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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 is 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 allow us to exclude 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 electron to LUMO with the formation of a dissociative excited state according to quantum-chemical modeling, which provides novel opportunities for the fine control of reactivity using plasmon energy.
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http://dx.doi.org/10.1021/acs.jpclett.0c01350 | DOI Listing |
Chemistry
August 2025
MTA-ELTE "Lendület" Catalysis and Organic Synthesis Research Group, Eötvös Loránd University, Pázmány Péter stny. 1/A, Budapest, 1117, Hungary.
The development and mechanistic investigation of a novel O-fluoroalkylation of phenol derivatives using a hypervalent fluoroalkyliodonium salt, derived from hydrofluoroolefin gas (HFO-1234yf) as bulk fluorous feedstock, is reported. Optimization of the reaction conditions enabled versatile and efficient synthetic applications, and the synthetic study revealed phenol acidity-dependent selectivity of the O-fluoroalkylation process. The mechanistic behavior of phenols was supported by both experimental studies and DFT calculations.
View Article and Find Full Text PDFJ Org Chem
August 2025
Institute of Chemistry, Saint Petersburg State University, Universitetskaya Nab. 7/9, Saint Petersburg 199034, Russian Federation.
Hypervalent halonium salts are versatile arylating agents. While the reactivity of iodonium salts is well-studied, the reactivity of bromonium and chloronium salts remains underexplored. Here, we investigate the interplay between σ-hole coordination and aryl transfer in cyclic chloronium and bromonium salts, demonstrating how external anions modulate their reactivity and the regioselectivity of their transformations.
View Article and Find Full Text PDFOrg Lett
August 2025
Guangxi Key Laboratory of Electrochemical and Magneto-Chemical Functional Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004, China.
Copper/organic base-mediated dual -arylation of -amino carbazoles with cyclic diaryliodonium salts at room temperature has been unlocked, yielding nonsymmetric ,-bicarbazoles with a broad scope, especially tolerating all halogens (F, Cl, Br, and I). Besides, -amino indole, pyrrole, piperidine, morpholine, and piperazines all proved to be suitable coupling partners. The bottom-up access from inorganic hydrazine and cyclic iodoniums through double N-I exchange is also presented.
View Article and Find Full Text PDFJ Org Chem
August 2025
Department of Chemistry, Portland State University, Portland, Oregon 97201, United States.
Aryl(TMP)iodonium triflates are potentially useful reagents for metal-free arylation reactions. However, current syntheses require anion exchange reactions from the corresponding tosylate salts, which require additional time, materials and cost. Herein, we describe a direct, one-pot method to synthesize aryl(TMP)iodonium triflates by using triflic acid as one of the reagents; >20 examples are described in yields ranging between 55-90%.
View Article and Find Full Text PDFBeilstein J Org Chem
July 2025
Research School of Chemistry and Applied Biomedical Sciences, Tomsk Polytechnic University, Lenina Avenue 30, Tomsk, 634050, Russian Federation.
The arylation of isonitriles by diaryliodonium salts under photoredox conditions has been proposed for the first time. The suggested procedure allows preparing a broad range of benzamides using both symmetric and unsymmetric diaryliodonium salts under mild conditions. A plausible mechanism for the reaction and the selectivity of aryl transfer (in case of unsymmetrical iodonium salts) were studied.
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