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Supramolecular Tilt Chirality Derived from Symmetrical Benzene Molecules: Handedness of the 2 1 Helical Assembly
Author(s) -
Tanaka Akira,
Hisaki Ichiro,
Tohnai Norimitsu,
Miyata Mikiji
Publication year - 2007
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.200600332
Subject(s) - cholic acid , supramolecular chemistry , chirality (physics) , molecule , benzene , supramolecular chirality , crystallography , chemistry , tilt (camera) , stereochemistry , materials science , crystal structure , geometry , organic chemistry , physics , biochemistry , bile acid , nambu–jona lasinio model , chiral symmetry breaking , quantum mechanics , mathematics , quark
Achiral molecules can form aggregates with chirality. This depends on the relative position of the molecules, in other words, the tilt of the molecules (so‐called supramolecular tilt chirality). In this paper, we describe supramolecular chirality appearing in a 2 1 column composed of symmetrical benzene molecules, which is formed in the host cavity of inclusion crystals of cholic acid. Moreover, we determined the handedness, that is, right or left, of the 2 1 helical column of benzene on the basis of the molecular tilt. Determination of the 2 1 helical handedness was performed on assemblies of other benzene derivatives in cholic acid crystals and benzene assemblies in other host frameworks selected from the Cambridge Structural Database. Finally, we demonstrated complementarity of the handedness between the 2 1 symmetrical host framework of cholic acid and the benzene column.