Science · 1997 · 270 citations · 27 references
Natural SciencesChemistryChemical KineticsPhysical ChemistryTheoretical ChemistryChemical Reaction KineticsChemical ThermodynamicsMolecular BondingReaction DynamicsReaction MechanismsBarriersC-h ActivationC-h Bond ActivationCarbon-hydrogen ActivationHydride FormationMetal Alkyl Hydride IntermediatesMild Reaction ConditionsTime-resolved Infrared Spectroscopy
Chemical reactions that break alkane carbon-hydrogen (C–H) bonds are normally carried out under conditions of high temperature and pressure because these bonds are extremely strong (∼100 kilocalories per mole), but certain metal complexes can activate C–H bonds in alkane solution under the mild conditions of room temperature and pressure. Time-resolved infrared experiments probing the initial femtosecond dynamics through the nano- and microsecond kinetics to the final stable products have been used to generate a detailed picture of the C–H activation reaction. Structures of all of the intermediates involved in the reaction of Tp*Rh(CO) 2 (Tp* = HB–Pz 3 *, Pz* = 3,5-dimethylpyrazolyl) in alkane solution have been identified and assigned, and energy barriers for each reaction step from solvation to formation of the final alkyl hydride product have been estimated from transient lifetimes.
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Gerhard Habermehl · Toxicon · 1983 · 3.1K citations
Activation of Alkanes with Organotransition Metal Complexes
Robert G. Bergman · Science · 1984 · 311 citations