SYNTHESIS AND PROPERTIES OF OPTICALLY-ACTIVE PHENOXYPROPIONATES - EFFECT OF HALOGENO SUBSTITUENT IN THE CORE ON PHYSICAL-PROPERTIES

Citation
Si. Sugita et al., SYNTHESIS AND PROPERTIES OF OPTICALLY-ACTIVE PHENOXYPROPIONATES - EFFECT OF HALOGENO SUBSTITUENT IN THE CORE ON PHYSICAL-PROPERTIES, Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals, 237, 1993, pp. 399-406
Citations number
11
Categorie Soggetti
Crystallography
ISSN journal
1058725X
Volume
237
Year of publication
1993
Pages
399 - 406
Database
ISI
SICI code
1058-725X(1993)237:<399:SAPOOP>2.0.ZU;2-0
Abstract
Chiral phenoxypropionates having halogenated 2,5-diphenylpyrimidine co res were synthesized and the effect of a halogeno-substituent on the p hysical properties such as mesomorphic behavior, spontaneous polarizat ion (Ps) and response time (tau) were investigated. The introduction o f a halogen atom to the phenyl ring of 2,5-diphenylpyrimidine core led to a decrease in the thermal stability of mesophases. The Ps values i n the achiral host liquid crystal mixture were increased by introducin g the halogen atom. However, response times were not improved.