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Updated: Jun 13, 2025

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Visible light-driven molecular oxygen activation for oxidative amidation of alcohols using lead-free metal halide
Vishesh Kumar1, Ved Vyas1, Deepak Kumar1
1Department of Chemistry, Indian Institute of Technology (BHU) Varanasi UP 221005 India arindam.chy@iitbhu.ac.in +919919080675.
Abstract:
Herein, we report the modulation of the band structures of halide perovskite Cs2CuBr4 by tuning the synthesis methods. The photocatalyst PC-1, synthesized by the hot injection method, has a more negative conduction band minima (CBM) than the photocatalyst PC-2, synthesized at room temperature. As a result, PC-1 can activate molecular O2 more efficiently to initiate the radical-mediated dehydrogenation of alcohols. The more positive valence band maxima (VBM) of PC-1 also facilitates amine oxidation to the corresponding radical. Further, improved charge separation and transport and a decrement in the photogenerated charge carrier recombination have been detected for PC-1 to enhance photocatalytic activity. PC-1 showed improved yields for a series of structurally diverse amides (highest yield = 98%) by oxidative amidation of alcohols under visible light irradiation.
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