Dipartimento Di Scienze Chimiche e Farmaceutiche, Università di Trieste, 34137 Trieste, Italy.
J Inorg Biochem. 2012 Nov;116:215-27. doi: 10.1016/j.jinorgbio.2012.07.018. Epub 2012 Aug 5.
The interligand interactions in coordination compounds have been principally interpreted in terms of cis and trans influences and effects, which can be defined as the ability of a ligand X to affect the bond of another ligand, cis or trans to X, to the metal. This review analyzes these effects/influences in cobalamins (XCbl) and their simple models cobaloximes, LCo(chel)X. Important properties of these complexes, such as geometry, stability, and reactivity, can be rationalized in terms of steric and electronic factors of the ligands. Experimental evidence of normal and inverse trans influence is described in alkylcobaloximes for the first time. The study of simple B(12) models has complemented that on the more complex cobalamins, with particular emphasis on the properties of the axial L-Co-X moiety. Some of the conclusions reached for the axial fragment of simple models have also been qualitatively detected in cobalamins and have furnished new insight into the as yet unestablished mechanism for the homolytic cleavage of the Co - C bond in the AdoCbl-based enzymes.
配合物中的配体相互作用主要根据顺式和反式影响和效应来解释,这些效应可以定义为配体 X 影响与 X 处于顺式或反式位置的另一个配体与金属键的能力。这篇综述分析了钴胺素 (XCbl) 及其简单模型钴胺肟 LCo(chel)X 中的这些效应/影响。这些配合物的重要性质,如几何形状、稳定性和反应性,可以根据配体的空间和电子因素来合理化。首次在烷基钴胺肟中描述了正常和反式影响的实验证据。对简单 B(12)模型的研究补充了对更复杂的钴胺素的研究,特别强调了轴向 L-Co-X 部分的性质。在简单模型的轴向片段中得出的一些结论也在钴胺素中定性地检测到,并为尚未建立的 AdoCbl 基酶中 Co - C 键的均裂裂解机制提供了新的见解。