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- W1494996535 endingPage "2001" @default.
- W1494996535 startingPage "1984" @default.
- W1494996535 abstract "Abstract Porphyrin amino acids 3a – 3h with meso substituents Ar of tunable electron‐donating power (Ar = 4‐C 6 H 4 O n Bu, 4‐C 6 H 4 OMe, 4‐C 6 H 4 Me, Mes, C 6 H 5 , 4‐C 6 H 4 F, 4‐C 6 H 4 CF 3 , C 6 F 5 ) have been linked at the N terminus to anthraquinone Q as electron acceptor through amide bonds to give Q‐P Ar dyads 4a – 4h . These were conjugated to ferrocene Fc at the C terminus as electron donor to give the acceptor‐chromophore‐donor Q‐P Ar ‐Fc triads 6a – 6h . To further modify the energies of the electronically excited and charge‐separated states, the triads 6a – 6h were metallated with zinc(II) to give the corresponding Q‐(Zn)P Ar ‐Fc triads Zn‐6a – Zn‐6h . The Q‐P Ar1 dyad (Ar 1 = C 6 H 5 ) was further extended with a second porphyrin P Ar2 (Ar 2 = 4‐C 6 H 4 Me) as well as appended to a ferrocene to give the tetrad Q‐P Ar1 ‐P Ar2 ‐Fc 9 . Almost all the conjugates show strongly reduced fluorescence quantum yields and excited‐state lifetimes, which has been interpreted as photoinduced electron transfer (PET) either from the excited porphyrin to the quinone (oxidative PET) or from the ferrocene to the excited porphyrin (reductive PET). Electrochemical data, absorption spectroscopy, steady‐state emission, time‐resolved fluorescence, transient absorption pump‐probe spectroscopy as well as DFT calculations have been used to elaborate the preferred PET pathway (reductive vs. oxidative PET) in these architectures with systematically varied electron‐donating substituents at the central chromophore." @default.
- W1494996535 created "2016-06-24" @default.
- W1494996535 creator A5011496890 @default.
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- W1494996535 creator A5040695029 @default.
- W1494996535 creator A5077044863 @default.
- W1494996535 creator A5087130957 @default.
- W1494996535 date "2014-02-27" @default.
- W1494996535 modified "2023-10-10" @default.
- W1494996535 title "Tuning Reductive and Oxidative Photoinduced Electron Transfer in Amide‐Linked Anthraquinone–Porphyrin–Ferrocene Architectures" @default.
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- W1494996535 doi "https://doi.org/10.1002/ejic.201400118" @default.