rb) via real-space simulated annealing powder techniques. Z. Kristallographie. 2005, 220(2):142-146.
    [31] Virovets, A. V.; Vakuienko, N. N.; Volkov, V. V. et al. Crystal structure of di(1-n- dodecylpyridine)decahydro-closo-decaborate(2-) (C5H5N-C12H25)2[B10H10]. J. Struct. Chem. 1994, 35(3):339-344.
    [32] Chtsaz, S.; Follkerts, H.; Grebe, J. et al. Die Kristallstrukturen einer Serie von Verbindungen mit Kationen des Typs [R3PNH2]+, [R3PN(H)SiMe3]+ und [R3PN(SiMe3)2]+. Z. Anorg. Allg. Chem. 2000, 626(3):775-783.
    [33] Orlova, A. M.; Mustyatsa, V. N.; Goeva, L. V. et al. Dipyridine Salts of closo-Borate Anions B6H62- and B12H122- . Russ. J. Inorg. Chem. 1996, 41(10):1525-1530.
    [34] Kaster, S. B.; Malinina, E. A.; Mustyatsa, V. N. et al. Crystal structure of bis(tri- methylammonium)decahydrodecaborate(2-) and bis(dimethylammonium) dodecahydrododeca- borate(2-)bis(DMF). Three-centered bonds in closo-borane anions. Koord. Khim. 1992, 18(4):387-393.
    [35] Chantler, C. T.; Maslen, E. N. Charge transfer and three-centre bonding in monoprotonated and diprotonated 2,2'-bipyridylium decahydro-closo-decaborate(2-). Acta Crystallogr. Sect. B. 1989, 45:290-297.
    [36] Polyakova, I. N.; Mustyatsa, V. N.; Zhizhin, K. Yu. et al. Structure of the Undeca- hydrodecaborate Anion B10H11-. Crystal Structures of [Ph3PCH2Naph]B10H11 and [Ph3PEt]2B10H10 . Kristallografiya, 2004, 49(5):767-771.
    [37] Malinina, E. A.; Solntsev, K. A.; Butman, L. A. et al. Closo-Decaborate anion as acido ligand in lead coordination compounds. Koord. Khim. 1989, 15:1039-1043.
    [38] (a) Hertler, W. R.; Knoth, W. H.; Hertler, H. et al. Chemistry of Boranes. XXIV. Carbonylation of Derivatives of B10H102- and B12H122- with Oxalyl Chloride. Inorg. Chem. 1965, 4(3):288-293. (b) Shelly, K.; Knobler, C. B.; Hawthorne, M. F. Synthesis of Monosubstituted Derivatives of closo-Decahydrodecaborate(2-). X-Ray Crystal Structures of [closo-2-B10H9CO]- and[closo-2-B10H9NCO]2-. Inorg. Chem. 1992, 31:2889.
    [39] Nachtigal, C.; Preetz, W. Darstellung, 11B-NMR-, Schwingungsspektren und Kristallstruktur von Bis(tetraphenylphosphonium)-2-[2-(2-pyridylamino)pyrid-5-yl]-closo-decaborat, [P(C6H5)4]2[2-{2-(2-(C5H4N)-NH)-(C5H3N)-5}B10H9]. Z. Naturforsch. 1996, 51b:1559.
    [40] Sivaev, I. B.; Votinova, N. A.; Bragin, V. I. et al. Synthesis and derivatization of the 2-amino-closo-decaborate anion [2-B10H9NH3]? . J.Organomet. Chem. 2002, 657(1):163-170.
    [41] Ng, L. L.; Ng, B. K.; Shelly, K. et al. Structural analysis of [Et3NH][Cu(1-B10H9N2)2] and [Et3NH][1-B10H9N2]. Inorg. Chem. 1991, 30(22):4278-4280.
    [42] Naoufal, D.; Grüner, B.; Bonnetot, B. et al. Replacement of the nitrogen of [1-N2B10H9]? by amines or nitriles, a route to hydrophobic monoanions. Polyhedron. 1999, 18(7):931-939.
    [43] Naoufal, D.; Bonnetot, B.; Mongeot, H. Thermal stability of the diazohydroborate [1-N2B10H9]-: degradation to [B20H18]2- anion. Appl. Organomet. Chem. 2003, 17(4):244-246.
    [44] (a)朱伟明,张国敏,张伦.某些腈代及酰胺代多面体硼烷阴离子的电、热性质.云南师范大学学报,1997, 17(4):73. (b)胡培植,张伦,刘洋等.稀土硼氢化物的研究Ⅹ.含[B10H9NH2COCH=CH2]-的双苯甲酰丙酮缩1,3-丙二胺稀土(Ⅲ)配合物的研究.无机化学学报,1990, 6(2):130-135. (c) Zhizhin, K. Yu.; Mustyatsa, V. N.; Matveev, E. Yu. et al. Interaction between the Undecahydrodecaborate Anion B10H11- and Acetonitrile. Russ. J. Inorg. Chem. 2003, 48:671-675.
    [45] (a) Miller, H. C.; Hertler, W. R.; Muetterties, E. L. et al. Chemistry of Boranes. XXV. Synthesis and Chemistry of Base Derivatives of B10H102- and B12H122-. Inorg. Chem. 1965, 4(8):1216-1221. (b) Dou, D.; Mavunkal, I. J.; Krause Bauer, J. A. et al. Synthesis and Structure of Triethylammonium 2-(Acetonitrile)nonahydro-closo-decaborate(1-). Inorg. Chem. 1994, 33(26):6432-6434.
    [46] Lee, H.; Jalallas, J.; Onak, T. Correlation of Experimental Structural and 11B NMR Data to Calculational Results for the [2-CH3CNB10H9]- Ion. Main Group Metal Chem. 1996, 19:1-8.
    [47] (a) Nachtigal, C.; Preetz, W. Darstellung, 11B-NMR-, Schwingungsspektren und Kristallstruktur von [(C5H5N)2CH2][1-(O2N)B10H9]. Z. Anorg. Allg. Chem. 1996, 622(12):2057-2060. (b) Nachtigal, C.; Haeckel, O.; Preetz, W. Darstellung und Kristallstrukturen von [P(C6H5)4][1-(NH3)B10H9] und Cs[(NH3)B12H11]·2CH3OH. Z. Anorg. Allg. Chem. 1997, 623(9):1385-1388.
    [48] Drozdova, V. V.; Lisovskii, M. V.; Polyakova, I. N. et al. Interaction of closo-Decaborate AnionB10H102- with Iminium Salts. Russ. J. Inorg. Chem. 2006, 51(10):1552-1560.
