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Université de Fribourg

The Primary steps in excited-state hydrogen transfer: the phototautomerization of o-nitrobenzyl derivatives

Šolomek, Tomáš ; Bochet, Christian G. ; Bally, Thomas

In: Chemistry – A European Journal, 2014, vol. 20, no. 26, p. 8062–8067

The quantum yield for the release of leaving groups from o-nitrobenzyl “caged” compounds varies greatly with the nature of these leaving groups, for reasons that have never been well understood. We found that the barriers for the primary hydrogen-atom transfer step and the efficient nonradiative processes on the excited singlet and triplet surfaces determine the quantum yields. The...

Université de Fribourg

Oxidative rearrangements of tricyclic vinylcyclobutane derivatives

Grota, Juliane ; Mattay, Jochen ; Piech, Krzysztof ; Bally, Thomas

In: Chemistry - A European Journal, 2006, vol. 12(17), p. 4559-4567

Three tricyclic vinylcyclobutanes (3-methylenetricyclo[5.3.0.02,6]decanes 1-3) have been subjected to ionization by photoinduced electron transfer in solution and by X-irradiation in Ar matrices. All three compounds undergo oxidative cycloreversion; the cleavage of the four-membered ring, however, occurs in a different direction depending on the presence of a methyl group...