Photochemistry of Surface-Confined Mononuclear and Trinuclear Ruthenium Carbonyl Complexes. Direct Evidence for the Ability to Isolate Photogenerated Intermediates from each other on High Surface Area Silica.

Abstract

Photoactivation of homogeneous organometallic catalysts by light-induced extrusion of 2-electron donor ligands or metal-metal bond cleavage has been demonstrated. A problem that has arisen is that the reactive solution species can recombine with the extruded ligand or can react with each other to form inactive clusters. We now report the synthesis and photochemical behavior of LRu(CO)4 and L3Ru3(CO)9 confined to the surface of high surface area silica. The results illustrates that immobilization of precursors to coordinatively unsaturated species prevents cluster formation, when the surface coverage is sufficiently low. Further, photodeclusterification of anchored L3Ru3(CO)9 is reversible due to the immobilization of the fragments.

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Document Details

Document Type
Technical Report
Publication Date
Jan 04, 1982
Accession Number
ADA110082

Entities

People

  • David K. Liu
  • Mark S. Wrighton

Organizations

  • Massachusetts Institute of Technology

Tags

Communities of Interest

  • Energy and Power Technologies
  • Weapons Technologies

DTIC Thesaurus Topics

  • Absorption
  • California
  • Carbonyl Complexes
  • Chemistry
  • Engineering
  • Illinois
  • Massachusetts
  • Materials
  • Materials Science
  • Metal Metal Bonds
  • Military Research
  • New York
  • North Carolina
  • Photochemistry
  • Spectra
  • United States
  • United States Government

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Theoretical Analysis.

Technology Areas

  • Microelectronics