Abstract
The photooxidation of chlorophyll b by 1,4-benzoquinone and 2,6-dimethyl-1,4-benzoquinone was investigated by the technique of chemically-induced dynamic nuclear polarization. Polarization of the proton magnetic resonance lines of the quinone was detected. A mechanism for the photooxidation was postulated that invokes the reaction of the quinone with the excited singlet state of the chlorophyll to form a radical pair. This mechanism, together with a theoretical model and parameters taken from the literature, yields a theoretical proton magnetic resonance spectrum for the polarized quinone that agrees well with that observed experimentally.
Keywords: NMR, excited states, radical pairs
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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
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