Controlled Diels-Alder "Click" Strategy to Access Mechanically Aligned Main-Chain Liquid Crystal Networks

被引:5
|
作者
Campos, Jesus Guillen [1 ]
Stricker, Friedrich [1 ]
Clark, Kyle D. [1 ]
Park, Minwook [1 ]
Bailey, Sophia J. [1 ]
Kuenstler, Alexa S. [2 ]
Hayward, Ryan C. [2 ]
de Alaniz, Javier Read [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Univ Colorado Boulder, Dept Chem & Biol Engn, Boulder, CO 80305 USA
基金
新加坡国家研究基金会; 美国国家科学基金会;
关键词
Click Chemistry; Cyclopentadiene; Diels-Alder; Liquid Crystal Networks; Two-Step Polymerization; SHAPE-MEMORY; ELASTOMERS; LIGHT;
D O I
10.1002/anie.202214339
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aligned liquid crystal polymers are materials of interest for electronic, optic, biological and soft robotic applications. The manufacturing and processing of these materials have been widely explored with mechanical alignment establishing itself as a preferred method due to its ease of use and widespread applicability. However, the fundamental chemistry behind the required two-step polymerization for mechanical alignment has limitations in both fabrication and substrate compatibility. In this work we introduce a new protection-deprotection approach utilizing a two-stage Diels-Alder cyclopentadiene-maleimide step-growth polymerization to enable mild yet efficient, fast, controlled, reproducible and user-friendly polymerizations, broadening the scope of liquid crystal systems. Thorough characterization of the films by DSC, DMA, POM and WAXD show the successful synthesis of a uniaxially aligned liquid crystal network with thermomechanical actuation abilities.
引用
收藏
页数:5
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