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The proton-coupled electron-transfer (PCET) reaction is investigated for a newly synthesized imidazole-anthraquinone biomimetic model with a photoactive RuII-polypyridyl moiety that is covalently coupled to the imidazole fragment. Intramolecular H-bonding interactions between imidazole and anthraquinone moieties favor the PCET process; this can be correlated to an appreciable positive shift in the one-electron reduction potential of the coordinated anthraquinone moiety functionalized with the imidazole fragment. This can also be attributed to the low luminescence quantum yield of the RuII-polypyridyl complex used. The dynamics of the intramolecular electron-transfer (ET) and PCET processes are studied by using femtosecond transient absorption spectroscopy. The steady-state spectroscopic studies and the results of the time-resolved absorption studies confirm that H-bonded water molecules play a major role in both ET and PCET dynamics as a proton relay in the excited state. The electron-transfer process is followed by a change in the H-bonding equilibrium between AQ and imidazole in acetonitrile solvent, and protonation of AQ.− by water leads to PCET in the presence of water. A slower forward and backward electron-transfer rate is observed in the presence of D2O compared with that in H2O. These results provide further experimental support for a detailed understanding of the PCET process. [ABSTRACT FROM AUTHOR]