structural, spectroscopic properties and biological relevance
Author: Yuan-Fu Deng Ya-Qi Jiang, Qi-Ming Hong, Zhao-Hui Zhou
Abstract
Titanium(IV) citrate complexes with different anions Na3[Ti(H2cit)2(Hcit)] · 9H2O (1), K4[Ti(H2cit)(Hcit)2] · 4H2O (2), K5[Ti(Hcit)3] · 4H2O (3) and Na7[TiH(cit)3] · 18H2O (4) (H4cit = citric acid) were isolated in pure forms from the solutions of titanate and citrate at various pH values. X-ray structural analyses revealed the presence of a monomeric tricitrato titanium unit in the four complexes. Each Ti(IV) ion is coordinated octahedrally by the three citrate ligands in different protonated forms. The citrate ligand chelates bidentately to the titanium ion through its negatively charged greek small letter alpha-alkoxy and greek small letter alpha-carboxy groups. This is consistent with the large downfield 13C NMR shifts for the carbon atoms bearing the greek small letter alpha-alkoxy and greek small letter alpha-carboxy groups. The very strong hydrogen-bonds existing in the protonated and deprotonated β-carboxy groups may be the key factor for the stabilization of the titanium citrate complexes. When the pH value is lower than 7.0, 13C NMR spectra of 1:3 Ti:citrate solutions are similar to those of the titanium citrate complexes isolated at the corresponding pH values. The dissociation of free citrate increases with the rise of pH value. However, 13C NMR spectra of 1:3 Ti:citrate solutions indicate that there may exist different citrate titanium species when the pH value is higher than 7.0.
这篇文章是关于柠檬酸钛配合物的总结,主要是报道前面还没有报道的柠檬酸钛物种。通过对柠檬酸钛化学在不同pH值的系统研究,得出了柠檬酸钛阴离子在不同pH下表现出不同的电荷状态。
Speciation of water-soluble titanium citrate.pdf
(2008-07-05 09:49:09,
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