The Journal of Organic Chemistry · 2001 · 57 citations · 25 references
Natural SciencesChemistryMaterials ScienceElectroanalytical MethodsElectrochemical EngineeringOrganic ChemistryMicrowave-assisted SynthesisOrganic SemiconductorsPhotochemical KineticsPhotochemistryPhotoelectrochemical MaterialsPhotoelectrochemistry1, 3-Dipolar CycloadditionCycloaddition ReactionsElectrochemical FunctionalizationMicrowave Irradiation EffectsMicrowave-assisted Organic SynthesisPhotoinduced Charge TransferTime-resolved Fluorescence Spectroscopy
A series of triad pyrazolylpyrazolino[60]fullerenes has been prepared in one pot from suitably functionalized hydrazones by 1,3-dipolar cycloaddition reactions under microwave irradiation. The electrochemical properties of the compounds obtained were investigated by cyclic voltammmetry, and they show better electron acceptor character than the parent C(60) in all cases. Fluorescence experiments and time-resolved transition spectroscopy indicate the existence of photoinduced charge-transfer processes with the C(60) triplet acting as the acceptor.
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