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 |
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Authors: | Fumio Toda Koichi Tanaka Thomas C. W. Mak |
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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 |
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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, =91.32(2)°,RF=0.048 for 1743 observed MoK reflections; C26H20O2·HO(CH2)4OH,a=11.881(3),b=13.009(4),c=16.689(4) Å, =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. |
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Keywords: | crystal structure hydroquinone p-terphenyl dihydroanthracene hydrogen bonding host-guest compound molecular complex adduct |
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