Synthesis and properties of biphenyl liquid crystal diluters terminated by 2,2-difluorovinyloxyl for high birefringence liquid crystals

Abstract

ABSTRACT A series of liquid crystal (LC) diluters containing a rigid biphenyl core with a lateral fluorine substituent, a 2,2-difluorovinyloxyl terminal group and a flexible n-alkyl chain were designed and synthesised through classical organic synthetic reactions. Their chemical structures were characterised and confirmed by traditional methods. Meanwhile, the effects of alkyl-chain length, terminal group and lateral fluorine substituent on the melting point (T m), birefringence (Δn), dielectric anisotropy (Δε) and rotational viscosity (γ 1) of LC diluters were investigated. Density functional theory (DFT) calculations were employed to obtain the molecular polarisability, dipole moment, frontier orbitals, biphenyl dihedral angle and aspect ratio. Furthermore, their comprehensive properties in low-Δn LC mixture 002 and high-Δn LC mixture P01-F were further evaluated, and it was found that the 2,2-difluorovinyloxyl LC diluter 3FV have a significant advantage in reducing the T m and γ 1 of LC mixtures, and increasing the values of Δn and Δε. The research results provide technical support and theoretical guidance for the molecular design of new LC diluters and the development of fast response liquid crystals.