Yelamaggad Channabasaveshwar V, Shashikala Indudhara Swamy, Hiremath Uma S, Liao Guangxun, Jakli Antal, Rao Doddamane S Shankar, Prasad Subbarao Krishna, Li Quan
Centre for Liquid Crystal Research, Jalahalli, Bangalore-560013, India.
Liquid Crystal Institute, Kent State University, Kent, Ohio 44242, USA.
Soft Matter. 2006 Aug 16;2(9):785-792. doi: 10.1039/b608278e.
The phase transitional behavior of two homologous series of five-ring banana-shaped compounds comprising fluorine substituents synthesized through covalent linking of two chemically dissimilar rod-like anisometric cores (arms) to central 1,3-phenylene is reported. The novelty of these molecules originates from the fact that the molecules are highly nonsymmetrical. One of the arms, which is either salicylaldimine or Schiff base core, possesses two vicinal fluorine atoms at the terminal ring having a -decyloxy tail; while the -alkyl tail attached to the other arm was varied to realize a homologous series of compounds. The mesophases have been characterized by several complementary studies. The banana-shaped systems having short or medium alkyl chain lengths form apolar columnar (two-dimensional) structures, while on ascending the series, a polar smectic phase is stabilized. Detailed electro-optical investigations on one of the polar smectic phases revealed a synclinic antiferroelectric (racemic) ground state structure, which switches, as expected, to an anticlinic ferroelectric state by the application of an electrical field. At higher field strengths applied for an extended time interval, the anticlinic ferroelectric state switches to a synclinic ferroelectric (chiral) state. Upon field removal, these domains switch to an anticlinic antiferroelectric (chiral) state, which eventually nucleates to the original antiferroelectric synclinic (racemic) state. Remarkably, the associated spontaneous polarization value exceeds 800 nC cm, which is among the highest reported hitherto.
