Search results for "Mesogen"

1992

A series of liquid-crystalline copolymers 1 with a chiral azobenzene moiety as photoreactive mesogenic unit was prepared. The polymers were fractionated and the mesophase behaviour of the high- and low-molecular weight fractions was examined. The copolymers display smectic A and cholesteric phases. For the cholesteric phases the pitch of the helix was determined, which ranges from 3 to 20 μm. Stable monolayers at the air-water interface were obtained from two monomers and one of the homopolymers. Multilayer assemblies of the azobenzene-containing polymers can be used to study photo-induced order/disorder transitions.

1994

Liquid crystalline side chain polymers containing photoreactive azobenzene chromophores in the dark-adapted trans form and phenylbenzoate groups as co-mesogens have been prepared and investigated as monomolecular layers at the water/air interface and as multilayer assemblies deposited onto solid supports by the Langmuir–Blodgett–Kuhn (LBK) technique. Pressure area isotherms at variable temperatures together with reflection absorption spectra and Brewster angle microscopic pictures have been taken and analyzed (i) to derive information about the structural order and the packing properties of the mesogenic side groups within the monolayers of different homo- and co-polymeric systems and ii) t…

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

Photoimaging through in-Situ Photopolymerization of Heterobifunctional Mesogenic Compounds in Liquid Crystalline State

2007

A series of heterobifunctional mesogenic biphenyl esters having two different polymerizable groups, i.e., acryl and diacetylene groups, were synthesized and their thermal behaviors and polymerization investigated. All compounds showed enantiotropic transitions. Under POM, highly birefringent focal-conic fan textures appeared on heating and cooling from the isotropic melt. Compounds 6−8 having a butyl spacer between a biphenyl and a diacetylene group exhibited LC phases even at room temperature. The X-ray diffractograms of compounds 6−8 showed a set of reflections in the small-angle region. They consisted of more than three sharp diffraction peaks with d spacings in the ratio of 1:1/2:1/3, s…

1978

1987

The dielectric relaxation properties of a combined main-chain/side-chain liquid-crystalline polymer were investigated. It was found that the rotation of the side chain about the main chain (δ-process) is not as strongly restricted as in side-chain liquid-crystalline polymers. This is attributed to the facts that the side chain is attached to the flexible spacer within the chain backbone and that the concentration of the side chains is comparatively small. Two low-temperature relaxation processes were observed to occur in the glassy smectic and the crystalline state. They are attributed to intramolecular motions with in the mesogenic groups.

Structure and Dilution of Mesogenic Side Chains in Liquid Crystalline Polysiloxanes

1988

Abstract The structure of the smectic phases in four series of homo- and copolymers based on dimethylsiloxane chains with a definite variation of the concentration of the paired mesogenic side chains has been investigated by means of X-ray methods. The dilution of the mesogenic moiety was achieved by insertion of additional dimethylsiloxane segments. A nearly linear dependence of the layer spacings on the dilution has been found. A model of the structure is proposed which consists of two sublayers one of which contains the irregularly arranged main chain whereas the other one is formed by the side chains.

1986

The molecular order and mobility of two liquid-crystalline polyacrylates with phenyl benzoate moieties as mesogenic side groups and (CH2)m spacers (m = 2 and m = 6) were investigated by pulsed 2H NMR. The mesogenic side groups were isotopically labelled at the terminal phenylene ring. In the glassy state the orientational distribution function was characterized from the angular dependence of the 2H NMR line shape of samples macroscopically ordered in their nematic phase by the 8,4 T magnetic field of an NMR spectrometer. It was found to be Gaussian with widths of ± 18,5° and ± 10,5° for the m = 2 frozen nematic and m = 6 frozen smectic system, respectively. The phenylene rings undergo 180° …

1985

Nonlinear optical self diffraction effects for a light beam in a liquid crystalline polymer in its isotropic fluid state was observed. This effect is characterized by the absence of a threshold intensity, a diffraction pattern that does not depend on the polarization of the reading beam relative to that of the writing beam and which cannot be disturbed by transversally applied static electrical fields. This effect is attributed to a thermally induced spatial refractive index modulation. The time constants of the response are of the order of ms.

Control of mesogen configuration in colloids of liquid crystalline polymers

2010

We report on a method to chemically predetermine the surface anchoring of mesogens in liquid crystalline colloids formed by different types of dispersion polymerization, and hence to achieve control over the mesogen configuration in such colloids. The surface anchoring is controlled by the chemical linkage of the polymers forming the colloids to the surfactants stabilizing the colloids towards the dispergent. We find that the hydroxypropyl cellulose used in conventional dispersion poylmerization induces parallel mesogen surface anchoring that in turn leads to bipolar director-field configurations, while a methacrylate terminated polysiloxane stabilizer, which is used in nonpolar dispersion …