Kinetic investigation of a PC(sp(3))P pincer palladium (II) complex in the Heck reaction

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Abstract

An investigation of the kinetics of the Heck reaction between 4-iodoanisole and styrene catalysed by {cis-1,3-bis[(di-tert-butylphosphino)methyl]-cyclohexane} palladium (11) iodide (1) has been performed in DMF-d(7) solution. Based on mercury poisoning experiments a heterogeneous palladium catalyst formed from the PCsp3P Pd(II) pre-catalyst is proposed. Saturation behaviour with respect to the olefin concentration suggests a mechanism consisting of a pre-equilibrium association of the olefin followed by a rate determining reaction with aryl halide. The equilibrium constant for the olefin association, K-1, and the rate constant for the subsequent oxidative addition step, k(2), were determined to (5.7 +/- 2.5) x 10(-3) and 18.4 +/- 2.7 M-1 s(-1), respectively. (c) 2005 Elsevier B.V. All rights reserved.

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  • Organic Chemistry
Original languageEnglish
Pages (from-to)4197-4202
JournalJournal of Organometallic Chemistry
Volume690
Issue number18
Publication statusPublished - 2005
Publication categoryResearch
Peer-reviewedYes

Bibliographic note

The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240), Department of Chemistry (011001220)