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首页> 外文期刊>Russian Chemical Bulletin >Boron cluster anions B_(10)H_(10)~(2-) and B_(10)H_(11)~- in complexation reactions of copper(I). Positional isomers of the complex [Cu2(9Nphen)4B_(10)H_(10)]
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Boron cluster anions B_(10)H_(10)~(2-) and B_(10)H_(11)~- in complexation reactions of copper(I). Positional isomers of the complex [Cu2(9Nphen)4B_(10)H_(10)]

机译:铜(I)络合反应中的硼簇阴离子B_(10)H_(10)〜(2-)和B_(10)H_(11)〜-。配合物[Cu2(9Nphen)4B_(10)H_(10)]的位置异构体

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摘要

The complexation reactions of Cu~I with the B_(10)H_(10)~(2-) anion and its protonated form, the B_(10)H_(11)~- anion, were studied in the presence of phenanthridine (9Nphen). Depending on the reaction conditions, positional isomers of the monomeric copper(I) complex [Cu2(9Nphen)4B_(10)H_(10)] were selectively isolated. The closo-decaborate anion in the complexes is coordinated to the Cu(I) atoms through the apical edges 1-2, 7(8)-10 or 1-2, 1-4 via the formation of multicenter CuHB bonds. The crystal structures and IR spectra of the complexes were studied. The compound [Cu2(9Nphen)4B_(10)H_(10)] is the first monomeric complex isolated in the form of the 1-2, 7(8)-10 isomer. It extends the series of positional isomers, which we have described earlier.
机译:在菲啶(9Nphen)存在下研究了Cu〜I与B_(10)H_(10)〜(2-)阴离子及其质子化形式B_(10)H_(11)〜-阴离子的络合反应)。根据反应条件,选择性地分离单体铜(I)配合物[Cu 2(9Nphen)4 B_(10)H_(10)]的位置异构体。通过形成多中心CuHB键,络合物中的closo-破坏型阴离子通过顶边缘1-2、7(8)-10或1-2、1-4与Cu(I)原子配位。研究了配合物的晶体结构和红外光谱。化合物[Cu2(9Nphen)4B_(10)H_(10)]是以1-2,7(8)-10异构体的形式分离的第一单体配合物。它扩展了我们先前描述的一系列位置异构体。

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