Synthesis, Photophysical and Electochemical Properties of Amide-bridged Porphyrin-Anthraquinone Dimers
Corresponding Author(s) : Wei Li
zhouxueqin@tju.edu.cn; liulizeng@126.com
Asian Journal of Chemistry,
Vol. 24 No. 8 (2012): Vol 24 Issue 8
Abstract
Photoinduced electron-transfer processes of two newly synthesized porphyrin-anthraquinone dyads bridged with amide were studied with the UV-visible, fluorescence and transient absorption spectra. Results indicated that the intramolecular electron-transfer might take place via the excited states of the 5-(4-carboxyphenyl)-10,15,20-triphenylporphyrin unit to the anthraquinone moiety.
Keywords
Porphyrin
Anthraquinone
Electron transfer
Dyads
Synthesis
Liu, L.-Z., Liu, D.-Z., Tao, M.-L., Zhou, X.-Q., & Li, W. (2012). Synthesis, Photophysical and Electochemical Properties of Amide-bridged Porphyrin-Anthraquinone Dimers. Asian Journal of Chemistry, 24(8), 3490–3492. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/9422
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