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Übergangsmetall-methylen-komplexe. XXXI. Primärkomplexierung von diazoalkanen an metall-metall-mehrfachbindungen; ein weiterer koordinationstyp

  • Johann Wolfgang Goethe University
  • Heidelberg University

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

An unexpected novel coordination mode of diazoalkanes has been verified via addition of 2-diazopropane to the metal-metal triple bond of bis[dicarbonyl(η5-pentamethylcyclopentadienyl)molybdenum] (MoMo). The dinuclear 1:1 addition product isolated in nearly quantitative yield is structurally characterized by a bent, 4-electron type η12-diazoalkane ligand, with the terminal nitrogen atom symmetrically bridging the metal-metal "single bond" (d(MoMo) 305.0(2) pm; d(MoN(1)) 212.0(12) and 212.6(10) pm, respectively) and the second nitrogen atom being bonded to one molybdenum atom only (d(MoN(2)) 213.4(13) pm).

Original languageGerman
Pages (from-to)381-393
Number of pages13
JournalJournal of Organometallic Chemistry
Volume240
Issue number4
DOIs
StatePublished - 28 Dec 1982
Externally publishedYes

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