N. Kawatsuki et al., SYNTHESIS, CHARACTERIZATION AND PHOTOREACTION OF SIDE-CHAIN LIQUID-CRYSTALLINE POLYMERS COMPRISING CINNAMOYL BIPHENYL MESOGEN, Macromolecular chemistry and physics, 197(6), 1996, pp. 1919-1935
Liquid-crystalline (meth)acrylate monomers and polymers having mesogen
ic groups based on 4-alkyloxy-4'-cinnamoylbiphenyl (m = 2, 6) were syn
thesized. The methacrylate monomers 4c, d were polymerized by free rad
ical polymerization. Under the same conditions, the acrylate monomers
4a, b gave unidentified polymers in very low yield. To synthesize the
acrylate polymer, the acrylate monomer having 4-alkyloxy-4'-hydroxybip
henyl (m = 2, 6) was polymerized followed by the esterification of the
hydroxy group using cinnamoyl chloride. All synthesized polymers havi
ng mesogenic moieties showed liquid-crystalline phases in the high tem
perature range between 140 degrees C and 245 degrees C. The difference
of aggregation of the cinnamoyl biphenyl mesogen among the polymers w
as studied by UV-VIS spectroscopy at various temperatures. The photore
action was performed in both solution and thin film. The [2+2] cycload
dition reaction preferentially occurred in the thin film although both
[2+2] cycloaddition and photo-Fries reactions could occur in the solu
tion.