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多孔有机框架中的正交光开关效应

Orthogonal Photoswitching in a Porous Organic Framework.

作者信息

Sheng Jinyu, Perego Jacopo, Bracco Silvia, Cieciórski Piotr, Danowski Wojciech, Comotti Angiolina, Feringa Ben L

机构信息

Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, Netherlands.

Present address: Institute of Science and Technology Austria, Am Campus 1, 3400, Klosterneuburg, Austria.

出版信息

Angew Chem Int Ed Engl. 2024 Jun 3;63(23):e202404878. doi: 10.1002/anie.202404878. Epub 2024 Apr 25.

Abstract

The development of photoresponsive systems with non-invasive orthogonal control by distinct wavelengths of light is still in its infancy. In particular, the design of photochemically triggered-orthogonal systems integrated into solid materials that enable multiple dynamic control over their properties remains a longstanding challenge. Here, we report the orthogonal and reversible control of two types of photoswitches in an integrated solid porous framework, that is, visible-light responsive o-fluoroazobenzene and nitro-spiropyran motifs. The properties of the constructed material can be selectively controlled by different wavelengths of light thus generating four distinct states providing a basis for dynamic multifunctional materials. Solid-state NMR spectroscopy demonstrated the selective transformation of the azobenzene switch in the bulk, which in turn modulates N and CO adsorption.

摘要

利用不同波长的光进行非侵入性正交控制的光响应系统的发展仍处于起步阶段。特别是,集成到固体材料中的光化学触发正交系统的设计,能够对其性质进行多重动态控制,这仍然是一个长期存在的挑战。在这里,我们报告了在一个集成的固体多孔框架中对两种类型的光开关进行正交和可逆控制,即可见光响应的邻氟偶氮苯和硝基螺吡喃基序。所构建材料的性质可以通过不同波长的光进行选择性控制,从而产生四种不同的状态,为动态多功能材料提供了基础。固态核磁共振光谱表明,本体中的偶氮苯开关发生了选择性转变,进而调节了氮和一氧化碳的吸附。

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