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Porphyrin acids
Authors:H. Ogoshi  E. Watanabe  Z. Yoshida
Affiliation:Department of Synthetic Chemistry, Kyoto University, Yoshida, Kyoto 606, Japan
Abstract:The structural change from the porphyrin free base to monoacid and diacid by successive protonation has been studied by the IR, visible and NMR spectroscopy. The results have indicated that the cation and anion of the porphyrin diacid are strongly associated through H-bonding. The far IR spectra show especially marked differences in the free base, monoacid, and diacid due to the changes of the inner core of the porphyrin ring.
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