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追踪嵌入在结晶纳米多孔 MOF 孔中的螺吡喃的光诱导异构化过程和光稳定性 红外光谱法。

Tracking the light-induced isomerization processes and the photostability of spiropyrans embedded in the pores of crystalline nanoporous MOFs IR spectroscopy.

机构信息

Institute of General, Inorganic and Theoretical Chemistry, University of Innsbruck, Innrain 80-82, A-6020 Innsbruck, Austria.

Université de Lorraine, CNRS, CRM2, F-54000 Nancy, France.

出版信息

Photochem Photobiol Sci. 2020 Oct 14;19(10):1433-1441. doi: 10.1039/d0pp00267d.

Abstract

The embedment of photochromic dyes into porous host matrices has attracted increasing interest in recent years. Especially the class of spiropyrans has been considered because of its outstanding photochromic and solvatochromic response. We herein present a comprehensive infrared spectroscopic characterization of the photoresponse and photostability of a nitro-substituted spiropyran "SP-Nitro" (namely 1,3,3-trimethylindolino-6'-nitrobenzopyrylospiran) non-covalently attached to different crystalline nanoporous MOF (metal-organic framework) host lattices. The TTC mesomeric form of SP-Nitro has been found to be preferably generated upon UV light exposure inside the different MOF hosts. Additionally, the excited isomer was found to be stable for prolonged irradiation times of 1-1.5 h.

摘要

近年来,将光致变色染料嵌入多孔主基质中引起了越来越多的关注。特别是螺吡喃类因其出色的光致变色和溶剂化响应而受到关注。本文综合了对硝基取代螺吡喃“SP-Nitro”(即 1,3,3-三甲基吲哚啉-6'-硝基苯并吡喃螺吡喃)的光响应和光稳定性的红外光谱表征,该螺吡喃非共价键合到不同的结晶纳米多孔 MOF(金属-有机骨架)主晶格上。已经发现,在不同的 MOF 主体中,SP-Nitro 的 TTC 中间态形式在紫外光照射下更容易生成。此外,还发现激发态异构体在 1-1.5 小时的长时间辐照下稳定。

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