Conserved supramolecular architecture in polymetallic nucleobase complexes

被引:8
作者
Amantia, David [1 ]
Shipman, Michelle A. [1 ]
Price, Clayton [1 ]
Elsegood, Mark R. J. [1 ]
Clegg, William [1 ]
Houlton, Andrew [1 ]
机构
[1] Newcastle Univ, Chem Labs, Sch Nat Sci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
英国工程与自然科学研究理事会;
关键词
X-ray crystal structures; metal complex; supramolecular; nucleobase;
D O I
10.1016/j.ica.2006.01.009
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The single crystal X-ray structures of two different polynuclear metal-nucleobase complexes are reported. Crystals isolated from the reaction of CdBr2 with ethylenediamine-N9-ethyladenine, A-Et-en, were characterised by X-ray structural analysis as a coordination polymer [mu-{CdBr(N3,N7-A-Et-en)}(2)CdBr4] (2). Reaction of the Pd(II)-adenine complex, [PdCl(N3-A-Et-en)](+), with sodium uracilate yielded [(Pd(N3-A-Et-en)(2)(N1,N3-U)][ClO4](2) (3). Despite the considerable differences in the nature of the compounds the crystal structures feature essentially similar supramolecular architectures. A building block analysis demonstrates how this arises and reveals an approach, based on bond-type substitution and molecular replacement, to conserving such features. This may be a useful approach that could be more widely adopted in crystal engineering strategies. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:3515 / 3520
页数:6
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