    [49] Nachtigal, C.; Preetz, W. Darstellung, 11B-NMR-, Schwingungsspektren und Kristallstruktur von [P(C6H5)4]2 [1,10-(O2N)2B10H8]. Z. Anorg. Allg. Chem. 1997, 623(1-6):683-686.
    [50] Nachtigal, C.; Preetz, W. Darstellung und Kristallstruktur von [P(C6H5)4][2,9-{N, N’-(2-NH- (C5H4N))}B10H8]. Z. Anorg. Allg. Chem. 1997, 623(9):1489-1491.
    [51] Nachtigal, C.; Preetz, W. Darstellung, 11B-NMR-, Schwingungsspektren und Kristallstruktur von (PPh4)[1-(NO)B10H9]. Z. Anorg. Allg. Chem. 1998, 624(2):327-330.
    [52] Stmardane, U.; Chu, S. S. C.; Hosmane, N. S. et al. A tautomeric form of tetraethylammonium 1-acrylamidononahydro-closo-decaborate(1-). Acta Crystallogr. Sect C. 1989, 45:294-297.
    [53] Jasper, S. A.; Jones, R. B.; Mattern, J. et al. Palladium-Mediated Substitution Reactions of Polyhedral Borane Anions. Inorg. Chem. 1994, 33(25):5620-5624.
    [54] (a) Yao, H.-J.; Hu, C.-H.; Dou, J.-M. et al. A Neutral Triphenylphosphine-Substituted closo-Decaborane: 1,6-(PPh3)2B10H8. Acta Crystallogr. Section C. 1998, 54, IUC9800008. (b)姚海军.金属钌、铑、钯配合物和闭式B10H102-的反应和生成的金属硼烷簇合物的结构研究[博士学位论文],上海:复旦大学,1998.
    [55] Daoud, N.; Bernard, B.; Henri, M. et al. Synthesis of Bis(diphenylphosphinio)octahydro- closo-Decaborates L2B10H8 (L = Ph2PH) and 1-(Diphenylphosphino)Nonahydro-closo- Decaborates(1-) [1-LB10H9]- (L = Ph2PH, Ph2P(OH)) by The Palladium-Catalyzed Reaction of Ph2PH with 1-Diazononahydro-closo-Decaborate(1-)[1-N2B10H9]-. Collect. Czech. Chem. Commun. 1999, 64(5):856-864.
    [56] Suponistsky, K. Yu.; Timofeeva, T. V.; Allinger, N. L. Molecular Mechanics Calculations of 10-Vertex Boron Cage Compounds. Inorg. Chem. 2000, 39(15):3140-3147.
    [57] Komura, M.; Aono, K.; Nagasawa, K. A convenient preparation of 10B-enriched B12H11SH2-, an agent for neutron capture therapy. Chem. Express. 1987, 2:173.
    [58] Zhizhin, K. Yu.; Vovk, O. O.; Malinina, E. A. et al. Interaction between a Decahydro- closo-Decaborate(2–) Anion and Aliphatic Carboxylic Acids. Russ. J. Coord. Chem. 2001, 27(9):613-618.
    [59] (a) Ernard, R.; Cornu, D.; Perrin, M. et al. Synthesis and X-ray structural characterisation of the tetramethylene oxonium derivative of the hydrodecaborate anion. A versatile route for derivative chemistry of [B10H10]2-. J. Organomet. Chem. 2004, 689(16):2581-2585. (b) Zhizhin, K. Yu.; Mustyatsa, V. N.; Malinina, E. A. et al. Interaction of closo-Decaborate Anion B10H102- with Cyclic Ethers. Russ. J. Inorg. Chem. 2004, 49(2):180-189.
    [60] Zhizhin, K. Yu.; Mustyatsa, V. N.; Malinina, E. A. et al. Reactions of the B10H102- and B10H11-Anions with N,N-Dimethylformamide and N-Methylpyrrolidone. Russ. J. Inorg. Chem. 2005, 50(1):29-34.
    [61] Bragin, V. I.; Sivaev, I. B.; Bregadze, V. I. et al. Synthesis of the 1-hydroxy-closo-decaborate anion [1-B10H9OH]2?. J. Organomet. Chem. 2005, 690(11):2847-2849.
    [62] Zhizhin, K. Yu.; Malinina, E. A.; Polyakova, I. N. et al. Acid-Catalyzed Nucleophilic Substitution in the closo-Decaborate B10H102- Anion . Russ. J. Inorg. Chem. 2002, 47:1158-1167.
    [63] (a) Knoth, W. H.; Hertler, W. R.; Muetterties, E. L. Chemistry of Boranes. XXIII. B10H9S(CH3)2- and B10H8[S(CH3)2]2. Inorg. Chem. 1965, 4(3):280-287. (b) Hall, H. D.; Ulrich, B. D.; Kultyshev, R. G. et al. Synthesis, Characterization, and Chemistry of Dimethyl Sulfide Derivatives of closo-B10H102-. Collect. Czech. Chem. Comm. 2002, 67(7):1007-1024. (c) Shore, S. G.; Hamilton, E. J. M.; Kultyshev, R. G. et al. Syntheses and chemistry of bis- and tris-mercaptoborates. Pure&Appl. Chem. 2006, 78(7):1341-1348.
    [64] Komura, M.; Nakai, H.; Shiro, M. J. Regioselective synthesis of [1-B10H9(SH)]2– and [2-B10H9(SH)]2–: potential agents for boron–neutron capture therapy of brain tumours. J. Chem. Soc. Dalton. Trans. 1987:1953-1956.
    [65] (a) Srebny, H. G.; Preetz, W. Darstellung und Charakterisierung von Thiocyanatderivaten der Hydroboratanionen B10H102- und B12H122-. Z. Anorg. Allg. Chem. 1984, 513(6):7-14. (b) Nachtigal, C.; Preetz, W. Kristallstruktur von Tetraphenylphosphonium-Mono- thiocyanatohydro-closo-Decaborat, [P(C6H5)4]2[2-(SCN)B10H9]·CH3CN. Z. Anorg. Allg. Chem. 1996. 622(3):509-512. (c) Nachtigal, C.; Preetz, W. Z. Kristallstrukturen von (PPh4)2[1-(SCN)B10H9] und (AsPh4)2[1,10-(SCN)2B10H8]. Anorg. Allg. Chem. 1997, 623(1-6):347-350.
