Synthesis of tetrathiafulvalene by photoinduced electron-transfer reactions.

Dynamics of Bimolecular Photoinduced Electron-Transfer Reactions

From the accumulated results of several research groups over the last 25 years, it is clear that photoinduced electron-transfer reactions have significantly broadened the scope of organic photochemistry.1 The fundamental mechanistic principle is that when quenching of an excited state via electron transfer is sufficiently exothermic, the reaction occurs at or close to the diffusion-controlled l...

ultrafast spectroscopy on bimolecular photoinduced electron transfer reactions

in Figure 1. After excitation of one of the reactants, diffusion is required to bring the reaction partners at distances where charge separation (CS) can occur. The nature of the primary quenching product is still debated.3 For weakly exergonic CS, ∆GCS > ~ -0.4 eV, it is generally accepted that the product is a contact ion pair (CIP), that is, two ions at a distance enabling a substantial over...

Nonequilibrium photoinduced electron transfer

Polythiophene derivatives by step-growth polymerization via photoinduced electron transfer reactions.

A novel method for the step-growth polymerization of diphenyldithienothiophene in the presence of diphenyliodonium salt by photoinduced electron transfer is described.

Photoinduced electron transfer in a supramolecular triad produced by porphyrin anion-induced electron transfer from tetrathiafulvalene calix[4]pyrrole to Li(+)@C60.

Binding of a porphyrin carboxylate anion () to tetrathiafulvalene calix[4]pyrrole (TTF-C4P) results in electron transfer from TTF-C4P to Li(+)@C60 to produce the charge-separated state (1/TTF-C4P˙(+)/Li(+)@C60˙(-)) in benzonitrile. Upon photoexcitation of , photoinduced electron transfer from the triplet excited state of to TTF-C4P˙(+) occurs to produce the higher energy charge-separated state ...