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An alkynyl\u2013fullerene synthon was synthesized by a nucleophilic addition reaction, and was then oxidatively coupled with a series of alkynyl tetra\u2010aryl zinc\u2013porphyrins with 1\u20133 alkyne units. Cyclic and differential pulse voltammetry studies confirmed that the porphyrin and fullerene are electronically coupled and that the degree of electronic interaction decreases with increasing length of the alkyne bridge. In toluene, energy transfer from the excited zinc\u2013porphyrin singlet to the fullerene moiety occurs, affording fullerene triplet quantum yields of greater than 90\u2009%. These dyads exhibit very rapid photoinduced electron transfer in tetrahydrofuran (THF) and benzonitrile (PhCN), which is consistent with normal Marcus behavior. Slower rates for charge recombination in THF versus PhCN clearly indicate that charge\u2010recombination events are occurring in the Marcus inverted region. Exceptionally small attenuation factors (<jats:italic>\u03b2<\/jats:italic>) of 0.06\u00b10.005 \u00c5<jats:sup>\u22121<\/jats:sup> demonstrate that the triple bond is an effective mediator of electronic interaction in zinc\u2013porphyrin\u2013alkyne\u2013fullerene molecular wires.<\/jats:p>","DOI":"10.1002\/chem.200401348","type":"journal-article","created":{"date-parts":[[2005,3,31]],"date-time":"2005-03-31T10:25:24Z","timestamp":1112264724000},"page":"3375-3388","source":"Crossref","is-referenced-by-count":110,"title":["Energy and Electron Transfer in Polyacetylene\u2010Linked Zinc\u2013Porphyrin\u2013[60]Fullerene Molecular Wires"],"prefix":"10.1002","volume":"11","author":[{"given":"Sean A.","family":"Vail","sequence":"first","affiliation":[]},{"given":"Paul J.","family":"Krawczuk","sequence":"additional","affiliation":[]},{"given":"Dirk M.","family":"Guldi","sequence":"additional","affiliation":[]},{"given":"Amit","family":"Palkar","sequence":"additional","affiliation":[]},{"given":"Luis","family":"Echegoyen","sequence":"additional","affiliation":[]},{"given":"Joao P. 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