Cyclic Liquid Crystalline Siloxanes - Chemistry and Applications

1996 ◽  
Vol 425 ◽  
Author(s):  
F.-H. Kreuzer ◽  
R. Maurer ◽  
J. Stohrer

AbstractCyclic Siloxanes, bearing mesogenic groups, connected with the backbone via aliphatic spacers exhibit phases analogue to the classic calamitics. Bearing two different mesogenic groups, these materials can be considered as cooligomers, whose degree of polymerization is given by the H-siloxanes used. These cooligomers consist of a mixture of molecules with substitution patterns determined by the statistics of the addition reaction of the mesogenic groups to the H-siloxane. Two types of materials are available, crosslinkable and non crosslinkable. As most important applications may be mentioned: Cholesteric reflectors and filters, storage materials for optical informations, retardation plates and pigments for iridescent or polarizing coatings.

2011 ◽  
Vol 217-218 ◽  
pp. 359-362
Author(s):  
Han Jian ◽  
Yie Guo

The molecule weight and distribution of molecule weight of a kind of medium temperature phenol formaldehyde resin(MTPF)was detected through Liquid Chromatogram-mass spectrum instrument(LC-MS).The result showed that the distribution scope of molecule weight of the MTPF during the initial stage was approximately 200-400,and the degree of polymerization of the MTPF molecule was 2-4,At the same time,the MTPF during initial stage still has a certain amount of medium outcome hydroxymethyl phenol which was formed through the addition reaction between phenol and formaldehyde.The detection result,from the MTPF during initial stage through ZEN3600 nanometer grain analysis instrument, proved that the grain size of the MTPF during initial stage was about 80-180nm,and the distribution of the grain size presented a normal one that the grain size 96-130nm was about 67%.


1995 ◽  
Vol 18 (1) ◽  
pp. 73-79 ◽  
Author(s):  
E. Novotná ◽  
S. G. Kostromin ◽  
H. Kresse

2020 ◽  
Vol 992 ◽  
pp. 386-391
Author(s):  
T.R. Deberdeev ◽  
L.K. Karimova ◽  
A.I. Akhmetshina

Liquid crystalline (LC) copolyesters derived from 4-hydroxybenzoic acid, terephthalic acid, and bisphenol A were synthesized under a variety of reaction conditions. Carboxylic groups in the raw materials were involved in either direct polycondensation or transesterification reactions. Protecting the carboxylic groups via methyl ester or phenyl ester formation was found to increase the yield and the molecular weight of the samples. It turned out that the maximal value of the degree of polymerization and, consequently, the highest heat resistance was observed for the samples prepared using phenyl esters of carboxylic acids.


2006 ◽  
Vol 460 (1) ◽  
pp. 23-33 ◽  
Author(s):  
Joanna T. Sołtysiak ◽  
Ewa Białecka-Florjańczyk

Liquid crystalline side-chain polymers are polymers that have linked conventional low molecular mass liquid crystals (I.e.) as side chains to a polymer backbone. Their properties are experimentally compared with the corresponding low molecular mass I.e. (i) Beginning with a monomeric I.e., with increasing degree of polymerization an increase of the phase transformation temperature of I.e. to isotropic is observed. (ii) The nematic order parameter of the monomers is about 10 % higher than the order parameter of the polymers. Owing to the linkage of the rigid mesogenic molecules to the polymer backbone, their rotation around the long molecular axis differs strongly from that of the monomers, (hi) Owing to the high viscosity of the polymers their response times in the electric field are much larger than the response times of the monomers. If a sufficient length of the flexible spacer that connects the mesogenic molecule to the polymer main chain is assumed, the threshold voltages of the monomers and polymers are of comparable magnitude.


1994 ◽  
Vol 27 (25) ◽  
pp. 7248-7253 ◽  
Author(s):  
L. V. Natarajan ◽  
T. J. Bunning ◽  
S. Y. Kim

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