    [66] Nachtigal, C.; Steuer, B.; Preetz, W. Selenocyanato Derivatives of Hydro-closo-borates: Syntheses and Crystal Structures of (PPh4)2[SeCN)BnHn-1] (n = 6, 10, 12). Chem. Ber. 1996, 129(12):1531-1534.
    [67] O’Dowd, C.; Kennedy, J. D.; Thornton-Pett, M. The use of Kitaigorodskii's Aufbau principle in the solid-state study of crystalline borane compounds. A preliminary account. J. Organomet. Chem. 2002, 657(1):20-39.
    [68] Crtova, A. M.; Stvaev, I. B.; Lagum, V. L. et al. Preparation and structure of bis(bipyridine)bis [(1-dimethylsulfide)-closo-decaborate(1-)] lead. Koord. Khim. 1993, 19(2):116-121.
    [69] (a)Ivanov, S. V.; Ivanova, S. M.; Miller, S. M. et al. Fluorination of B10H102- with an N-Fluoro Reagent. A New Way To Transform B-H Bonds into B-F Bonds. Inorg. Chem. 1996, 35(24):6914-6915. (b) Ivanov, S. V.; Ivanova, S. M.; Miller, S. M. et al. Synthesis, Spectroscopic Characterization, and Structure of closo-1,10-B10H8F22- and Related Fluorinated Derivatives of B10H102-. Collect. Czech. Chem. Commun. 1997, 62(8):1310-1324.
    [70] Leung H. Chemistry of deca- and dodeca-closo-borate Bearing three Exopolyhedral Sulfur Substituents: [dissertation], Columbus, Ohio: Ohio State University, 2004.
    [71] Drozdova, V. V.; Zhizhin, K. Yu.; Malinina, E. A. et al. Reaction of the closo-Decaborate Anion B10H102- with Dichloroethane in the Presence of Hydrogen Halides. Russ. J. Inorg. Chem. 2007, 52(7):996-1001.
    [72] Nachtigal, C.; Preetz, W. Dipyridiniomethane 1-Iodo-closo-decaborate, [(C5H5N)2CH2] [1-IB10H9]. Acta Crystallogr. Setion C. 1996, 52:453-455.
    [73] Preetz, W.; Nachtigal, C. Kristallstruktur von Dipyridiniomethan-Monohalogenohydro-closo- Decaboraten(2-), [(C5H5N)2CH2][2-XB10H9]; X = Cl, Br, I. Z. Anorg. Allg. Chem. 1995, 621(10):1632-1636.
    [74] (a) Einholz, W.; Vaas, K.; Wieloch, C. et al. Chemische und cyclovoltammetrische Untersuchung der Redoxreaktionen der Decahalogendecaborate closo-[B10X10]2- und hypercloso-[B10X10]- (X = Cl, Br). Kristallstrukturanalyse von Cs2[B10Br10]·2H2O. Z. Anorg. Allg. Chem. 2002, 628(1):258-268. (b) Kukina, G. A.; Serglenko, V. S.; Gall, Yu. L. et al. A novelπ-allyl complex with the closo-borate anion [(h3-C3H5)Pd(CH3CN)2]2B10Br10·C6H6. Inorg. Chim. Acta. 1980, 45:L257- L259.
    [75] (a)秦笃捷,江元生.完全型卤代硼烷的稳定性问题,化学学报,1987, 45(2):113-119. (b)于微舟,张明瑜,李晓天. BnXn~(0,2-)(X=H,Cl;n=4,6,8,9,10,12)稳定性的从头计算研究,高等学校化学学报,1994, 15(3):418-422.
    [76]张伦,胡培植,张国敏.硼化合物的研究ⅩⅦ.含Cu-H-B键的[C2H5]4NB10H10Cu和[CH3]4NB12H12Cu的合成,武汉大学学报,1989, 35:67.
    [77] Malinina, E. A.; Zhizhin, K. Yu.; Lisovskii, M. V. et al. Silver(I) and Copper(I) Complexes with the closo-Decaborate Anion B10H102- as a Ligand. Russ. J. Inorg. Chem. 2002, 47(8):1158-1167.
    [78] (a) Malinina, E. A.; Zhizhin, K. Yu.; Goeva, L. V. et al. Decahydro-closo-decaborate Anion B10H102- as an Acido Ligand in Copper(I) Complexes. Doklady Chemistry. 2001, 378(1-3):139-142. (b) Malinina, E. A.; Zhizhin, K. Yu.; Mustyatsa, V. N. et al. Copper(I) and Silver(I) closo-Decaborates with an Uncommon Geometry of the Boron Polyhedron. Russ. J. Inorg.Chem. 2003, 48(7):993-1000. (c) Polyakova, I. N.; Malinina, E. A.; Kuznetsov, N. T. Crystal Structures of Cesium and Dimethylammonium Cupradecaborates, Cs[CuB10H10] and (CH3)2NH2[CuB10H10]. Kristallografiya. 2003, 48(1), 84-91.
    [79] Nachtigal, C.; Preetz, W. Darstellung und Kristallstruktur von [P(C6H5)4]2[2-SnCl(C6H5)2B10H9]. Z. Naturforsch. 1996, 51b:1061.
    [80] Nachtigal, C.; Preetz, W. Darstellung und Kristallstruktur von [P(C6H5)4]2[2-SnCl2(C6H5)B10H9]. Z. Naturforsch. 1997, 52b:975.
    [81] Zubarev, D. Y.; Li, J.; Wang, L. S. et al. Theoretical Probing of Deltahedral closo-AuroBoranes BxAux2- (x = 5?12). Inorg. Chem. 2006, 45(14):5269-5271.
    [82] Zhizhin, K. Yu.; Malinina, E. A.; Polyakova I. N. et al. Acid-Catalyzed Nucleophilic Substitution in the closo-Decaborate B10H102- Anion. Russ. J. Inorg. Chem. 2002, 47(8):1168-1181.
    [83] Hawthorne, M. F.; Shelly, K.; Li, F. The versatile chemistry of the [B20H18]2– ions: novel reactions and structural motifs. Chem. Commun. 2002, (6):547-554.
    [84] Mustyatsa, V. N.; Votinova, N. A.; Goeva, L. V. et al. Compounds of Undecahydrodecaborate Anion B10H11-. Russ. J. Coord. Chem. 2001, 27(9):622-624.
    [85] Zhizhin, K. Yu.; Mustyatsa, V. N.; Malinina, E. A. et al. The Mechanism of Acid-Catalyzed Nucleophilic Substitution in Decahydro-closo-Decaborate(2–) Anions. Russ. J. Coord. Chem. 2001, 27(9):619-621.
