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Plasmon-assisted transformations of organic compounds represent a novel opportunity for conversion of light to chemical energy at room temperature. However, the mechanistic insights of interaction between plasmon energy and organic molecules are still under debate. Herein, we proposed a comprehensive study of the plasmon-assisted reaction mechanism using unsymmetric iodonium salts (ISs) as an organic probe. The experimental and theoretical analysis allows excluding the possible thermal effect or hot electron transfer. We found that plasmon interaction with unsymmetrical ISs led to the intramolecular excitation of electron followed by the regioselective cleavage of C-I bond with the formation of electron-rich radical species, which cannot be explained by the hot electron excitation or thermal effects. The high regioselectivity is explained by the direct excitation of the electron to LUMO with the formation of the dissociative excited state according to quantum-chemical modeling, which provides a novel opportunities to the fine control of reactivity using plasmon energy.
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10.1021/acs.jpclett.0c01350
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The_journal_of_physical_chemistry_letters
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Сan Plasmon Change Reaction Path? Decomposition of Unsymmetrical Iodonium Salts as an Organic Probe.
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