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Karl Heinz Grellmann - Publications

Affiliations: 
Max-Planck-Institut für biophysikalische Chemie, Göttingen, Göttingen, Niedersachsen, Germany 
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6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
1994 Stephan JS, Rodríguez CR, Grellmann KH, Zachariasse KA. Flash-photolysis of 2-(2'-hydroxyphenyl)-3-H-indole. Ground-state keto-enol tautomerization by mutual hydrogen exchange and by proton catalysis Chemical Physics. 186: 435-446. DOI: 10.1016/0301-0104(94)01624-0  0.46
1994 Stephan JS, Mordziński A, Rodríguez CR, Grellmann KH. Photoisomerizations of the photochromic anil salicylidene-1-naphthylamine in 3-methylpentane Chemical Physics Letters. 229: 541-550. DOI: 10.1016/0009-2614(94)01078-1  0.53
1991 Al-Soufi W, Grellmann KH, Nickel B. Keto-Enol Tautomerization of 2-(2'-Hydroxyphenyl) benzoxazole and 2-(2'-Hydroxy-4'-methylphenyl) benzoxazole in the Triplet State: Hydrogen Tunneling and Isotope Effects. 2. Dual Phosphorescence Kinetics The Journal of Physical Chemistry. 95: 10503-10509. DOI: 10.1021/J100178A044  0.486
1990 Al-Soufi W, Grellmann KH, Nickel B. Triplet state formation and cis→ trans isomerization in the excited singlet state of the keto tautomer of 2-(2'-hydroxyphenyl) benzothiazole Chemical Physics Letters. 174: 609-616. DOI: 10.1016/0009-2614(90)85495-X  0.481
1988 Prieto MFR, Nickel B, Grellmann KH, Mordziński A. Dual phosphorescence from 2-(2′-hydroxyphenyl)benzoxazole due to keto-enol tautomerism in the metastable triplet state Chemical Physics Letters. 146: 387-392. DOI: 10.1016/0009-2614(88)87464-5  0.407
1985 Bartelt G, Eychmüller A, Grellmann KH. Experimental studies of hydrogen tunnelling. Utilization of large isotope effects in a mechanistic study of a hydrogen shift reaction. Chemical Physics Letters. 118: 568-572. DOI: 10.1016/0009-2614(85)85355-0  0.467
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