    [86] Shore, S. G.; Hamilton, Ewan J. M.; Bridges, A. N. et al. The Solid State Structure of [B10H11]- and Its Dynamic NMR Spectra in Solution. Inorg. Chem. 2003, 42(4):1175-1186.
    [87] Sivaev, I. B.; Petrovskii, P. V.; Filin, A. M. et al. Regioselective hydrogen-deuterium exchange in the [B10H10]2- anion. Syntheses of [1,10-B10H8D2]2- and [2,3,4,5,6,7,8,9-B10H2D8]2-. Russ. Chem. Bull. Int. Ed. 2001, 50:1115.
    [88] Hawthorne, M. F.; Mavunkal, I. J.; Knobler, C. B. Electrophilic reactions of protonated closo-B10H102- with arenes, alkane carbon-hydrogen bonds, and triflate ion forming aryl, alkyl, and triflate nido-6-X-B10H13 derivatives. J. Am. Chem. Soc. 1992, 114(11):4427-4429.
    [89] Naoufal, D.; Kodeih, M.; Cornu, D. New method of synthesis of 6-hydroxy-nido-decaborane 6-(OH)B10H13 by cage opening of closo-[B10H10]2?. J. Organomet. Chem. 2005, 690(11):2787-2789.
    [90] Bernard, B.; Miele, P.; Naoufal, D. et al. The Interaction of the [B10H10]2- Cage with Lewis Acids and the Formation of Decaborane Derivatives by Cage-Opening Reactions. Collect. Czech.Chem. Comm. 1997, 62(8):1273-1278.
    [91] Naoufal, D.; Gruner, B.; Bonnetot, B. et al. New synthesis of B9H13L (L = weak Lewis base) from [B10H10]2- by cage opening and degradation reactions. Main Group Metal Chem. 1999, 22(2):127-129.
    [92] (a)郑培菊,金若水,卫景德.簇外羧环化的十一顶钌、铂和镍十硼烷簇合物的结构研究.复旦学报(自然科学版),1999, 38:107. (b)张伦,陈新兰,配位化学进展(第一版).游效曾,孟庆金,韩万书主编,北京:高等教育出版社, 2000. (c) Greenwood, N. N. The concept of boranes as ligands. Coord. Chem. Rev. 2002, 226(1-2):61-69.
    [93]吕一辛,黄绣云,孙粹芳等.金属硼笼化合物—闭合型(closo)铁代十一硼烷的合成.化学学报,1982, 40(2):191-193.
    [94] (a) Crook, J. E.; Elrington, M.; Greenwood, N. N. et al. A novel closo-type metallaundecaborane, [1,1-(PPh3)2-2,5-(OEt)2-1-RuB10H8], and its relationship to the‘isocloso’series of metallaborane clusters. Polyhedron, 1984, 3(7):901-904. (b) Crook, J. E.; Elrington, M.; Greenwood, N. N. et al. Two unusual closo-type ruthenaboranes: preparation, molecular structure, and nuclear magnetic resonance properties of [1,1,1-(PPh3)HCl-1-RuB9H7-3,5-(PPh3)2] and [1,1-(PPh3)2-1-RuB10H8- 2,5-(OEt)2]. J. Chem. Soc. Dalton Trans. 1985:2407-2415.
    [95] Bown, M.; Fontaine, X. L. R.; Greenwood, N. N. et al. Polyhedral Ruthenaborane Chemistry. Preparation, Molecular Structure, and N.M.R. Properties of the Mixed-Ligand Eleven-Vertex isocloso-Type Compound [1,1-(PMe3)(PPh3)-closo-1-RuB10H8-2,3-(OEt)2]. Z. Anorg. Allg. Chem. 1987, 553(10):24-34.
    [96] Nie, Y.; Hu, C.-H.; Dou, J.-M. et al. A 1,10-Phenanthroline-Ligated closo-Ruthenaundecaborane: [(C12H8N2)RuB10H8(OC2H5)2]. Acta Crystallogr. Section C. 1998, 54:1813-1815.
    [97] Hu, C.-H.; Yao, H.-J.; Jin, R.-S. et al. Crystal Structure of {(PPh3)2RuB10H8[(CH3)2CHO]2}. Chin. J. Struct. Chem. 1997, 16(4):258-262
    [98] Yao, H.-J.; Li, W.; Hu, C.-H. et al. Synthesis and Crystal Structure of {(PPh3)2Cl-RuClRu(PPh3)- B10H8OCH(CH3)2}2}. Chin. J. Struct. Chem. 1998, 17(1):13-17.
    [99] Li, X.; Yao, H.-J.; Hu, C.-H. et al. Synthesis and Crystal Structure of{(PPh3)2ClRu(μ-Cl)Ru(PPh3)B10H7OCH(CH3)2)3}·0.4(H2O). Chin. J. Struct. Chem. 1999, 18(5): 378-383.
    [100] Fontaine, X. L. R.; Greenwood, N. N.; Kennedy, J. D. et al. Homobimetallic B-frame species:[{(PPh3)2Ru}-(μ-MeCO2)3-(μ-H)2-{RuB10H7}], a unique diruthenaborane in which the metal atoms are linked by one-, two-, three-, and four-membered bridges. J. Chem. Soc. Chem. Commun. 1987, (22):1717-1718.
    [101] Yao, H.-J.; Fu, J.; Jin, R.-S. et al. Crystal Structure of [(PPh3)2(C6H5COO)RuB10H8Cl]·C5H12. Chin. J. Struct. Chem. 1995, 14(5-6):364-368.
    [102] Nie, Y.; Hu, C.-H.; Wu, Q.-J. et al. 1,2:1,3-Bis(μ-p-toluato-O:O')-1-(triphenylphosphine-P)- 1-ruthena-closo-undecaborane. Acta Crystallogr. Section C. 2000, 56:536-537.
    [103] (a) Guo, Q.-L.; Dou, J.-M.; Wu, L.-B. et al. 1-Acetonitrile-3-chloro-1,2- (1-3,5-dinitrobenzoato-η2- O,O')-1-(triphenylphosphine-η-P)-closo-1-ruthenaundecaborane. Acta Crystallogr. Section E. 2005, 61:2613-2615. (b) Guo, Q.-L.; Dou, J.-M.; Wu, L.-B. et al. Synthesis and Crystal Structure of Two iso-closo 11-Vertex p-Bromobenzoate Ruthenoborane Clusters: [(PPh3)(p-BrC6H4CO2)2RuB10H8] and [(PPh3)2Ru(p-BrC6H4CO2)-(PPh3)RuB10H9]. Chin. J. Chem. 2006, 24(12):1741-1746. (c) Guo, Q.-L.; Dou, J.-M.; Wu, L.-B. et al. Synthesis and Crystal Structures of Two exo-cyclic 11-Vertex isocloso Ruthenaborane Clusters [(PPh3)(p-ClPhCO2)2RuB10H8] and [(PPh3)2Ru(PPh3)- (p-ClPhCO2) RuB10H9]·0.5C5H12·H2O . Z. Anorg. Allg. Chem. 2006, 632(9):1591-1597.
