Mechanism for thermal generation of transient rhenium(0) radicals. Reaction of a (triphenylmethyl)rhenium complex with two-electron ligands

Lisa S. Crocker, Bruce M. Mattson, Bruce M. Mattson

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Reaction of (η3-CPh3)Re(CO)4 (1) with 2 equiv of the cage phosphite 1-methyl-4-phospha-3,5,8-trioxabicyclo[2.2.2]octane (MPTB) results in formation of mer-trans-Re(CO)3(MPTB) 2(4-(diphenylmethylene)cyclohexa-2,5-diene) (2a). In solution at 233 K, 2a isomerizes to the facial-cis isomer 2b. At higher temperatures, 2a and 2b decompose via metal-alkyl bond homolysis to give Ph3C radicals and the transient Re(0) radicals Re(C0)3(MPTB)2, which decompose. The reactivity of (η3-CPh3)Re(CO)4 toward other neutral two-electron phosphorus donor ligands is similar, but the corresponding rhenium-alkyl products Re(CO)3P2(4-(diphenylmethylene)cyclohexa-2,5-diene) could not be isolated from solution. Instead, they were derivatized with use of Ph3SnH or CCl4 to the corresponding hydrides or chlorides. Several mechanisms that could account for the observed reactivity of 1 with phosphines and phosphites to generate transient Re(0) radicals are discussed.

Original languageEnglish
Pages (from-to)1011-1016
Number of pages6
JournalOrganometallics
Volume9
Issue number4
StatePublished - 1990

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Rhenium
rhenium
Carbon Monoxide
dienes
Phosphites
Ligands
ligands
Electrons
reactivity
electrons
octanes
Phosphines
phosphines
hydrides
phosphorus
isomers
chlorides
Hydrides
Isomers
Phosphorus

All Science Journal Classification (ASJC) codes

  • Inorganic Chemistry
  • Organic Chemistry

Cite this

Mechanism for thermal generation of transient rhenium(0) radicals. Reaction of a (triphenylmethyl)rhenium complex with two-electron ligands. / Crocker, Lisa S.; Mattson, Bruce M.; Mattson, Bruce M.

In: Organometallics, Vol. 9, No. 4, 1990, p. 1011-1016.

Research output: Contribution to journalArticle

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AB - Reaction of (η3-CPh3)Re(CO)4 (1) with 2 equiv of the cage phosphite 1-methyl-4-phospha-3,5,8-trioxabicyclo[2.2.2]octane (MPTB) results in formation of mer-trans-Re(CO)3(MPTB) 2(4-(diphenylmethylene)cyclohexa-2,5-diene) (2a). In solution at 233 K, 2a isomerizes to the facial-cis isomer 2b. At higher temperatures, 2a and 2b decompose via metal-alkyl bond homolysis to give Ph3C radicals and the transient Re(0) radicals Re(C0)3(MPTB)2, which decompose. The reactivity of (η3-CPh3)Re(CO)4 toward other neutral two-electron phosphorus donor ligands is similar, but the corresponding rhenium-alkyl products Re(CO)3P2(4-(diphenylmethylene)cyclohexa-2,5-diene) could not be isolated from solution. Instead, they were derivatized with use of Ph3SnH or CCl4 to the corresponding hydrides or chlorides. Several mechanisms that could account for the observed reactivity of 1 with phosphines and phosphites to generate transient Re(0) radicals are discussed.

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