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腙类光开关的平面化诱导激活波长红移和热半衰期加速。

Planarization-Induced Activation Wavelength Red-Shift and Thermal Half-Life Acceleration in Hydrazone Photoswitches.

机构信息

Department of Chemistry Dartmouth College, 6128 Burke Laboratory Hanover New Hampshire 03755 USA.

出版信息

ChemistryOpen. 2020 Feb 3;9(2):191-194. doi: 10.1002/open.201900340. eCollection 2020 Feb.

Abstract

The optimization and modulation of the properties of photochromic compounds, such as their activation wavelengths and thermal relaxation half-lives (), are essential for their adaptation in various applications. In this work, we studied the effect of co-planarization of the rotary fragment of two photochromic hydrazones with the core of the molecule on their switching properties. The and isomers of both compounds exhibit red-shifted absorption bands relative to their twisted versions, allowing for their photoswitching using longer wavelengths of light. Additionally, the thermal half-lives of both hydrazones are drastically shortened from hundreds of years to days.

摘要

对光致变色化合物性质的优化和调节,例如其激活波长和热弛豫半衰期(),对于它们在各种应用中的适应至关重要。在这项工作中,我们研究了两个光致变色腙的旋转片段与分子核心共面化对其开关性质的影响。这两种化合物的和异构体相对于其扭曲形式具有红移的吸收带,这使得它们可以使用更长波长的光进行光致变色。此外,两种腙的热半衰期都从数百年急剧缩短到几天。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a376/6996581/77a1bfc7a750/OPEN-9-191-g003.jpg

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