Li Peiqi, Tan Shuai, Wu Yong, Wang Caihong, Watanabe Masayoshi
Department of Chemical Machinery and Control Engineering, School of Chemical Engineering, Sichuan University, Sichuan 610065, China.
Department of Chemistry and Biotechnology, Yokohama National University, Yokohama 240-8501, Japan.
ACS Macro Lett. 2020 Jun 16;9(6):825-829. doi: 10.1021/acsmacrolett.0c00170. Epub 2020 May 20.
This paper presents a light-switchable phase separation of poly(-isopropylacrylamide) (PNIPAm) in aqueous solutions using an azobenzene-based ionic liquid as a molecular trigger. A different UV response was obtained with use of an azobenzene molecular trigger. A UV-induced aggregation of PNIPAm was observed in the current system, which is opposite to that reported for azobenzene-functionalized PNIPAm systems. According to FT-IR, -isomers destabilized the hydrogen bonding between water and PNIPAm, contributing to a light-induced aggregation of PNIPAm. This polarity effect was quite similar to salting effects of hofmeister anions on clouding points. Furthermore, a UV shutdown of ion transport of the azobenzene-based ionic liquid was demonstrated with a significant reduction factor of 0.03 at ambient temperature, which can be potentially applied in biotechnology, optoelectronics, and ionic circuits.
本文介绍了一种使用基于偶氮苯的离子液体作为分子触发器,在水溶液中实现聚(N-异丙基丙烯酰胺)(PNIPAm)的光开关相分离。使用偶氮苯分子触发器获得了不同的紫外响应。在当前体系中观察到PNIPAm的紫外诱导聚集,这与报道的偶氮苯功能化PNIPAm体系相反。根据傅里叶变换红外光谱,反式异构体破坏了水与PNIPAm之间的氢键,导致PNIPAm发生光诱导聚集。这种极性效应与霍夫迈斯特阴离子对浊点的盐析效应非常相似。此外,在室温下证明了基于偶氮苯的离子液体的离子传输的紫外关闭,其显著降低因子为0.03,这在生物技术、光电子学和离子电路中具有潜在应用。