结晶学
羧酸盐
化学
铜
密度泛函理论
四水合物
配体(生物化学)
氢键
分子
配位聚合物
齿合度
晶体结构
立体化学
计算化学
有机化学
生物化学
受体
作者
Fatih Şen,Sevgi Kansız,İ. Uçar
出处
期刊:
日期:2017-06-12
卷期号:73 (7): 517-524
被引量:23
标识
DOI:10.1107/s2053229617008452
摘要
Transition metal atoms can be bridged by aliphatic dicarboxylate ligands to produce chains, layers and frameworks. The reaction of copper sulfate with succinic acid (H 2 succ) and N , N- diethylethylenediamine (deed) in basic solution produces the complex catena -poly[[[( N , N -diethylethylenediamine-κ 2 N , N ′)copper(II)]-μ-succinato-κ 2 O 1 : O 4 ] tetrahydrate], {[Cu(C 4 H 4 O 4 )(C 6 H 16 N 2 )]·4H 2 O} n or {[Cu(succ)(deed)]·4H 2 O} n . Each carboxylate group of the succinate ligand coordinates to a Cu II atom in a monodentate fashion, giving rise to a square-planar coordination environment. The succinate ligands bridge the Cu II centres to form one-dimensional polymeric chains. Hydrogen bonds between the ligands and water molecules link these chains into sheets that lie in the ab plane. Density functional theory (DFT) calculations were used to support the experimental data. From these calculations, a good linear correlation was observed between the experimental and theoretically predicted structural and spectroscopic parameters ( R 2 ∼ 0.97).
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