New smart materials: molecular simulation of nonlinear optical chromophore-containing polypeptides and liquid crystalline siloxanes

Author(s):  
Ruth Pachter ◽  
Soumya S. Patnaik ◽  
Robert L. Crane ◽  
W. Wade Adams
2021 ◽  
Vol 22 (11) ◽  
pp. 5740
Author(s):  
Ramón Cervera-Procas ◽  
José-Luis Serrano ◽  
Ana Omenat

Highly functional macromolecules with a well-defined architecture are the key to designing efficient and smart materials, and these polymeric systems can be tailored for specific applications in a diverse range of fields. Herein, the formation of a new liquid crystalline polymeric network based on the crosslinking of dendrimeric entities by the CuI-catalyzed variant of the Huisgen 1,3-dipolar cycloaddition of azides and alkynes to afford 1,2,3-triazoles is reported. The polymeric material obtained in this way is easy to process and exhibits a variety of properties, which include mesomorphism, viscoelastic behavior, and thermal contraction. The porous microstructure of the polymer network determines its capability to absorb solvent molecules and to encapsulate small molecules, like organic dyes, which can be released easily afterwards. Moreover, all these properties may be easily tuned by modifying the chemical structure of the constituent dendrimers, which makes this system a very interesting one for a number of applications.


2009 ◽  
Author(s):  
Azusa Inoue ◽  
Shin-ichiro Inoue ◽  
Shiyoshi Yokoyama ◽  
Keisuke Kojima ◽  
Kei Yasui ◽  
...  

2007 ◽  
Vol 3 (1) ◽  
pp. 50-53
Author(s):  
Li-kun Han ◽  
Ya-dong Jiang ◽  
Wei Li ◽  
Yuan Cai

1991 ◽  
Vol 6 (3) ◽  
pp. 604-609 ◽  
Author(s):  
R.B. Findlay ◽  
T.J. Lemmon ◽  
A.H. Windle

Characterizations of side chain liquid crystalline polymers and their monomers point toward chemical structures and processing techniques which optimize their suitability for nonlinear optical applications. Polymers with methacrylate backbones and nitrostilbene or nitrobiphenyl side groups are studied; they tend to form smectic phases, but no solid crystallinity. By copolymerizing with nonmesogenic backbone units, the smectic-isotropic transition temperature can be controlled and may fall below the glass transition temperature. There is evidence for a significant degree of pretransitional alignment due to the surface fields, and mesogen ordering perpendicular to flow-induced backbone alignment. Very rapid cooling can suppress the highly scattering polydomain smectic phase.


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