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Interaction of dihydroxy host systems with glycols. A comparative study of the crystal structures of 1:1 molecular complexes of 1,4-butanediol with 2,5-bis(4-chlorophenyl)hydroquinone andtrans-9,10-dihydroxy-9,10-diphenyl-9,10-dihydroanthracene
Authors:Fumio Toda  Koichi Tanaka  Thomas C. W. Mak
Affiliation:(1) Department of Industrial Chemistry, Faculty of Engineering, Ehime University, 790 Matsuyama, Japan;(2) Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong
Abstract:The title compounds crystallize in space groupC2/c withZ=4; C18H12O2Cl2·HO(CH2)4OH,a=16.186(3),b=7.626(1),c=16.939(3) Å, beta=91.32(2)°,RF=0.048 for 1743 observed MoKagr reflections; C26H20O2·HO(CH2)4OH,a=11.881(3),b=13.009(4),c=16.689(4) Å, beta=110.67(2)°,RF=0.066 for 1783 data points. Both structures feature centrosymmetric hydrogen-bonded (OH)4 rings formed by molecular components located in special positions. Different packing modes account for the observed conformations (g+ag andaaa, respectively) of 1,4-butanediol and its possible replacement by 1,2-ethanediol as a guest in the former crystal structure.Supplementary Data relating to this article are deposited with the British Library as Supplementary Publication No. SUP 82009 (25 pages).Dedicated to Professor H. M. Powell.
Keywords:crystal structure  hydroquinone  p-terphenyl  dihydroanthracene  hydrogen bonding  host-guest compound  molecular complex  adduct
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