    [104] Nie, Y.; Hu, C.-H.; Sun, J. et al. An exo-polyhedral bicyclic 11-vertex closo-ruthenaborane: [(PPh3)(CH3COS)2RuB10H8]. Acta Crystallogr. Section C. 1999, 55:1224-1266.
    [105] Yao, H.-J.; Hu, C.-H.; Dou, J.-M. et al. Synthesis and molecular structure of an exo-bicyclic eleven-vertex closo-ruthenaborane [(PPh3)(C6H5COS)2RuB10H8]·(CH2Cl2). Polyhedron. 1998, 17(11-12):1877-1881.
    [106] Dou, J.-M.; Guo, Q.-L.; Wu, L.-B. et al. Synthesis, crystal structure and electrochemical properties of three isocloso eleven-vertex ferrocenecarboxylate ruthenaborane clusters. Appl. Organomet. Chem. 2006, 20(3):193-202.
    [107]李文,郑培菊,叶建萍,金属硼烷arachno-P4M2B8和closo-MB10X2分子结构的键合研究.分子科学学报,2000, 16(2):94-101.
    [108] Bown, M.; Fontaine, X. L. R.; Greenwood, N. N. et al. Organoruthenaborane chemistry. Part 7. Preparation, molecular structure, and nuclear magnetic resonance properties of eleven-vertex closo-type clusters: [2,4-Me2-1 -(pcym)-1,2,4-RuC2B8H8], [2,3-Me2-1-(pcym)-1,2,3-RuC2B8H8], [1-(pcym)-1-RuB10H10] and some related species. J. Chem. Soc. Dalton Trans. 1990, 3039-3049.
    [109] (a) Bown, M.; Fontaine, X. L. R.; Greenwood, N. N. et al. A double cluster of ruthenium and boron: [1-η2-{(η6-C6Me6)2Ru2H4}-isocloso-1-RuB10H8-2,3-(OEt)2]. J. Chem. Soc. Chem. Commun. 1987, (6):442-443.(b) Bown, M.; Fontaine, X. L. R.; Greenwood, N. N. et al. Organoruthenaborane chemistry. Part 5. Products of the reaction between closo-[B10H10]2– and [(η6-C6Me6)ClRuB3H8]. Nuclear magnetic resonance studies and the crystal and molecular structure of [{(η6-C6Me6)2Ru2H4}RuB10H8 (OEt)2]. J. Chem. Soc. Dalton Trans. 1987, 2781-2787.
    [110] Bown, M; Waters, J. M.; Fontaine, X. L. R. et al. Products of the reaction between [{(η6-C6Me6)2Ru2H4}RuB10H8(OEt)2] and carbon monoxide. Nuclear magnetic resonance studies and the crystal structure of [{(η6-C6Me6)2Ru2H2(CO)2}RuB10H8(OEt)2]. J. Organomet. Chem. 1990, 390(3):379-387.
    [111] Bown, M; Waters, J. M. Dichloromethane: a bridging ligand. J. Am. Chem. Soc. 1990, 112(6):2442-2443.
    [112] (a) Bown, M.; Greenwood, N. N.; Kennedy, J. D. Hexamethylbenzene-ruthenaborane and -osmaborane chemistry. J. Organomet. Chem. 1986, 309(3):C67- C69. (b) Bown, M.; Fontaine, X. L. R.; Greenwood, N. N. et al. Organoruthenaborane chemistry. Part 6. The reaction of [{Ru(η6-C6Me6)Cl2}2] with the closo-[B10H10]2– anion: characterisation of some closo-type eleven-vertex 1-ruthenaundecaboranes and the molecular structure of [5-(-η6- C6Me6)-6-(OMe)-nido-5-RuB9H12]. J. Chem. Soc. Dalton. Trans. 1988, 925-930.
    [113] (a)姚海军,胡春华,孙杰等.二个降解的十顶钌硼烷二元醇衍生物的合成和结构研究.化学世界,1998, 2:110-111. (b) Yao, H.-J.; Hu, C.-H.; Dou, J.-M. et al. A degraded glycol-substituted iso-closo ten-vertex ruthenaborane: [(PPh3)HClRuB9H5(OCH2CH2OH)2(PPh3)2].1.2CHCl3. Acta Crystallogr. Section C. 1999, 55:337-339.
    [114] Paxson, T. E.; Hawthorne, M. F. Nido-Metalloboranes derived from decahydrodecaborate(2-) ion. Inorg. Chem. 1975, 14(7):1604-1607.
    [115] Dou, J.-M.; Wu, L.-B.; Guo, Q.-L. et al. Synthesis and crystal structure of three nido 11-vertex platinaborane clusters. Appl. Organomet. Chem. 2005, 19(11):1168-1175.
    [116] Nie, Y.; Hu, C.-H.; Li, X. et al. Three monoalkoxy-substituted nido-platinaboranes: [(PPh3)2PtB10H11-8-(OCH3)], [(PPh3)2PtB10H11-8-{OCH(CH3)2}] and [(PPh3)2PtB10H10-9- {OCH(CH3)2}]. Acta Crystallogr. Section C. 2001, 57:897-899.
    [117] (a) Yong, W.; Hu, C.-H.; Dou, J.-M. et al. Two New Dialkoxy-substituted Nido-platinaundceaboranes:(PPh3)2PtB10H10-8,10-2(OCH2CH3)·CH2Cl2(I){(PPh3)2PtB10H10-8,10-2 [OCH(CH3)2]}(II). Chin. J. Chem. 2001, 19:1162-1164. (b)窦建民,武立斌,郭庆良等.巢式十一顶铂硼烷簇合物的合成与晶体结构.化学学报,2005, 63(12):1087-1094.
    [118] Hu, C.-H.; Yong, W.; Dou, J.-M. et al. [(P_((2)) Ph_3)Pt_((1)) (μ_2-B_ ((11))-(B_((9))-OC(CH_3)_3-B_(10) H_(10))Pt_((7))(P_ ((1))Ph_3)]_2. Chin. J. Chem. 2002, 20:536.
