Photochemistry of Cobalt Carbonyl Complexes having a Cobalt-Silicon Bond and its Importance in Activation of Catalysis.

Abstract

Photochemistry of R3SiCo(CO)4 (R = Et, Ph) in hydrocarbon solvents shows that the dominant primary excited state process is loss of CO, not cleavage of the Si-Co bond. The 366 nm quantum yield for CO substitution by P(OPh)3 is 0.28 + or - 0.05 to give R3SiCo(CO)3P(OPh)3. Regeneration of catalytic activity in the Co2(CO)8/1-pentene/HSiEt3 system can be accomplished photochemically by exciting the Et3SiCo(CO)4 species.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Aug 22, 1980
Accession Number
ADA088608

Entities

People

  • Carol L. Reichel
  • Mark S. Wrighton

Organizations

  • Massachusetts Institute of Technology

Tags

Communities of Interest

  • Advanced Electronics
  • Energy and Power Technologies
  • Weapons Technologies

DTIC Thesaurus Topics

  • Alkenes
  • Carbonyl Complexes
  • Chemical Compounds
  • Chemical Engineering
  • Chemical Synthesis
  • Chemistry
  • Hydrocarbons
  • Inorganic Chemistry
  • Massachusetts
  • Materials
  • Materials Science
  • Military Research
  • New Jersey
  • New York
  • Quantum Yields
  • Spectra
  • United States

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Surface Engineering/Surface Coating Technology.

Technology Areas

  • Quantum Computing