Coordination properties of didentate N,O heterocyclic alcohols and aldehydes towards Cu(II), Co(II), Zn(II) and Cd(II) ions in the solid state and aqueous solution

被引:73
作者
Barszcz, B [1 ]
机构
[1] Jan Kochanowski Univ Humanities & Sci, Inst Chem, PL-25020 Kielce, Poland
关键词
heterocyclic alcohols; heterocyclic aldehydes; chelating ligands; metal(H) complexes; stability constants; crystal structures;
D O I
10.1016/j.ccr.2005.02.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A critical discussion of the coordination properties of some heterocyclic alcohols and aldehydes derived from imidazole, pyrazole or pyridine are the subject of this review. The versatility of these ligands, which may act as monodentate or didentate, either neutral or deprotonated, and which undergo tautomeric equilibria upon coordination to Cu(II), Zn(II), Co(II) and Cd(II) is discussed and illustrated using relevant examples. Special attention is paid to a comparison of results obtained by the X-ray diffraction method in the solid state with those acquired by the potentiometric, NMR and EPR methods in aqueous solution. A discussion of the crystal structures, as well as a correlation of the stability constants of reported complexes is also provided. Additionally, differences in the geometries of the central ions of these complexes, which extend from tetrahedral (most common for zinc) to the octahedral form for cobalt and dodecahedral for cadmium (and-copper) complexes respectively, are extensively discussed. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:2259 / 2276
页数:18
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