Effects of Anion and Bipyridyl Bridging Ligand Identity on the Co(II) Coordination Networks
详细信息    查看全文
文摘
Five new coordination polymers, {[Co(OAc)2(bpe)(H2O)]路0.5(dmf)}n (1), {[Co(bpy)2(H2O)4][Co(tfa)(bpy)2(H2O)3](tfa)3路1.5(bpy)}n (2), [Co(tfa)2(dps)4]n (3), {[Co(tfa)2(bpe)4]路H2O}n (4), and [Co(tfa)2(bpp)4]n (5) (where AcO鈥?/sup> = CH3CO2鈥?/sup>; tfa鈥?/sup> = CF3CO2鈥?/sup>; bpy = 4,4鈥?bipyridine; bpe = 1,2-bis(4-pyridyl)ethane; bpp = 1,3-bis(4-pyridyl)propane; dps = 4,4鈥?dipyridyl sulfide; dmf = N,N鈥?dimethylformamide) were synthesized by the reactions of Co(OAc)2路4H2O and Co(tfa)2路4H2O with different dipyridyl ligands and characterized by elemental analysis, IR spectra, and X-ray single-crystal diffraction. Compound 1 exhibits extended two-dimensional (2D) networks through the bridging AcO鈥?/sup> and bpe ligands. The polymeric motifs in 2鈥?b>5 are exclusively based on bipyridine-type ligands and results in 1D cationic chains in 2, similar charge-neutral double tapes in 3 and 4, and a 2D polymeric network in 5. In 2鈥?b>5, the tfa anions coordinate to the Co(II) center in a monodentate mode. An impact of the anion鈥檚 fluorination on coordination modes and supramolecular architectures is registered. Magnetic measurements reveal almost vanishing exchange interactions in the layered materials 1 and 5. The correlation of mechanical properties and crystal structure has been demonstrated for 1.

© 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