4.7 Article

Exploring Eosin Y as a bimodular catalyst: organophotoacid mediated Minisci-type acylation of N-heteroarenes

期刊

CHEMICAL COMMUNICATIONS
卷 58, 期 11, 页码 1776-1779

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cc06483e

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  1. SERB, India [SRG/2019/000404]
  2. CSIR [02(0416)/21/EMR-II]
  3. MHRD (GoI)

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In this study, Eosin Y was reported as a bimodular catalyst for Minisci-type acylation reactions. The formation of organic exciplexes between photoexcited Eosin Y and N-heteroarenes was found to stabilize photoacid catalysis under optimized conditions.
Here we report Eosin Y as a bimodular catalyst for Minisci-type acylation reactions. The formation of organic exciplexes between photoexcited Eosin Y and N-heteroarenes was found to be a stabilizing factor for photoacid catalysis under optimized conditions. Spectroscopic investigations such as steady state fluorescence quenching and dynamic lifetime quenching experiments were employed to better understand the role of Eosin Y as both a photoredox catalyst and a photoacid. Feedstock aldehydes were employed as acyl radical precursors for engaging in C-C bond formation reactions with a variety of nitrogen containing heterocycles.

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