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| Title
| - Control of Photoinduced Electron Transfer in Zinc Phthalocyanine−Perylenediimide Dyad and Triad by the Magnesium Ion
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| Abstract
| - Photoexcitation of a zinc phthalocyanine−perylenediimide (ZnPc−PDI) dyad and a bis(zinc phthalocyanine)−perylenediimide [(ZnPc)2−PDI] triad results in formation of the triplet excited state of the PDI moiety without the fluorescence emission, whereas addition of Mg2+ ions to the dyad and triad results in formation of long-lived charge-separated (CS) states (ZnPc•+−PDI•−/Mg2+ and (ZnPc)2•+−PDI•−/Mg2+) in which PDI•− forms a complex with Mg2+. Formation of the CS states in the presence of Mg2+ was confirmed by appearance of the absorption bands due to ZnPc•+ and PDI•−/Mg2+ complex in the time-resolved transient absorption spectra of the dyad and triad. The one-electron reduction potential (Ered) of the PDI moiety in the presence of a metal ion is shifted to a positive direction due to the binding of Mg2+ to PDI•−, whereas the one-electron oxidation potential of the ZnPc moiety remains the same. The binding of Mg2+ to PDI•− was confirmed by the ESR spectrum, which is different from that of PDI•− without Mg2+. The energy of the CS state (ZnPc•+−PDI•−/Mg2+) is determined to be 0.79 eV, which becomes lower that of the triplet excited state (ZnPc−3PDI*: 1.07 eV). This is the reason why the long-lived CS states were attained in the presence of Mg2+ instead of the triplet excited state of the PDI moiety.
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| - Electron Transfer in ZnPc−PDI
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