Abstract
The synthesis and properties of (E)-α,β-difluorostilbene derivatives were studied. In particular, we investigated three suppression methods of (E)–(Z) isomerisation by shortening the molecular conjugation length, which included the introduction of a fluorine atom into the ortho or para position of the benzene ring or the replacement of the benzene ring with a cyclohexane ring. The relationship between the molecular structure of liquid crystals and the level of isomerisation by ultraviolet (UV) light was discussed.
Acknowledgements
We thank Mr. K. Kitajima, Mr. T. Koike and Ms. K. Isono and Ms. T. Watanabe from AGC Seimi Chemical for the physical evaluation of the new LC compounds.