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脱水四环素的金属配合物。1. 铜(II)和镍(II)配合物的光谱研究。

Metal complexes of anhydrotetracycline. 1. A spectrometric study of the Cu(II) and Ni(II) complexes.

作者信息

de Siqueira J M, Carvalho S, Paniago E B, Tosi L, Beraldo H

机构信息

Departamento de Química, Universidade Federal de Minas Gerais, Cidade Universitária, Belo Horizonte, Brazil.

出版信息

J Pharm Sci. 1994 Mar;83(3):291-5. doi: 10.1002/jps.2600830306.

Abstract

Anhydrotetracycline (AHTC), one of the major toxic decomposition products of the antibiotic tetracycline, contains several potential binding sites to metal ions. The acidity constants of the ligand were calculated in aqueous medium (I = 0.1 M) at 25 and 37 degrees C. We found pKa1 = 3.23 +/- 0.08, pKa2 = 5.94 +/- 0.09, and pKa3 = 8.48 +/- 0.02 at 25 degrees C and pKa1 = 3.12 +/- 0.09, pKa2 = 5.86 +/- 0.03, and pKa3 = 8.38 +/- 0.04 at 37 degrees C. The coordination of AHTC to Cu(II) and Ni(II) ions was studied in the solid state as well as in buffered aqueous solution at pH 10.0. At this pH, the formation of the two CuL2 and CuL species was indicated (log beta 1 = 8.41 +/- 0.04 and log beta 2 = 12.55 +/- 0.05), but only the formation of the NiL complex (log beta = 5.74 +/- 0.04) was identified. Spectroscopic data confirm the previous assignment of the C11 and C12 oxygens as the coordination sites, yielding six-membered ring chelates and excluding complexation through any of the potential binding positions on ring A.

摘要

脱水四环素(AHTC)是抗生素四环素的主要有毒分解产物之一,含有几个与金属离子的潜在结合位点。在25℃和37℃的水介质(I = 0.1 M)中计算了该配体的酸度常数。我们发现在25℃时pKa1 = 3.23±0.08,pKa2 = 5.94±0.09,pKa3 = 8.48±0.02;在37℃时pKa1 = 3.12±0.09,pKa2 = 5.86±0.03,pKa3 = 8.38±0.04。在固态以及pH为10.0的缓冲水溶液中研究了AHTC与Cu(II)和Ni(II)离子的配位情况。在此pH值下,表明形成了两种CuL2和CuL物种(logβ1 = 8.41±0.04和logβ2 = 12.55±0.05),但仅鉴定出NiL配合物的形成(logβ = 5.74±0.04)。光谱数据证实了先前将C11和C12氧作为配位点的归属,生成了六元环螯合物,并排除了通过环A上任何潜在结合位置的络合作用。

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