Efficient electron transfer in β-substituted porphyrin-C60 dyads connected through a p-phenylenevinylene dimer

Two new porphyrin-C60 dyads have been synthesized in which the electroactive moieties have been connected through a p-phenylenevinylene dimer. The electrochemical study confirms the amphoteric redox behavior of these dyads. Irradiation of these compounds gives rise to the corresponding radical pair confirming that substitution on the β-position of the porphyrin facilitates the electronic communication between the porphyrin and C60.

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