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具有高密集取代偶氮苯介晶元的间同立构侧链液晶聚合物的相行为和光响应薄膜

Phase Behaviors and Photoresponsive Thin Films of Syndiotactic Side-Chain Liquid Crystalline Polymers with High Densely Substituted Azobenzene Mesogens.

作者信息

Li Xiao, Zhao Weiguang, Jin Ye, Huang Jianjia, Chen Dongzhong

机构信息

Key Laboratory of High Performance Polymer Materials and Technology (Ministry of Education), Department of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Nanjing University, 210023, Nanjing, China.

School of Information Technology, Suzhou Institute of Trade & Commerce, 215009, Suzhou, China.

出版信息

Chemphyschem. 2024 Sep 16;25(18):e202400421. doi: 10.1002/cphc.202400421. Epub 2024 Jul 24.

DOI:10.1002/cphc.202400421
PMID:38825850
Abstract

Azobenzene-containing polymers (azopolymers) are a kind of fascinating stimuli-responsive materials with broad and versatile applications. In this work, a series of syndiotactic C1 type azopolymers of Pm-Azo-Cn with side-chain azobenzene mesogens of varied length alkoxy tails (n=1, 4, 8, 10) and different length alkyl spacers (m=6, 10) have been prepared via Rh-catalyzed carbene polymerization. The thermal properties and ordered assembly structures of thus synthesized side chain liquid crystalline polymers (SCLCPs) have been systematically investigated with differential scanning calorimetry (DSC), polarized optical microscopy (POM) and variable-temperature small/wide-angle X-ray scattering (SAXS/WAXS) analyses. P10-Azo-C1 and P10-Azo-C4 with shorter alkoxy tails exhibited hierarchical structures SmB/Col and transformed into SmA/Col at a higher temperature, while P10-Azo-C8 and P10-Azo-C10 with longer alkoxy tails only displayed side group dominated layered SmB phase and transformed into SmA phase at higher temperatures. For P6-Azo-C4 with a shorter spacer only showed a less ordered SmA phase owing to interference by partly coupling between the side chain azobenzene mesogens and the helical backbone. More importantly, the series high densely substituted syndiotactic C1 azopolymer thin films, exhibited evidently and smoothly reversible photoresponsive properties, which demonstrated promising photoresponsive device applications.

摘要

含偶氮苯的聚合物(偶氮聚合物)是一类极具吸引力的刺激响应材料,具有广泛多样的应用。在本工作中,通过铑催化的卡宾聚合反应制备了一系列间同立构C1型偶氮聚合物Pm-Azo-Cn,其侧链偶氮苯液晶基元具有不同长度的烷氧基尾链(n = 1、4、8、10)和不同长度的烷基间隔基(m = 6、10)。利用差示扫描量热法(DSC)、偏光显微镜(POM)和变温小角/广角X射线散射(SAXS/WAXS)分析系统地研究了如此合成的侧链液晶聚合物(SCLCPs)的热性能和有序组装结构。具有较短烷氧基尾链的P10-Azo-C1和P10-Azo-C4呈现出层状结构SmB/Col,并在较高温度下转变为SmA/Col,而具有较长烷氧基尾链的P10-Azo-C8和P10-Azo-C10仅显示侧基主导的层状SmB相,并在较高温度下转变为SmA相。对于具有较短间隔基的P6-Azo-C4,由于侧链偶氮苯液晶基元和螺旋主链之间的部分耦合干扰,仅显示出有序性较低的SmA相。更重要的是,该系列高密集取代的间同立构C1偶氮聚合物薄膜表现出明显且平滑的可逆光响应性能,这表明其在光响应器件应用方面具有广阔前景。

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