Investigation of Metal-dπ-Butadiynyl-π Interactions in (η5-C5H5)(CO)2FeCCCCH Using Photoelectron Spectroscopy

Dennis L. Lichtenberger, Sharon K. Renshaw, Andrew Wong, Christopher D. Tagge

Research output: Contribution to journalArticlepeer-review

93 Scopus citations

Abstract

The electronic structure of (η5-C5H5)(CO)2FeCCCCH (1) is investigated with gas-phase He I and He II photoelectron spectroscopy (PES). A central issue is the electronic communication from the metal through the poly-yne chain. The spectra show distinct ionization bands (ionizations) that originate from the metal d6 orbitals, the occupied butadiynyl π orbitals, the cyclopentadienyl e1″ orbitals, and the iron-butadiynyl σ bond. Metal-dπ-butadiynyl-π electronic interactions are indicated by the splitting pattern of the iron-based ionizations and from changes in ionization cross sections from He I to He II excitation, which indicate the predominant character of ionizations. The CCCCH (butadiynyl) ligand is best described as a net π donor ligand, and in this case the occupied butadiynyl π orbitals interact with occupied metal dπ orbitals in filled/filled type interactions. The mixing between occupied metal dπ and butadiynyl π orbitals is extensive, and the π system of 1 can be thought of as a five-centered poly-yne. Results from Fenske-Hall and extended Hückel calculations agree with the information obtained from PES and also give additional information about orbital coefficients and charges of the CCCCH π system. The spectrum of 1 is also compared to that of (η5-C5H5)(CO)2FeCCH, and the separate σ and π bonding components of the CCH and CCCCH ligands are evaluated.

Original languageEnglish (US)
Pages (from-to)3522-3526
Number of pages5
JournalOrganometallics
Volume12
Issue number9
DOIs
StatePublished - Jan 1 1993

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

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