Electron Transfer and Multi‐Electron Accumulation in ExBox4+ |
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Authors: | Scott M. Dyar Jonathan C. Barnes Dr. Michal Juríček Prof. J. Fraser Stoddart Prof. Dick T. Co Prof. Ryan M. Young Prof. Michael R. Wasielewski |
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Affiliation: | 1. Department of Chemistry, Northwestern University (USA);2. Department of Chemistry, University Basel, St. Johanns‐Ring 19, 4056 Basel (Switzerland);3. Argonne‐Northwestern Solar Energy Research (ANSER) Center, 2145 Sheridan Road, Evanston, IL 60208 (USA) |
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Abstract: | Molecules capable of accepting and storing multiple electrons are crucial components of artificial photosynthetic systems designed to drive catalysts, such as those used to reduce protons to hydrogen. ExBox4+, a boxlike cyclophane comprising two π‐electron‐poor extended viologen units tethered at both ends by two p‐xylylene linkers, has been shown previously to accept an electron through space from a photoexcited guest. Herein is an investigation of an alternate, through‐bond intramolecular electron‐transfer pathway involving ExBox4+ using a combination of transient absorption and femtosecond stimulated Raman spectroscopy (FSRS). Upon photoexcitation of ExBox4+, an electron is transferred from one of the p‐xylylene linkers to one of the extended viologen units in ca. 240 ps and recombines in ca. 4 ns. A crystal structure of the doubly reduced species ExBox2+ was obtained. |
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Keywords: | cyclophanes electron transfer ExBox femtochemistry photochemistry |
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