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This research demonstrates enhanced photoswitching properties in N-alkyl imines, suggesting innovative design of photoresponsive structures.
High Resolution Image Download MS PowerPoint Slide N -Alkyl imines are prevalent in dynamic-covalent chemistry and self-assembled structures, yet their E / Z photochromism is often overlooked due to the high-energy light required for isomerization. Here, we present a simple strategy to enhance their photoswitching properties, achieving switching wavelengths and photostationary state distributions comparable to azobenzene. Moreover, we demonstrate that these N -alkyl imines undergo photoisomerization in the condensed phase and exhibit isomer-dependent fluorescence. We anticipate that this study will inspire the design of photoresponsive architectures that operate directly at the dynamic-covalent bond, eliminating the need for dedicated photoswitchable motifs.
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Wu et al. (2025) studied this question.
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