Pt<sup>II</sup>-Catalyzed Ethylene Hydrophenylation: Influence of Dipyridyl Chelate Ring Size on Catalyst Activity and Longevity

  • Bradley A. McKeown (1950541)
  • Hector Emanuel Gonzalez (1933489)
  • T. Brent Gunnoe (1438375)
  • Thomas R. Cundari (628766)
  • Michal Sabat (1385655)
Publication date
June 2013

Abstract

Expansion of the dipyridyl ligand from a five- to six-membered chelate for Pt<sup>II</sup>-catalyzed ethylene hydrophenylation provides an enhancement of catalyst activity and longevity. Mechanistic studies of [(dpm)­Pt­(Ph)­(THF)]­[BAr′<sub>4</sub>] [dpm = 2,2′-dipyridylmethane, and Ar′ = 3,5-(CF<sub>3</sub>)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>] attribute the improved catalytic performance at elevated temperatures to a favorable change in entropy of activation with an increase in chelate ring size. The Pt<sup>II</sup> catalyst precursor [(dpm)­Pt­(Ph)­(THF)]­[BAr′<sub>4</sub>] is among the most active catalysts for ethylene hydrophenylation by a non-acid-catalyzed mechanism

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