首页> 外文OA文献 >trans-Cyano(6-methyl-1,4,8,11-tetraazacyclotetradecan-6-amine)cobalt(III) bis(perchlorate) hydrate and trans-hydroxo(6-methyl-1,4,8,11-tetraazacyclotetradecan-6-amine)cobalt(III) bis(perchlorate)
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trans-Cyano(6-methyl-1,4,8,11-tetraazacyclotetradecan-6-amine)cobalt(III) bis(perchlorate) hydrate and trans-hydroxo(6-methyl-1,4,8,11-tetraazacyclotetradecan-6-amine)cobalt(III) bis(perchlorate)

机译:反式(6-甲基-1,4,8,11-四氮杂环十四烷-6-胺)钴(III)双(高氯酸盐)水合物和反式羟基(6-甲基-1,4,8,11-四氮杂环十四烷- 6-胺)钴(III)双(高氯酸盐)

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摘要

The crystal structures of a pair of closely related macrocyclic cyano- and hydroxopentaaminecobalt(III) complexes, as their perchlorate salts, are reported. Although the two complexes, [Co(CN)(C11H27N5)](ClO4)2.H2O and [Co(OH)(C11H27N5)](ClO4)(2), exhibit similar conformations, significant differences in the Co-N bond lengths arise from the influence of the sixth ligand (cyano as opposed to hydroxo). The ensuing hydrogen-bonding patterns are also distinctly different. Disorder in the perchlorate anions was clearly resolved and this was rationalized on the basis of distinct hydrogen-bonding motifs involving the anion O atoms and the N-H and O-H donors.
机译:报道了一对紧密相关的大环氰基和羟基戊胺(III)配合物的晶体结构,即它们的高氯酸盐。尽管[Co(CN)(C11H27N5)](ClO4)2.H2O和[Co(OH)(C11H27N5)](ClO4)(2)这两种络合物显示相似的构型,但Co-N键长存在显着差异产生于第六种配体的影响(氰基与羟基相反)。随之而来的氢键模式也明显不同。高氯酸根阴离子的紊乱得到了明显解决,这是基于涉及阴离子O原子以及N-H和O-H供体的独特氢键基序而合理化的。

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