Abstract
The mechanism of proton-assisted photoinduced electron transfer from porphyrins to quinones has been investigated by a combination of NMR, photo-CIDNP, laser flash photolysis, and UV-vis absorption techniques. In aromatic solvents containing trifluoroacetic acid, the electron-donor species was found to be the triplet state of the porphyrin dication rather than that of the free-base porphyrin itself. In addition, reaction of the porphyrin dication triplet state with the protonated quinone species QH+, rather than Q, was found to be responsible for the observed electron transfer and the resulting CIDNP signals.
Original language | English (US) |
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Pages (from-to) | 4442-4445 |
Number of pages | 4 |
Journal | Journal of physical chemistry |
Volume | 95 |
Issue number | 11 |
DOIs | |
State | Published - 1991 |
ASJC Scopus subject areas
- Engineering(all)
- Physical and Theoretical Chemistry