LIQUID-CRYSTALLINE COMPOUNDS IN THE THIOPHENE SERIES .13. SYNTHESIS AND CHARACTERIZATION OF OLIGOMERIC LIQUID-CRYSTALLINE MODEL COMPOUNDS WITH VINYLENE UNITS, THIOPHENE RING-SYSTEMS AND HEXAMETHYLENE CHAINS
G. Kossmehl et Fd. Hoppe, LIQUID-CRYSTALLINE COMPOUNDS IN THE THIOPHENE SERIES .13. SYNTHESIS AND CHARACTERIZATION OF OLIGOMERIC LIQUID-CRYSTALLINE MODEL COMPOUNDS WITH VINYLENE UNITS, THIOPHENE RING-SYSTEMS AND HEXAMETHYLENE CHAINS, Liquid crystals, 22(2), 1997, pp. 137-144
'Oligomeric compounds' with three, four or six mesogenic groups in the
chain were synthesized by the Wittig reaction from different bis Witt
ig salts and various heteroaromatic aldehydes. The mesogenic,groups ar
e connected via hexamethylene moieties. All derivatives containing at
each terminal position of the chain E-1,2-di-(2-thienyl)ethylene units
and one, two or four E,E-2,5-bis(2-thienylvinyl)thiophene units in th
e chain show nematic phases while heating and/or cooling the samples (
2a, 4 and 5). Moreover, the oligomeric compound having the chain from
2a and one terminal formyl group (5) also has a nematic phase. The der
ivative with four E-2-(2-thienylvinyl)thiophene units in the chain (3a
) melts without forming a mesophase. Also two 'oligomeric compounds' w
ith benzene and thiophene systems in the mesogenic groups were synthes
ized. The compounds l)-2-thienyl]hexamethylene}-2-thienylvinyl]benzene
(2b) with three mesogenic groups and hienyl]hexamethylene}-2-thienylv
inyl]phenyl}hexane (3b) with four mesogenic groups in the chain do not
show liquid crystalline phases.