光电开关
光异构化
光稳态
光化学
光致变色
靛蓝
波长
化学
光谱学
热稳定性
材料科学
辐照
光电子学
光学
异构化
有机化学
物理
量子力学
催化作用
核物理学
作者
Daria V. Berdnikova,Bernhard M. Kriesche,Thomas Paululat,Thomas S. Hofer
标识
DOI:10.1002/chem.202202752
摘要
Wavelength-independent conversion of organic photoswitches in the photostationary state is a rare phenomenon that opens up a way for many practical applications. In this work, three fused bis(hemi-indigo) derivatives with different substitution patterns were synthesized and their photoswitching was investigated by optical spectroscopy, real-time NMR spectroscopy and TD-DFT calculations. We disclosed that the Z-E photoisomerization of the meta-bis(hemi-indigo) derivative was remarkably independent of the irradiation wavelength from UV up to yellow light. The wavelength-independent forward photoswitching together with the inhibited backward photoisomerization, high thermal stability of the photoinduced isomers as well as significant overlap between the photoswitch absorption and the solar spectrum allows to suggest bis(hemi-indigo) derivatives as promising candidates for molecular solar thermal energy storage (MOST) systems.
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