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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

โœ Scribed by Barbara Barszcz


Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
589 KB
Volume
249
Category
Article
ISSN
0010-8545

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โœฆ Synopsis


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.


๐Ÿ“œ SIMILAR VOLUMES


Nickel(II) Complexes of Chiral Tripodal
โœ Berkessel, Albrecht ;Seidel, Lutz ;Bats, Jan W. ;Bolte, Michael ;Neumann, Thomas ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Wiley (John Wiley & Sons) ๐ŸŒ English โš– 683 KB

The complexation behavior of three chiral, tripodal N,O,Sligands with nickel(I1) salts was examined. It was found that the coordination mode of the ligands (bidentate N,O and N,S; tridentate N,O,S) and of the central nickel ion (square-planar vs. pseudo-octahedral) is not simply an intrinsic propert