螺吡喃
汞菁
极性(国际关系)
光致变色
光异构化
胶粘剂
侧链
聚合物
材料科学
粘附
烷基
高分子化学
纳米技术
化学
有机化学
复合材料
异构化
图层(电子)
生物化学
细胞
催化作用
作者
Keiichi Imato,Koki Momota,Naoki Kaneda,Ichiro Imae,Yousuke Ooyama
标识
DOI:10.1021/acs.chemmater.2c01809
摘要
Photoswitchable polymer adhesives enable strong bonding and on-demand debonding with minimal damage to adherends due to the high spatiotemporal resolution and therefore promise to contribute to material recycling as complex architectures consisting of dissimilar materials are being developed in various fields. In a variety of photosystems, the photoisomerization between noncharged spiropyran (SP) and zwitterionic merocyanine (MC) with large polarity changes is a primary candidate because molecular polarity is a dominant factor to generate adhesion force. However, SP has not been chemically incorporated into polymer adhesives. In this study, we developed photoswitchable adhesives of SP homopolymers with different molecular mobility of the SPs, which were located in the side chains and linked to the main chains through alkyl spacers with different lengths. Photoswitching of the adhesion strength by the polarity changes between SP and MC was demonstrated on both hydrophilic and hydrophobic substrates.
科研通智能强力驱动
Strongly Powered by AbleSci AI