3D-supramolecular copper(I) cyanide coordination polymers through hydrogen bonding

被引:38
|
作者
Etaiw, Safaa El-din H. [1 ]
Amer, Said A. [1 ]
El-bendary, Mohamed M. [1 ]
机构
[1] Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
关键词
Copper cyanide; Supramolecular coordination polymer; Acetylpyridine; Hydrogen bonding; METAL-ORGANIC FRAMEWORKS; MIXED-VALENCE POLYMER; CRYSTAL-STRUCTURE; VIBRATIONAL SPECTROSCOPY; BUILDING-BLOCKS; PI-STACKING; MULTINUCLEAR; COMPLEXES; CHEMISTRY; ADDUCTS;
D O I
10.1016/j.poly.2009.05.028
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reactions of K-3[Cu(CN)(4)], 3-acetylpyridine (3-Acpy) or 4-acetylpyridine (4-Acpy) in the presence of Me3SnCl in H2O/acetonitrile media at room temperature afford the 3D-supramolecular coordination polymers (SCPs)(infinity)(3)[Cu2CN(mu-CN)center dot(3-Acpy)(2)] 1 and (3)(infinity)[Cu2CN(mu-CN)center dot(4-Acpy)(2)] 2. The structures of 1 and 2 consist of Cu2CN building blocks which are connected by CN groups, forming 1D-zig-zag chains. Each chain is bonded to another chain by hydrogen bonding into a 2D-layer. which is further stacked in an interwoven mode by pi-pi stacking interactions and hydrogen bonds in 1 and 2, as well as Cu center dot center dot center dot Cu interactions in 1, to create supramolecular 3D-network structures. The high dimensional topologies of 1 and 2 result mainly from extensive hydrogen bonding and pi-pi stacking. The long wavelength absorption band at 400-420 nm in the electronic spectra of 1 and 2 is assigned to a CT from copper(I) to the Acpy ligand. Compound 2 exhibits strong luminescence at 485 and 527 nm, corresponding to MLCT and metal-centered transitions, respectively. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:2385 / 2390
页数:6
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