6533b860fe1ef96bd12c38c9
RESEARCH PRODUCT
An unprecedented, bridged dihydrogen complex of a cofacial metallodiporphyrin and its relevance to the bimolecular reductive elimination of hydrogen
James P. CollmanPaul S. WagenknechtJames E. HutchisonMichel Angel LopezRoger GuilardNathan S. Lewissubject
Steric effectsLigandDimerchemistry.chemical_elementGeneral ChemistryReaction intermediateBiochemistryPorphyrinMedicinal chemistryCatalysisReductive eliminationRutheniumchemistry.chemical_compoundColloid and Surface ChemistrychemistryDihydrogen complexdescription
Recently, the authors characterized the first metalloporphyrin dihydrogen complex, Os(OEP)(H{sub 2}), and proposed that a similar ruthenium porphyrin dihydrogen complex, Ru(OEP)(H{sub 2}), is involved as an intermediate in the catalytic H/D isotopic exchange between water and hydrogen. They now report that treatment of a metal-metal-bonded cofacial ruthenium porphyrin dimer with a sterically bulky ligand in the presence of hydrogen gas has yielded the first known complex containing a dihydrogen ligand bound between two metals. Such a bridged dihydrogen complex is proposed as an intermediate in the bimolecular elimination of dihydrogen from two metalloporphyrin hydrides.
year | journal | country | edition | language |
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1990-10-01 | Journal of the American Chemical Society |