Designed self-assembly of a bimolecular calix[4]resorcinarene capsule held together by hydrogen bonds

被引:11
|
作者
Becker, R
Reck, G
Radeglia, R
Springer, A
Schulz, B
机构
[1] Fed Inst Mat Res & Testing, BAM, D-12205 Berlin, Germany
[2] Humboldt Univ, Dept Chem, D-12489 Berlin, Germany
关键词
calix[4]resorcinarenes; hydrogen bonded molecular capsule; crystal structure; conformational chirality;
D O I
10.1016/j.molstruc.2005.08.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The X-ray crystallographic study of the macrocyclic tetrakis-N[N-2-hydroxyethyl-piperazino]calix[4]resorcinarene-3CH(3)CH(2)OH(.)H(2)O (3) reveals a self-assembled dimeric capsule-like complex held together by an array of intermolecular hydrogen bonds. Pairs of concave molecules associate directly in bowl-to-bowl fashion and enclose an accessible supramolecular cavity of 190 angstrom(3) hosting one water and three ethanol molecules. The supramolecular arrangement displays alternating layers of facing bowls and interlocking lower rim aliphatic moieties. The helical conformation of the 2-hydroxyethyl piperazinomethyl moieties displays chirality of a bimolecular capsule frozen in the solid state. 3 crystallises in the triclinic space group P-1 with two symmetry independent molecules in the asymmetric unit. Two enantiomeric capsules form a racemic pair in the unit cell. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:157 / 161
页数:5
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