Synthesis of μ-phosphide diiron complexes having a P-H bond: Hydrophosphination of phenylacetylene and methyl acrylate with the cationic μ-phosphide diiron complex

Junji Sugiura, Taeko Kakizawa, Hisako Hashimoto, Hiromi Tobita, Hiroshi Ogino

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

Thermal reaction of Cp2Fe2(CO)4 with PRH2 (R = Ph, Mes (mesityl)) in refluxing toluene afforded phosphide- and hydrido-bridged diiron complexes Cp2Fe2(CO) 2(μ-H)(μ-PHR) (1a, R = Ph; 1b, R = Mes). Treatment of 1a with HOTf under a CO atmosphere produced the phosphide- and carbonyl-bridged cationic complex [Cp2Fe2(CO)2(μ-CO)(μ-PHPh)](OTf) (2) via hydride abstraction as hydrogen and CO coordination. Complex 2 reacted with phenyl-acetylene and methyl acrylate at room temperature to give [Cp 2Fe2(CO)2(μ-CO)(μ-(E)-PPh-(CH=CHPh))] (OTf) (3a) and [Cp2Fe2(CO)2(μ-CO)(μ- P(CH2CH2CO2Me)Ph)](OTf) (3b) in 78% and 65% yield, respectively, in the absence of any additive, as a result of hydrophosphination of the unsaturated carbon-carbon bond of the substrates with the P-H bond of 2.

Original languageEnglish
Pages (from-to)1099-1104
Number of pages6
JournalOrganometallics
Volume24
Issue number6
DOIs
Publication statusPublished - 2005 Mar 14

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

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