| Literature DB >> 31233240 |
Philipp Weis1, Andreas Hess1,2, Gunnar Kircher1, Shilin Huang1,3, Günter K Auernhammer1,4, Kaloian Koynov1, Hans-Jürgen Butt1, Si Wu5,1.
Abstract
Photoisomerization in some azobenzene-containing polymers (azopolymers) results in reversible solid-to-liquid transitions because trans- and cis-azopolymers have different glass transition temperatures. This property enables photoinduced healing and processing of azopolymers with high spatiotemporal resolution. However, a general lack of knowledge about the influence of the polymer structure on photoinduced reversible solid-to-liquid transitions hinders the design of such novel polymers. Herein, the synthesis and photoresponsive behavior of new azopolymers with different lengths of spacers between the polymer backbone and the azobenzene group on the side chain are reported. Azopolymers with no and 20 methylene spacers did not show photoinduced solid-to-liquid transitions. Azopolymers with 6 or 12 methylene spacers showed photoinduced solid-to-liquid transitions. This study demonstrates that spacers are essential for azopolymers with photoinduced reversible solid-to-liquid transitions, and thus, gives an insight into how to design azopolymers for photoinduced healing and processing.Entities:
Keywords: azobenzenes; isomerization; photochemistry; polymers; self-healing
Year: 2019 PMID: 31233240 DOI: 10.1002/chem.201902273
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236