Abstract
Solvent polarity effects on the energetics of charge separation processes, in particular on proton transfer in 1-morpholinomethyl-2-naphthol (M2N), were studied and discussed in the frame of a continuum model. The obtained results were compared to electron transfer (TICT) inp-cyano-N,N-dimethylaniline (CDMA). Solvatochromic shifts of M2N were explained by an increase of the molecular dipole moment on excitation, but more importantly by a rotation of its direction. A minimum in the excited state lifetime in an intermediate polarity region was attributed to a maximum radiationless transition probability.
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Köhler, G., Wolschann, P. & Rotkiewicz, K. Solvent effects on intramolecular charge separation. Proc. Indian Acad. Sci. (Chem. Sci.) 104, 197–207 (1992). https://doi.org/10.1007/BF02863364
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DOI: https://doi.org/10.1007/BF02863364