Electron paramagnetic resonance charge-transfer complex

In a supramolecular approach to fullerene-porphyrin hybrids, the assembly of a rigidly connected dyad, in which a zinc tetraphenylporphyrin, Zn(TPP), is noncovalently linked to a C60 derivative via axial pyridine coordination to the metal, was reported [219-222]. Photo excitation of the dyad Zn-complex led to electron transfer with very long lifetimes of the charge-separated pairs, as revealed by optical spectroscopy and confirmed by time-resolved electron paramagnetic resonance spectroscopy. Accordingly, two different solvent-dependent pathways can be considered for the electron-transfer processes. Either the excitation of the porphyrin chromophore is followed by fast intramolecular electron transfer inside the complex, or alternatively the free porphyrin is excited undergoing intermolecular electron transfer when the acceptor molecules ap-... 

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