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首页> 外文期刊>Journal of chemical crystallography >Isolation and crystal structure of [Cu(L1)(O2CH)](ClO4) center dot H2O: Hydrolysis of DMF (N,N-dimethylformamide) by a copper(II) tetraazamacrocycle
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Isolation and crystal structure of [Cu(L1)(O2CH)](ClO4) center dot H2O: Hydrolysis of DMF (N,N-dimethylformamide) by a copper(II) tetraazamacrocycle

机译:[Cu(L1)(O2CH)](ClO4)中心点H2O的分离和晶体结构:四氮杂铜(II)水解DMF(N,N-二甲基甲酰胺)

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摘要

The tetraazamacrocyclic copper(II) complex, [Cu(L)](ClO4)(2) (L = 3,14-dimethyl-2,6,13,17-tetraazatricyclo[14.4.0(1.18) center dot 0(7.12)]docosane), hydrolyzes DMF at room temperature. The formate anion which is one of the hydrolyzed species of DMF coordinates to the copper(II) ion to form [Cu(L1)(O2CH)](ClO4) center dot H2O (1). The crystals of the complex I were isolated and structurally characterized by a combination of analytical, spectroscopic, and crystallographic methods. In 1, the macrocyclic ligand contains two trans fused cyclohexane rings, and the coordination geometry about the copper(II) ion adopts a square pyramid with four equatorial nitrogen atoms from the macrocycle and an oxygen atom from the formato ligand with an uncoordinated perchlorate ion.
机译:四氮杂大环铜(II)络合物[Cu(L)](ClO4)(2)(L = 3,14-二甲基-2,6,13,17-四氮杂三环[14.4.0(1.18)中心点0(7.12) )]二十二烷),在室温下水解DMF。作为DMF水解物之一的甲酸酯阴离子与铜(II)离子配位形成[Cu(L1)(O2CH)](ClO4)中心点H2O(1)。分离出配合物I的晶体,并通过分析,光谱学和晶体学方法的组合对结构进行表征。在图1中,大环配体包含两个反式稠合的环己烷环,并且关于铜(II)离子的配位几何结构采用四角锥,其中大环上有四个赤道的氮原子,而甲酸酯配体中的氧原子带有未配位的高氯酸根离子。

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