    [119] (a) Hu, C.-H.; Dou, J.-M.; Sun, J. et al. Exopolyhedral Cyclized Platinaundecaboranes: [(PPh3)(PhCOS)PtB10H11]·0.5CH2Cl2. Acta Crystallogr. Section C. 1998, 54:1089-1091. (b) Hu, C.-H.; Dou, J.-M.; Yao, H.-J. et al. An Exopolyhedral Cyclized Platinaundecaborane: [(PPh3)(PhCOS)PtB10H9(PPh3)]·1.5CHCl3. Acta Crystallogr. Section C. 1998, 54, 1835-1837.
    [120] (a) Dou, J.-M.; Hu, C.-H.; Yao, H.-J. et al. A Cycloboronated Nickelaundecaborane: [(PhCOS)2NiB10H8(PPh3)]. Acta. Cryst. 1997, C53:693-695. (b)Hu, C.-H.; Dou, J.-M.; Yao, H.-J. et al. ortho-Cycloboronation of a Thiobenzoate Cluster:[(PPh3)(PhCOS)2NiB10H10]·0.5C6H14. Acta Crystallogr. Section C. 1997, 53:695-697. (c) Dou, J.-M.; Hu, C.-H.; Sun, J. et al. Synthesis and crystal structure of the first metallaborane cluster containing three rings of exo-polyhedral cyclization. Polyhedron. 1997, 16(21):3873-3875. (d)窦建民,胡春华,姚海军等.簇外环化镍十硼烷簇合物的合成与结构研究.化学学报,2000, 58(7), 884-889.
    [121] (a) Dou, J.-M.; Hu, C.-H.; Yao, H.-J. et al. Synthesis and crystal structure of [(PPh3)- (CH3COS)2NiB10H10]·0.4(C5H12). Chin. J. Struct. Chem. 1999, 18(5):326-330. (b) Dou, J.-M.; Hu, C.-H.; Yao, H.-J. et al. A three-ring exo-polyhedral-cyclized nickel- aundecaborane cluster: [(CH3COS)3NiB10H7(PPh3)]. Acta Crystallogr. Section C. 1999, 55:1226-1228.
    [122] Fowkes, H.; Greenwood, N. N.; Kennedy, J. D. et al. Eleven-vertex isocloso Type Rhodaundecaboranes: Crystal Structures and Nuclear Magnetic Resonance Properties of [(PMe2Ph)2RhHB10H8(OMe)2]and [(PMe2Ph)2RhHB10H8Cl(OMe)]. J. Chem. Soc., Dalton Trans. 1986, 517-532.
    [123] Fontaine, X. L. R.; Fowkes, H.; Greenwood, N. N. et al. Pentamethylcyclopentadienylrhoda- borane Chemistry. Part 3. The Reaction of [{Rh(η5-C5Me5)Cl2}2] with closo-[B10H10]2- and arachno-B10H12-6,9(PMePh)2, and the Characterisation of Some Novel Rhodaboranes by X-Ray Diffraction Analysis and Nuclear Magnetic Resonance Spectroscopy. J. Chem. Soc., Dalton Trans. 1987, 2417-2429.
    [124] (a) Dou, J.-M.; Hu, C.-H.; Li, W. et al. A structurally characterized ortho-cycloboronated closo twelve-vertex 1,2-dinickeladodecaborane. Polyhedron. 1997, 16(13):2323-2324. (b)窦建民,胡春华,姚海军等.闭式十二顶双镍十硼烷簇合物[(μ-Cl)(Ph2PC6H4)2Ni2B(10)H6Cl(PPh3)]的合成与结构.化学学报,2002, 60(11):1993-1998. (c)窦建民,胡春华,姚海军等.两个具有混合卤素桥的闭式十二顶双镍十硼烷簇合物的合成与结构.化学学报,2003, 61(7):1006-1013.
    [125] (a) Dou, J.-M.; Hu, C.-H.; Gu, J.-M. et al. A closo-12-Vertex Dinickelaborane: [(η5-C5H5)2Ni2B10H10]. Acta Crystallogr. Section C. 1998, 54(10):1418-1419. (b) Leyden, R. N.; Sullivan, B. P.; Baker, R. T. et al. Synthesis of closo- and nido-metalloboranes from metallocenes. J. Am. Chem. Soc. 1978, 100(12):3758-3765.
    [126] Yao, H.-J.; Hu, C.-H.; Sun, J. et al. Isolation and Structure of [(PPh3)3(PPh2)2Pd4B20H16]. A Possible Prognostic for New Globular Borane-based Cluster Architectures. Collect. Czech. Chem. Comm. 1999, 64(6):927-937.
    [127] Bould, J.; Teat, S. J.; Kennedy, J. D. Polyhedral Dipallaborane Chemistry. The Molecular Structure and Cluster Electron Count of [7,8-(PPh3)2-7,8-(μ-PPh2)-9,11-(OEt)2-nido-7,8- Pd2B9H8]. Collect. Czech. Chem. Commun. 2007, 72(12):1631-1638.
    [128] (a) Dou, J.-M.; Wu, L.-B.; Guo, Q.-L. et al. A New Strategy for the Preparation of Metallaboranes - Solvothermal Synthesis and Structural Characterisation of Two Nido 11-vertex Diplatinaundecaborane Clusters. Eur. J. Inorg. Chem. 2005:63-65. (b) Wu, L.-B.; Dou, J.-M.; Guo, Q.-L. et al. Synthesis and crystal structure of a nido 11-vertex diplatinaundecaborane cluster [(μ-PPh2)(PPh3)2Pt2B9H7-9, 11-(OiPr)2]. Indian. J. Chem. Section A. 2006, 45(8):1840-1843.
