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Keto-enol tautomerization of 2-(2'-hydroxyphenyl)benzoxazole and 2-(2'-hydroxy-4'-methylphenyl)benzoxazole in the triplet state: Hydrogen tunneling and isotope effects. Transient absorption kinetics.

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Eisenberger,  H.
Department of Spectroscopy and Photochemical Kinetics, MPI for biophysical chemistry, Max Planck Society;

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Nickel,  B.
Department of Spectroscopy and Photochemical Kinetics, MPI for biophysical chemistry, Max Planck Society;

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Ruth,  A. A.
Department of Spectroscopy and Photochemical Kinetics, MPI for biophysical chemistry, Max Planck Society;

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Alsoufi,  W.
Department of Spectroscopy and Photochemical Kinetics, MPI for biophysical chemistry, Max Planck Society;

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Grellmann,  K. H.
Department of Spectroscopy and Photochemical Kinetics, MPI for biophysical chemistry, Max Planck Society;

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Citation

Eisenberger, H., Nickel, B., Ruth, A. A., Alsoufi, W., Grellmann, K. H., & Novo, M. (1991). Keto-enol tautomerization of 2-(2'-hydroxyphenyl)benzoxazole and 2-(2'-hydroxy-4'-methylphenyl)benzoxazole in the triplet state: Hydrogen tunneling and isotope effects. Transient absorption kinetics. Journal of Physical Chemistry, 95(25), 10509-10518.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0013-0ACC-6
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