Single- and mixed-ligand copper(ii) complexes with tris(hydroxymethyl)aminomethane and polyamines

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
N. V. Scheglova, T. V. Popova, A. S. Verbitsky
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引用次数: 0

Abstract

The reactions giving single- and mixed-ligand coordination compounds in ternary systems containing copper(ii) cations, tris(hydroxymethyl)aminomethane, and polyamines (ethylenediamine, diethylenetriamine, or triethylenetetramine) were studied in aqueous solutions by spectrophotometry. By changing the component composition of solutions of ternary systems, the optimal conditions were found for the formation of coordination species, and their composition was determined from the electronic absorption spectra. In alkaline solutions of the ternary copper(ii)—tris(hydroxymethyl)aminomethane—ethylenediamine system, the formation of a mixed-ligand complex with an equimolar composition of the coordination sphere was confirmed, for which logβ is 12.83±0.24. For the ternary copper(ii)—tris(hydroxymethyl)aminomethane—tdiethylenetriamine or triethylenetetramine systems, the preferential coordination of polyamines, in which the complexing properties of the aminohydroxyl ligand are blocked, was established.

单配体和混合配体铜(ii)与三(羟甲基)氨基甲烷和多胺配合物
用分光光度法研究了含铜(ii)阳离子、三(羟甲基)氨基甲烷和多胺(乙二胺、二乙三胺或三乙四胺)三元体系中单配体和混合配位化合物的反应。通过改变三元体系溶液的组分组成,找到了配位物质形成的最佳条件,并通过电子吸收光谱确定了配位物质的组成。在铜(ii) -三(羟甲基)氨基甲烷-乙二胺三元体系的碱性溶液中,证实了混合配体配合物的形成,其配位球组成为等摩尔,其logβ为12.83±0.24。对于铜(ii) -三(羟甲基)氨基甲烷-二乙基三胺或三乙基四胺三元体系,建立了多胺的优先配位,其中氨基羟基配体的配合性能被阻断。
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来源期刊
Russian Chemical Bulletin
Russian Chemical Bulletin 化学-化学综合
CiteScore
2.70
自引率
47.10%
发文量
257
审稿时长
3-8 weeks
期刊介绍: Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections: General and Inorganic Chemistry; Physical Chemistry; Organic Chemistry; Organometallic Chemistry; Chemistry of Natural Compounds and Bioorganic Chemistry.
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