    [129] (a) Hawthorne, M. F. The Role of Chemistry in the Development of Boron Neutron Capture Therapy of Cancer. Angew. Chem. Int. Ed. Engl. 1993, 32(7):950-984. (b) Soloway, A. H.; Tjarks, W.; Barnum, B. A. et al. The Chemistry of Neutron Capture Therapy. Chem. Rev. 1998, 98(4):1515-1562. (c) Gabel, D.; Mai, S.; Perleberg, O. The formation of boron-carbon bonds to closo-decaborate(2-) and closo-dodecaborate(2-). J. Organomet. Chem. 1999, 581(1):45-50. (d)Hawthorne, M. F.; Maderna, A. Applications of Radiolabeled Boron Clusters to the Diagnosis and Treatment of Cancer. Chem. Rev. 1999, 99(12):3421-3434. (e) Barth, R. F.; Coderre, J. A.; Vicente, M. G. H. et al. Boron Neutron Capture Therapy of Cancer: Current Status and Future Prospects. Clin. Cancer Res. 2005, 11(11):3987-4002. (f) Backer, M. V.; Gaynutdinov, T. I.; Patel, V. et al. Vascular endothelial growth factor selectively targets boronated dendrimers to tumor vasculature. Mol. Cancer Ther. 2005, 4:1423-1429. (g) Wu, G.; Barth, R. F.; Yang, W.-L. et a
    l. Boron Containing Macromolecules and Nanovehicles as Delivery Agents for Neutron Capture Therapy. Anti-Cancer Agents Med. Chem. 2006, 6(3):167-184.(h) Wilbur, D. S.; Chyan, M. K.; Hamlin, D. K. et al. Reagents for Astatination of Biomolecules. 2. Conjugation of Anionic Boron Cage Pendant Groups to a Protein Provides a Method for Direct Labeling that is Stable to in Vivo Deastatination. Bioconjugate Chem. 2007, 18(4):1226-1240.
    [130] (a) Heber, E.; Trivillin, V. A.; Niqq, D. et al. Biodistribution of GB-10 (Na210B10H10) compound for boron neutron capture therapy (BNCT) in an experimental model of oral cancer in the hamster cheek pouch. Arch. Oral. Biol. 2004, 49(4):313-324. (b) Diaz, A.; Stelzer, K.; Laramore, G. et al. In Research and Development in Neutron Capture Therapy. Eds., Monduzzi Editore, Bologna, 2002, 993.
    [131] Shelly, K.; Feakes, D. A.; Hawthorne, M. F. et al. Model Studies Directed Toward the Boron Neutron Capture Therapy of Cancer: Boron Delivery to Murine Tumors with Liposomes. Proc. Natl. Acad. Sci. 1992, 89(19):9039-9043.
    [132]吕一辛,丁宏勋,吕慧梅,硼中子俘获治疗肿瘤的研究I.合成硼化核酸的几种化学方法.化学学报,1990, 48(8):820-824.
    [133] Tjarks, W. The use of boron clusters in the rational design of boronated nucleosides for neutron capture therapy of cancer. J. Organomet. Chem. 2000, 614:37-47.
    [134] Bregadze, V. I.; Sivaev, I. B.; Glazun, S. A. Polyhedral Boron Compounds as Potential Diagnostic and Therapeutic Antitumor Agents. Anti-Cancer Agents Med. Chem. 2006, 6(2):75-109.
    [135] (a) Naoufal, D; Grüner, B; Stibr, B. et al. Solvent extraction of radioactive Cs+ by hydroborate anionic extractants of the [1-LB10H9]- type (L = amine or phosphine). J. Radioanal. Nuclear Chem. 2005, 266(1):145-148. (b) Naoufal, D.; Bonnetot, B.; Mongeot, H. et al. Synthesis of Bis(diphenylphosphinio)octahydro-closo-decaborates L2B10H8 (L = Ph2PH) and 1-(Diphenylphosphinio)nonahydro-closo- decaborates(1-) [1-LB10H9]- (L = Ph2PH, Ph2P(OH)) by the Palladium-Catalyzed Reaction of Ph2PH with 1-Diazononahydro-closo-decaborate(1-) [1-N2B10H9]-. Collect. Czech. Chem. Commun. 1999, 64(5):856-864.
    [136] Bernard, R.; Cornu, D.; Grüner, B. et al. Synthesis of [B12H12]2? based extractants and their application for the treatment of nuclear wastes. J. Organomet. Chem. 2002, 657(1):83-90.
    [137] Hawthorne, M. F. Cluster Catalysis with Metallacarboranes. Mol. Struct. Energ. 1988, 5:225-233.
    [138] (a) Pakhomov, S.; Kaszynski, P.; Young Jr, V. G. 10-Vertex closo-Boranes as PotentialπLinkers for Electronic Materials. Inorg. Chem. 2000, 39(10):2243-2245. (b) Miniewicz, A.; Samoc, A.; Samoc, M. et al. Observation of second-harmonic generation inan oriented glassy nematic phase of a closo-decaborane derivative. Appl. Phys. 2007, 102(3):33108. (c) Kaszynski, P.; Douglass, A. G. Organic derivatives of closo-boranes: a new class of liquid crystal materials. J. Organomet. Chem. 1999, 581(1):28-38.
    [139] White, J. P.; Shore, S. G. Complexes of divalent lanthanides (ytterbium(II), europium(II), and samarium(II)) with decaborates. Inorg. Chem. 1992, 31(13):2756-2761.
    [140] Itoh, H.; Tsuzuki, Y.; Naka, S. Synthesis of cerium and gadolinium borides using boron cage compounds as a boron source. Mater. Res. Bull. 1987, 22(9):1259-1266.
    [141] Panda, M. Synthesis and characterization of alkali metal borides and closo-hydroborates: [Ph. D. Dissertation]. Germany: Univ. Hamburg, 2006.
    [142] (a) Schouwink, P.; Berlepsch, H.; Dahne, L. et al. Dependence of Rabi-splitting on the spatial position of the optically active layer in organic microcavities in the strong coupling regime. Chem. Phys. 2002, 285(1):113-120. (b) Volkov, V. V.; Il’inchik, E. A.; Yuryeva, O. P. The Luminescence of Cluster Derivatives of Boron Hydrides, and Some Applied Aspects. Chem. Sustain. Develop. 2000, 8(1-2):185. (c) Gerasimova, T. N.; Orlova, N. A.; Shelkovnikov, V. V. et al. The structure of pseudoisocyanine decahydro-closo-decaborate and its nonlinear optical properties in thin films . Chem. Sustain. Develop. 2000, 8:109-114.
    [143] Lemmon, J. P. US 2004002577, 2004.
    [144] Kubas, G. J. Fundamentals of H2 Binding and Reactivity on Transition Metals Underlying Hydrogenase Function and H2 Production and Storage. Chem. Rev. 2007, 107(10):4152-4205.
    [145] Custelcean, R.; Jackson, J. E. Dihydrogen Bonding: Structures, Energetics, and Dynamics. Chem. Rev. 2001, 101(7):1963-1980.
    [146] Shubina, E. S.; Bakhmutova, E. V.; Filin, A. M. et al. Dihydrogen bonding of decahydro-closo-decaborate(2?) and dodecahydro-closo-dodecaborate(2?) anions with proton donors: experimental and theoretical investigation. J. Organomet. Chem. 2002, 657(2):155-162.
