New Family of Enantiomerically Pure Liquid Crystals Containing a Chiral Biphenyl Core | Zendy

Solladié Guy | Zendy; Hugelé Philippe | Zendy; Bartsch Richard | Zendy; Skoulios Antoine | Zendy

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New Family of Enantiomerically Pure Liquid Crystals Containing a Chiral Biphenyl Core

Author(s) -

Solladié Guy,

Hugelé Philippe,

Bartsch Richard,

Skoulios Antoine

Publication year - 1996

Publication title -

angewandte chemie international edition in english

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 0570-0833

DOI - 10.1002/anie.199615331

Subject(s) - biphenyl , chirality (physics) , core (optical fiber) , liquid crystal , crystallography , aryl , materials science , liquid crystalline , axial chirality , stereochemistry , chemistry , enantioselective synthesis , organic chemistry , chiral symmetry , catalysis , physics , composite material , optoelectronics , alkyl , quantum mechanics , nambu–jona lasinio model , quark

Cholesteric mesophases are formed by compounds of type 1 with axial chirality. The key to this behavior is the rigid twisted biphenyl core; the planes of the two aryl rings form an angle of 56° (R R′ 4‐C 8 H 17 OC 6 H 4 CO 2 ).

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