Stabilization of the non-canonical adenine-adeninium base pair by N(7) coordination of Zn(II)

被引:18
作者
Amo-Ochoa, P
Alexandre, SS
Pastor, C
Zamora, F [1 ]
机构
[1] Univ Autonoma Madrid, Fac Ciencias, Dept Quim Inorgan, E-28049 Madrid, Spain
[2] Univ Alfonso X El Sabio, Dept Tecnol Ind, Madrid 28691, Spain
[3] Univ Autonoma Madrid, Dept Fis Mat Condensada, E-28049 Madrid, Spain
[4] Univ Autonoma Madrid, Serv Interdepartmental Apoyo Invest Rayos X, E-28049 Madrid, Spain
关键词
Zn(II)-nucleobases; supramolecular assemblies; crystal structure; ab initio calculations;
D O I
10.1016/j.jinorgbio.2005.07.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new zinc (II) compound with 9-ethyladenine (9-EtA) of formula [Zn(9-EtA-N7)Cl-3](9-EtAH) has been synthesized and characterized by X-ray diffraction. Its X-structure consists of an Zn(II) anionic complex and 9-ethyladeninium as counteranion. The Zn(II) complex shows a distorted tetrahedral geometry in which three Cl and an 9-EtA coordinates through N(7) position are the ligands. An indirect chelation via intramolecular H-bond between N(6)H and an Cl ligand is present in the complex. The network of [Zn(9-EtA-N7)Cl3](9-EtAH) shows interesting features. Thus, self-association of coordinated adenine-adeninium takes place by H-bonding of N(6)-H center dot center dot center dot N(1) and N(6)-H center dot center dot center dot N(7), leading to a polymeric ribbon-like ID supramolecular arrangement. Ab initio calculations have been applied in order to study the stability of the adenine-adeninium interaction due to the coordination of the Zn(II) to the N(7) position and to compare experimental and theoretical structural data. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:2226 / 2230
页数:5
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