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Efficient Photoinduced Charge Separation in a BODIPY–C60 Dyad
A donor–acceptor dyad composed of a BF2-chelated dipyrromethene (BODIPY) and a C60 fullerene has been newly synthesized and characterized. The two moieties are linked by direct addition of an azido substituted BODIPY on the C60, producing an imino–fullerene–BODIPY adduct. The photoinduced charge tra...
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Published in: | Journal of physical chemistry. C 2016-08, Vol.120 (30), p.16526-16536 |
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container_title | Journal of physical chemistry. C |
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creator | Iagatti, Alessandro Cupellini, Lorenzo Biagiotti, Giacomo Caprasecca, Stefano Fedeli, Stefano Lapini, Andrea Ussano, Eleonora Cicchi, Stefano Foggi, Paolo Marcaccio, Massimo Mennucci, Benedetta Di Donato, Mariangela |
description | A donor–acceptor dyad composed of a BF2-chelated dipyrromethene (BODIPY) and a C60 fullerene has been newly synthesized and characterized. The two moieties are linked by direct addition of an azido substituted BODIPY on the C60, producing an imino–fullerene–BODIPY adduct. The photoinduced charge transfer process in this system was studied by ultrafast transient absorption spectroscopy. Electron transfer toward the fullerene was found to occur selectively exciting both the BODIPY chromophore at 475 nm and the C60 unit at 266 nm on a time scale of a few picoseconds, but the dynamics of charge separation was different in the two cases. Eletrochemical studies provided information on the redox potentials of the involved species and spectroelectrochemical measurements allowed to unambiguously assign the absorption band of the oxidized BODIPY moiety, which helped in the interpretation of the transient absorption spectra. The experimental studies were complemented by a theoretical analysis based on DFT computations of the excited state energies of the two components and their electronic couplings, which allowed identification of the charge transfer mechanism and rationalization of the different kinetic behavior observed by changing the excitation conditions. |
doi_str_mv | 10.1021/acs.jpcc.6b05738 |
format | article |
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C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iagatti, Alessandro</au><au>Cupellini, Lorenzo</au><au>Biagiotti, Giacomo</au><au>Caprasecca, Stefano</au><au>Fedeli, Stefano</au><au>Lapini, Andrea</au><au>Ussano, Eleonora</au><au>Cicchi, Stefano</au><au>Foggi, Paolo</au><au>Marcaccio, Massimo</au><au>Mennucci, Benedetta</au><au>Di Donato, Mariangela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Photoinduced Charge Separation in a BODIPY–C60 Dyad</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2016-08-04</date><risdate>2016</risdate><volume>120</volume><issue>30</issue><spage>16526</spage><epage>16536</epage><pages>16526-16536</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>A donor–acceptor dyad composed of a BF2-chelated dipyrromethene (BODIPY) and a C60 fullerene has been newly synthesized and characterized. The two moieties are linked by direct addition of an azido substituted BODIPY on the C60, producing an imino–fullerene–BODIPY adduct. The photoinduced charge transfer process in this system was studied by ultrafast transient absorption spectroscopy. Electron transfer toward the fullerene was found to occur selectively exciting both the BODIPY chromophore at 475 nm and the C60 unit at 266 nm on a time scale of a few picoseconds, but the dynamics of charge separation was different in the two cases. Eletrochemical studies provided information on the redox potentials of the involved species and spectroelectrochemical measurements allowed to unambiguously assign the absorption band of the oxidized BODIPY moiety, which helped in the interpretation of the transient absorption spectra. The experimental studies were complemented by a theoretical analysis based on DFT computations of the excited state energies of the two components and their electronic couplings, which allowed identification of the charge transfer mechanism and rationalization of the different kinetic behavior observed by changing the excitation conditions.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpcc.6b05738</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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title | Efficient Photoinduced Charge Separation in a BODIPY–C60 Dyad |
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