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Zweikernige η5-pentamethylcyclopentadienyl-rhenium-komplexe mit einer chalkogenbrücke. Die molekülstruktur von [(η5-C5Me5)Re(CO)2]2(μ-Se)

  • Max Herberhold
  • , Bertram Schmidkonz
  • , Ulf Thewalt
  • , Abbas Razavi
  • , Helmut Schöllhorn
  • , Wolfgang A. Herrmann
  • , Christian Hecht
  • Universität Bayreuth
  • University of Ulm
  • Technical University of Munich

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

We report the synthesis and characterisation of binuclear η5-pentamethylcyclopentadienylrhenium complexes, [(η5-C5Me5)Re(CO)2]2(μ-E) (E = S (2), Se (3), Te (4)), containing a chalcogen bridge in addition to a ReRe bond. According to the X-ray structural analysis, 3 possesses approximately C2 molecular symmetry; the C5Me5 ring ligands occupy trans positions with respect to the central Re2Se unit [d(ReRe) 3.032(1) Å, {right parenthesis, less than} ReSeRe 74.9(1)°]. As expected, the complexes of the now complete series [Cp{black star}Re(CO)2]2(μ-E) (E = O (1), S (2), Se (3), Te (4)) show a high degree of similarity in their corresponding mass, IR, 1H and 13C NMR spectra.

Original languageGerman
Pages (from-to)213-221
Number of pages9
JournalJournal of Organometallic Chemistry
Volume299
Issue number2
DOIs
StatePublished - 21 Jan 1986

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