    [147] (a) Yang, X.-G.; Knobler, C. B.; Hawthorne, M. F. Supramolecular chemistry: molecular aggregates of closo-B10H102- with [12]mercuracarborand-4. J. Am. Chem. Soc.1993, 115(11):4904-4905. (b) Yang, X.-G.; Knobler, C. B.; Zheng, Z. et al. Host-Guest Chemistry of a New Class of Macrocyclic Multidentate Lewis Acids Comprised of Carborane-Supported Electrophilic Mercury Centers. J. Am. Chem. Soc. 1994, 116(16):7142-7159. (c) Zheng, Z.-P.; Knobler, C. B.; Mortimer, M. D. et al. Hydrocarbon-SolubleMercuracarborands: Syntheses, Halide Complexes, and Supramolecular Chemistry. Inorg. Chem. 1996, 35(5):1235-1243.
    [148] Shubina, E. S.; Tikhcojoa, I. A.; Bakhmutova, E. V. et al. Crown Compounds for Anions: Sandwich and Half-Sandwich Complexes of Cyclic Trimeric Perfluoro-o-phenylenemercury with Polyhedral closo-[B10H10]2- and closo-[B12H12]2- Anions. Chem. Eur. J. 2001, 7(17):3783-3790.
    [149] Klanberg, F.; Wegner, P. A.; Parshall, G. W. et al. Metalloboranes. II. Transition metal complexes of B10H122-. Inorg. Chem. 1968, 7(10):2072-2077.
    [150] Boocock, S, K,; Greenwood, N. N.; Kennedy, J. D. et al. The chemistry of isomers of icosaborane (26), B20H26: synthesis and nuclear magnetic resonance study of various isomers of platinahenico- saboranes and diplatinadocosaboranes, and the X-ray crystal and molecular structures of 7,7-bis- (di-methylphenylphosphine)-nido-7-platinaundecaborane and 4-(2’-nido-decaboranyl)-7,7- bis(dimethyl phenylphosphine)-nido-7-platinaundecaborane. J. Chem. Soc. Dalton Trans. 1981, 2573-2584.
    [151] Crook, J. E.; Greenwood, N. N.; Kennedy, J. D. et al. The reactions of arachno-decaboranyl complexes L2B10H12 (L = two-electron donor ligand) with some platinum(II) compounds; nuclear magnetic resonance studies and the crystal and molecular structure of [8-Cl-7,7-(PMe2Ph)2-nido -7-PtB10H11]. J. Chem. Soc. Dalton Trans. 1984, 2487-2495.
    [152] Beckett, M. A.; Greenwood, N. N.; Kennedy, J. D. et al. Preparation, crystal and molecular structure of, and NMR parameters for, the exopolyhedral heterocyclic platinaundecaborane [μ-2,7-(SCSNEt2) -7-(PMe2Ph)-NIDO-7-PtB10H11]. Polyhedron. 1985, 4(3):505-511.
    [153] Gaft, Yu. L.; Ustynyuk, Yu. A.; Borisenko, A. A.et al. Synthesis and structure of isomers of the metalloborane complex cis-[Pt(PPh3)2B10H10]. Zh. Neorg. Khim. 1983, 28(9):2234-2239.
    [154] Bailar, J. C.; Itatani, H. Hydridochlorobis(triphenylphosphine) platinum (II) and Some Related Compounds. Inorg. chem. 1965, 4(11), 1618-1620.
    [155] Paavola, S.; Teixidor, F.; Vinas, C. et al. Pd(II) bromide complexes of 1,2-bis(diphenylphosphino)-1,2-dicarba-closo-dodecaborane. Crystal structures of [PdBr2(1,2- (PPh2)2-1,2-C2B10H10)]·CH2Cl2, [PdBr1.133Cl0.867(1,2-(PPh2)2-1,2-C2B10H10)]·CH2Cl2 and [PdBrCl0.541Me0.459(1,2-(PPh2)2-1,2- C2B10H10)]·CHCl3. J. Organomet. Chem. 2002, 657(2):187–193.
    [156] Krause, U.; Preetz, W. Darstellung und spektroskopische Charaketerisierung von Carboxylatododecaboraten. Z. Anorg. Allg. Chem. 1995, 621:516-524.
    [157] Mingos, D. M. P. Molecular-orbital studies on carbametalladaboranes. Part 1. Icosahedral carbaplatinaborane polyhedra. J. Chem. Soc., Dalton Trans. 1977, (6):602-610.
    [158] Bender, R.; Braunstein, P.; Dedieu, A. et al. Synthetic, Structural, Spectroscopic, and Theoretical Studies of Structural Isomers of the Cluster Pt3(μ-PPh2)3Ph(PPh3)2. A Unique Example of Core Isomerism in Phosphine Phosphido-Rich Clusters. Inorg.Chem. 1996, 35(5):1223-1234.
    [159] Greenwood, N. N. METALLOBORANES 1983. Pure & Appl. Chem. 1983, 55(9):1415-1430.
    [160] Siedle, A. R.; Todd, L. J. Chemistry of metalloborane derivatives containing the decaborane(12) ligand. Inorg. Chem. 1976, 15(11):2838-2842.
    [161] Elrington, M.; Greenwood, N. N.; Kennedy, J. D. Homo- and hetero-bimetallic B-frame compounds: some novel twelve-vertex Ru/Ru, Os/Os, and Os/Ru metallaboranes. J. Chem. Soc. Chem. Commun. 1984, 1389-1399.
    [162] Bould, J.; Bath, R. N.; Barton, L. et al. Metallaborane Heteroatom Incorporation Reactions: Enyne Insertion into arachno-[(CO)(PMe3)2HIrB8H12] Organometallics, 1998, 17(5):902-907.
    [163]聂永.十一顶闭式钌硼烷簇合物的合成与结构研究[硕士学位论文].上海:复旦大学,1999.
    [164] Hallman, P. S.; Stephenson, T. A.; Wilkinson, G. Dichlorotris(triphenylphine)ruthenium(II). Inorg. Synth. 1970, 9:16.
    [165] Elrington, M.; Greenwood, N. N.; Kennedy, J. D. et al. Ruthenium(II) Complexes of closo-Dodecaboranyl Anions and the Molecular Structure of the pileo Thirteen-vertex Ruthenaborane [(PPh3)2ClRuB12H11(NEt3)], J. Chem. Soc., Dalton Trans. 1987, 451-456.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700