Kekulé-Institut für Organische Chemie und Biochemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhard-Domagk-Str. 1, 53121 Bonn, Germany.
Institut für Anorganische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhard-Domagk-Str. 1, 53121 Bonn, Germany.
Org Biomol Chem. 2023 Jun 21;21(24):4993-4998. doi: 10.1039/d3ob00413a.
Incorporation of azobenzenes into macrocycles is an intriguing approach for fine tuning the photophysical properties of these photoswitches and tailoring them to specific applications. A versatile synthesis of macrocyclic azobenzenes has been developed that allows for facile modification of these photoswitches. One example shows high chemical stability, long half-life of its -isomers, quantitative → conversion under white light, and excellent separation of excitation bands to address either the or -state selectively. The near quantitative → conversion under white light is a unique feature with an important impact on applications, in which the configuration under ambient light needs to be close to 100%.
将偶氮苯基团引入大环中是一种巧妙的方法,可以精细调节这些光开关的光物理性质,并将其调整到特定的应用中。已经开发出一种通用的大环偶氮苯合成方法,可方便地对这些光开关进行修饰。其中一个例子显示出了高化学稳定性、长的顺式异构体半衰期、在白光下定量的 → 转化,以及激发带的优异分离,以选择性地寻址 或 -态。在白光下近定量的 → 转化是一个独特的特性,对应用有重要影响,因为在环境光下的构型需要接近 100%。