FT-EPR Study of Alkyl radicals formed in the photochemical reaction of Re(alkyl)(-diimine) and Ru(alkyl)(-diimine) complexes

C.J. KLEVERLAAN; D.M. MARTINO; JORIS VAN SLAGEREN; H. VAN WILLIGEN; D.J. STUFKENS; A. OSKAM

Applied magnetic Resonance

Año: 1998 vol. 15 p. 203 - 214

A Fourier transform EPR (FT-EPR) study was made of the photochemistry of [Re(R)(CO)3(a-diimine)] and [Ru(E)(R)(CO)2(a-diimine)] complexes, where R " alkyl or benzyl, E " I or SnPh3, and a-diimine " 4,4S-dimethyl-2,2S-bipyridine (DMB) or N,NS-diisopropyl-1,4-diazabutadiene (iPr- DAB). Photoexcitation of these complexes leads to homolysis of the metal-alkyl (benzyl) bonds as evident from the detection of the spectra of the alkyl (benzyl) radicals. FT-EPR spectra display strong spin polarization effects attributed to Triplet Mechanism (TM) and Radical Pair Mechanism (RPM) Chemically Induced Dynamic Electron Polarization (CIDEP). CIDEP patterns point to bond dissociation via a triplet state precursor. For a number of complexes, spin polarization was found to exhibitunusually large solvent effects, whereas for one complex the CIDEP pattern proved to be sensitive to the wavelength of laser light used to initiate bond dissociation. These effects reflect the strong dependence of CIDEP on the character of the excited states involved in the photochemical reactions and contribute to the understanding of the reaction mechanism.