Formation of P,C-chelated palladium complexes by phosphine-assisted oxidative addition of an aliphatic CCl bond

Portnoy Moshe, Yehoshua Ben-David, David Milstein

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Reactions of the (chloralkyl) phosphine 1-chloro-3-(diisopropylphosphino)propane (3) with chelated Pd(0) complexes have been given, leading to P,C-chelated complexes. Reaction of a methyl-π-allypalladium chloride dimer with 1,3-(diisopropylphosphino)propane and a base gives the binuclear complex 2a. Pd(dippe)2 (dippe = 1,2-bis(diisopropylphosphino)ethane) reacts with 3 to yield the mononuclear bis-chelated complex 6. As expected, the intramolecular coordinatively oxidative addition of the aliphatic CCl bond in 3 to the metal center is much faster than that of the intermolecular reaction of n-butyl chloride. The X-ray structure of 2a was determined.

Original languageEnglish
Pages (from-to)149-153
Number of pages5
JournalJournal of Organometallic Chemistry
Volume503
Issue number1
Publication statusPublished - Nov 1 1995

Fingerprint

phosphine
Propane
Palladium
phosphines
palladium
Methyl Chloride
propane
Ethane
Dimers
methyl chloride
Metals
X-Rays
X rays
ethane
chlorides
dimers
metals
x rays

Keywords

  • Alkyl chloride
  • Chelate
  • Metallation
  • Oxidative addition
  • Palladium

ASJC Scopus subject areas

  • Materials Chemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Biochemistry

Cite this

Formation of P,C-chelated palladium complexes by phosphine-assisted oxidative addition of an aliphatic CCl bond. / Moshe, Portnoy; Ben-David, Yehoshua; Milstein, David.

In: Journal of Organometallic Chemistry, Vol. 503, No. 1, 01.11.1995, p. 149-153.

Research output: Contribution to journalArticle

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