Phase characterization of LC (meth)acrylic monomers based on omega-hexyloxy- and omega-undecyloxy-salicylaldimine groups with different alkoxy tail substitutions

Soto-Bustamante, EA; Gonzalez-Henriquez, CM; Rodriguez-Lehyt, GA; Vergara-Toloza, RO

Abstract

The synthesis and phase characterization of three homologous series of liquid crystalline acrylic and methacrylic monomers, consisting of 21 new compounds are presented. They are based on ?-hexyloxy- and ?-undecyloxysalicylaldimine groups with different alkoxy tail substitutions. The liquid crystalline materials were characterized by polarizing optical microscopy and differential thermal analysis. Smectic A and tilted smectic C phases were observed in the compounds. Near the transition to the isotropic, a narrow nematic phase, coexisting with the smectic A phase, was detected for the pentyloxy and hexyloxy derivatives in the M11 and A11 series. In case of M11R11 and M11R12 only a tilted smectic C phase was detected. The clearing point was comparable for all series, around 100°C.

Más información

Título según WOS: Phase characterization of LC (meth)acrylic monomers based on omega-hexyloxy- and omega-undecyloxy-salicylaldimine groups with different alkoxy tail substitutions
Título según SCOPUS: Phase characterization of LC (meth)acrylic monomers based on ?-hexyloxy- and ?-undecyloxy-salicylaldimine groups with different alkoxy tail substitutions
Título de la Revista: LIQUID CRYSTALS
Volumen: 31
Número: 8
Editorial: TAYLOR & FRANCIS LTD
Fecha de publicación: 2004
Página de inicio: 1115
Página final: 1121
Idioma: English
DOI:

10.1080/02678290410001720173

Notas: ISI, SCOPUS