THE RELATIONSHIP BETWEEN MOLECULAR-STRUCTURE AND MESOMORPHIC PROPERTIES OF 2,2'-DIFLUOROTERPHENYLS AND 3,2'-DIFLUOROTERPHENYLS SYNTHESIZED BY PALLADIUM-CATALYZED CROSS-COUPLINGS

Citation
M. Hird et al., THE RELATIONSHIP BETWEEN MOLECULAR-STRUCTURE AND MESOMORPHIC PROPERTIES OF 2,2'-DIFLUOROTERPHENYLS AND 3,2'-DIFLUOROTERPHENYLS SYNTHESIZED BY PALLADIUM-CATALYZED CROSS-COUPLINGS, Liquid crystals, 18(1), 1995, pp. 1-11
Citations number
27
Categorie Soggetti
Crystallography
Journal title
ISSN journal
02678292
Volume
18
Issue
1
Year of publication
1995
Pages
1 - 11
Database
ISI
SICI code
0267-8292(1995)18:1<1:TRBMAM>2.0.ZU;2-J
Abstract
Several homologues of two structurally different types of mesogenic di fluoroterphenyls have been prepared. One set of compounds contains two inner-core fluoro-substituents and the other set possesses both an in ner-core and an outer-core fluoro-substituent. The use of various type s of palladium-catalysed cross-coupling reactions was invaluable in th e synthesis (for example, selective couplings, and couplings to triflu oromethanesulphonate derivatives). Additionally, a novel selective lit hiation is reported. The mesogenic materials are all low melting and t he types of mesophase generated are considerably structure dependent. However, most of the materials support the tilted S(C) phase which is required of ferroelectric host materials. The mesomorphic behaviour of these novel materials is discussed in terms of the molecular structur e and the structure/property relationships are compared with those for difluoroterphenyls with different arrangements of lateral fluoro-subs titution.