Villabona Marc, Wiedbrauk Sandra, Feist Florian, Guirado Gonzalo, Hernando Jordi, Barner-Kowollik Christopher
Department de Química, Universitat Autònoma de Barcelona, Edifici C/n, Campus UAB, 08193 Cerdanyola del Vallès, Spain.
Centre for Materials Science, School of Chemistry and Physics, Queensland University of Australia (QUT), 2 George Street, Brisbane, Queensland 4000, Australia.
Org Lett. 2021 Apr 2;23(7):2405-2410. doi: 10.1021/acs.orglett.1c00015. Epub 2021 Feb 23.
The control of chemical functionalization with orthogonal light stimuli paves the way toward manipulating materials with unprecedented spatiotemporal resolution. To reach this goal, we herein introduce a photochemical reaction system that enables two-color control of covalent ligation via an -Diels-Alder cycloaddition between two separate light-responsive molecular entities: a UV-activated photocaged diene based on -quinodimethanes and a carbonyl dienophile appended to a diarylethene photoswitch, whose reactivity can be modulated upon illumination with UV and visible light.
利用正交光刺激控制化学官能化,为以前所未有的时空分辨率操纵材料铺平了道路。为了实现这一目标,我们在此引入一种光化学反应体系,该体系能够通过两个独立的光响应分子实体之间的狄尔斯-阿尔德环加成反应实现共价连接的双色控制:一种基于对醌二甲烷的紫外线激活的光笼二烯,以及连接到二芳基乙烯光开关上的羰基亲双烯体,其反应活性可在紫外线和可见光照射下进行调节。