Kinetics and Mechanism of the Platinum(II)-Catalyzed Hydroarylation of Vinyl Arenes with 1,2-Dimethylindole

Journal Article (Journal Article)

The mechanism of the intermolecular hydroarylation of vinyl arenes (1) with 1,2-dimethylindole (2) catalyzed by PtCl has been evaluated through a combination of kinetic analysis, deuterium labeling studies, and stereochemical analysis. The results of these and additional experiments are consistent with a mechanism for hydroarylation involving rapid and reversible complexation of vinyl arene to the catalytically inactive platinum mono(vinyl arene)complex trans-PtCl (H C=CHAr)(solvent) to form the reactive platinum bis(vinyl arene) complex trans-PtCl (H C=CHAr) , which undergoes turnover-limiting, outer-sphere attack of indole. Rapid protodemetallation of the resulting platinum alkyl complex releases product and regenerates the equilibrating mixture of platinum π-vinyl arene complexes. 2 2 2 2 2 2

Full Text

Duke Authors

Cited Authors

  • Zhang, Z; Liu, S; Widenhoefer, RA

Published Date

  • March 1, 2020

Published In

Volume / Issue

  • 60 / 3-4

Start / End Page

  • 437 - 445

Electronic International Standard Serial Number (EISSN)

  • 1869-5868

International Standard Serial Number (ISSN)

  • 0021-2148

Digital Object Identifier (DOI)

  • 10.1002/ijch.201900065

Citation Source

  • Scopus