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Synthesis and thermal properties of side‐chain liquid crystalline polyethers with racemic and chiral backbone
Author(s) -
Taton Daniel,
Borgne Alain Le,
Spassky Nicolas,
Friedrich Claude,
Noël Claudine
Publication year - 1994
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.1994.220050401
Subject(s) - liquid crystal , differential scanning calorimetry , materials science , biphenyl , epichlorohydrin , polymer , phase (matter) , side chain , monomer , polymerization , polymer chemistry , crystallography , organic chemistry , chemistry , composite material , physics , optoelectronics , thermodynamics
Racemic and chiral [(4‐cyano‐4′‐biphenyl)oxy] and [(4‐methoxy‐4′‐biphenyl)oxy]methyloxiranes were prepared from racemic epichlorohydrin or racemic and chiral glycidols and polymerized in dimethylsulfoxide (DMSO) with Bu t OK as the initiator system. Initial phase identifications were made by differential scanning calorimetry (DSC) and optical microscopy techniques and confirmed by X‐ray diffraction measurements. Upon heating, all the monomers show only a crystal–isotropic phase transition. The racemic and chiral [(4‐cyano‐4′‐biphenyl)oxy]methyloxiranes exhibit a nematic and a cholesteric monotropic phase, respectively. Methoxybiphenyl substituted polyethers are crystalline and insoluble in virtually all common solvents. Cyanobiphenyl substituted polyethers are soluble under the same experimental conditions and show enantiotropic liquid crystalline properties. The racemic polymer exhibits a nematic phase, while the optically active polymer forms a cholesteric phase.