| Institution: | 1. Institute for Physical and Theoretical Chemistry, Goethe University Frankfurt/Main, Max-von-Laue-Str. 7, 60438 Frankfurt/Main, Germany;2. Current address: Department of Chemistry, Science Institute, University of Iceland, Dunhaga 3, Reykjavik, postcode is missing Iceland
Institute for Organic Chemistry and Chemical Biology, Goethe University Frankfurt/Main, Max-von-Laue-Str. 7, 60438 Frankfurt/Main, Germany;3. Institute for Organic Chemistry and Chemical Biology, Goethe University Frankfurt/Main, Max-von-Laue-Str. 7, 60438 Frankfurt/Main, Germany |
| Abstract: | Photoacids attract increasing scientific attention, as they are valuable tools to spatiotemporally control proton-release reactions and pH values of solutions. We present the first time-resolved spectroscopic study of the excited state and proton-release dynamics of prominent merocyanine representatives. Femtosecond transient absorption measurements of a pyridine merocyanine with two distinct protonation sites revealed dissimilar proton-release mechanisms: one site acts as a photoacid generator as its pKa value is modulated in the ground state after photoisomerization, while the other functions as an excited state photoacid which releases its proton within 1.1 ps. With a pKa drop of 8.7 units to ?5.5 upon excitation, the latter phenolic site is regarded a super-photoacid. The 6-nitro derivative exhibits only a phenolic site with similar, yet slightly less photoacidic characteristics and both compounds transfer their proton to methanol and ethanol. In contrast, for the related 6,8-dinitro compound an intramolecular proton transfer to the ortho-nitro group is suggested that is involved in a rapid relaxation into the ground state. |
