0000000000388068
AUTHOR
S. V. Shilov
showing 3 related works from this author
Ordering and mobility of ferroelectric liquid crystal dimer as studied by FT-IR spectroscopy with 2D-IR correlation analysis
1997
Both a conservative rapid-scan FT-IR technique and a novel step-scan FT-IR technique with 2D correlation analysis were used to study the orientation and the mobility ofa ferroelectric liquid crystal dimer during switching under an electric field. The detailed mutual arrangements of different molecular segments (mesogen, poly(methylene) chain, polysiloxane chain) in a smectic C* phase were derived from the static spectra. It was shown that the long mesogen axis, the average poly(methylene) and the average polysiloxane chain axes do not coincide with each other. The hindered rotation of the carbonyl group is confirmed. Time-resolved FT-IR technique was used to follow the segmental motion with…
Fourier-transform infrared study of the switching process in a ferroelectric liquid crystalline polymer
1995
The implementation of the step-scan technique on our spectrometer enabled us to follow the electric field induced reorientation dynamics of different molecular segments of the ferroelectric liquid crystalline polymer [Si(Me)(R)O/Si(Me)(R')O/Si(Me) 2 O] n (R= (CH 2 ) 11 OPhCOOPhOCO * CHCl * CH(Me)(Et); R'= (CH 2 ) 11 OPhN=NPhO * CH(Me)(Hex)) on a sub-millisecond time scale. It was detected that not only the mesogen but also the spacer and at least part of the backbone take part in the reorientation process
Time-Resolved Fourier-Transform Infrared Spectroscopy on the Inter- and Intramolecular Orientational Dynamics in Ferroelectric Liquid Crystalline Dim…
1997
On a base of time-resolved step-scan IR-spectroscopy data, we present a detailed model of the segmental reorientation during the ferroelectric and electroclinic switching of a chiral liquid crystalline dimer. We detected that the magnitude of the motion of the molecular segments differ from each other: The tilt angle is maximal for the mesogens and minimal for the ``virtual polysiloxane backbone.'' In contrast to a recently published conjecture, we prove that in the \ensuremath{\mu}s scale the responses of different molecular segments are unambiguously synchronous with each other.