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- W3017929971 abstract "Organic materials that show substantial reactivity under visible light have received considerable attention due to their wide applications in chemical and biological systems. Hemicyanine pigments possess a strong intramolecular donor–acceptor structure and thereby display intense absorption in the visible spectral region. However, most excitons are consumed via the twisted intramolecular charge-transfer (TICT) process, making hemicyanines generally inert to light. Herein, we describe the development of an amphiphilic hemicyanine dye whose aggregation could be easily regulated using salt or counterions. More importantly, its intrinsic photoreactivity was successfully induced by steric restriction and cofacial arrangement within the H-aggregate, thus creating an effective photobactericide. This strategy could be extended to the development of photocatalysts for photosynthesis and a photosensitizer for photodynamic therapy." @default.
- W3017929971 created "2020-05-01" @default.
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- W3017929971 date "2020-04-29" @default.
- W3017929971 modified "2023-10-16" @default.
- W3017929971 title "Aggregation-Dependent Photoreactive Hemicyanine Assembly as a Photobactericide" @default.
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- W3017929971 doi "https://doi.org/10.1021/acsami.0c03894" @default.
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