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多核配合物在 Ca(II)和七葡萄糖酸根离子的水溶液中的形成。

Multinuclear complex formation in aqueous solutions of Ca(II) and heptagluconate ions.

机构信息

Department of Inorganic and Analytical Chemistry, University of Szeged, Dóm tér 7, Szeged, H-6720 Hungary.

出版信息

Dalton Trans. 2013 Jun 21;42(23):8460-7. doi: 10.1039/c3dt00099k. Epub 2013 Apr 30.

Abstract

The equilibria and structure of complexes formed between the Ca(2+) ion and the heptagluconate (Hglu(-)) ion in both neutral and alkaline solutions have been studied. In alkaline solutions an uncharged, multinuclear complex is formed with the composition of Ca3Hglu2(OH)4 (or Ca3Hglu2H(-4)) with an unexpectedly high stability constant (lg β(32-4) = 14.09). The formation of the trinuclear complex was deduced from potentiometry and confirmed by freezing-point depression measurements and conductometry as well. The binding sites of Hglu(-) were determined from NMR measurements. Besides the carboxylate group, the O atoms on the second and third carbon atoms proved to be the most probable sites for Ca(2+) binding.

摘要

已经研究了 Ca(2+) 离子与庚六糖酸根离子(Hglu(-))在中性和碱性溶液中形成的配合物的平衡和结构。在碱性溶液中,形成了一种不带电的多核配合物,其组成为 Ca3Hglu2(OH)4(或 [Ca3Hglu2H(-4)](0)),具有出人意料的高稳定常数(lg β(32-4) = 14.09)。通过电位法推断出三核配合物的形成,并通过冰点降低测量和电导率测量得到证实。通过 NMR 测量确定了 Hglu(-)的结合位点。除了羧酸盐基团外,第二个和第三个碳原子上的 O 原子被证明是 Ca(2+)结合的最可能位点。

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