Journal
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Volume 337, Issue -, Pages 19-24Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2017.01.002
Keywords
Carbonylative Suzuki reaction; DMF decomposition; CO surrogates; Photocatalysis; Titanium dioxide
Categories
Funding
- NSFC [21273035]
- 973 Programs [2014CB239303]
- Award Program for Minjiang Scholar Professorship
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A light-induced carbonylative Suzuki reaction to produce diaryl ketone was achieved over Pd(phen)Cl-2/TiO2 under mild condition via a successful coupling of TiO2-based photocatalytic decomposition of DMF to generate CO and the Pd-based catalysis. An optimum conversion of Phi of 89%, with a yield of 45% to the desired carbonylative diaryl ketone was achieved over irradiated Pd(phen)Cl-2/TiO2 under CO2 atmosphere. Although the side self-coupling of Phi to form biphenyl cannot be completely suppressed in the light-induced carbonylative reaction, the use of photocatalytic decomposition of DMF to in-situ generate CO as a self-supplied CO source still shows prospect in the synthesis of diaryl ketone and represents a new and promising strategy for realizations of carbonylative reactions. (C) 2017 Elsevier B.V. All rights reserved.
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