Ultrafast dynamics of the ESIPT photoswitch N-(3-pyridinyl)-2-pyridinecarboxamideElectronic supplementary information (ESI) available: Crystal structure data; calculated ground state structures for I and IV; calculated excitation energies and UV spectra; TEAS time profiles for NPPCA in water; decay-associated spectra from singular value decomposition analyses; comparison of experimental and calculated vibrational spectra; comparison of a late-time TVA spectrum to calculated vibrational spectra f

• Main Authors: Böhnke, Hendrik, Bahrenburg, Julia, Ma, Xiaonan, Röttger, Katharina, Näther, Christian, Rode, Micha F, Sobolewski, Andrzej L, Temps, Friedrich
• Format: Article
• Language: English
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c7cp06145e

Molecular switches based on proton transfer that are photochromic and can be interconverted by light at different wavelengths back and forth between two thermodynamically stable tautomeric states in solution at room temperature are rare to date. We report on a study of the ultrafast conversion of the bistable proton transfer switch N -(3-pyridinyl)-2-pyridinecarboxamide (NPPCA) to a corresponding iminol after photoexcitation at λ pump 265 nm by means of femtosecond time-resolved broad-band and single-colour transient electronic absorption spectroscopy (TEAS), transient fluorescence spectroscopy (TFLS), and transient vibrational absorption spectroscopy (TVAS) in acetonitrile solution. The interpretation of the data was accompanied by ab initio quantum chemical calculations of the excited electronic states and the vibrational frequencies of the reactant and product in their ground electronic state. The TEAS experiments provided four time constants, τ 1 = 0.09 ± 0.01 ps, τ 2 = 0.61 ± 0.01 ps, τ 3 = 5.10 ± 0.80 ps, and τ 4 = 20.0 ± 1.0 ps. The first two agree well with the measured TFLS lifetimes, τ 1,TFL < 0.18 ps and τ 2,TFL = 0.50 ± 0.01 ps. τ 1 is related to the relaxation of the initially excited Franck-Condon (FC) state of the pyridinecarboxamide, followed by the excited-state intramolecular proton transfer (ESIPT) step to the neighbouring pyridine. The subsequent return of the molecules to the electronic ground state takes place within τ 2 , mediated by a conical intersection (CI) at a twisted configuration of the pyridinecarboxamide moiety. The main components in all TEAS time profiles feature a rise with τ 2 and a decay with τ 4 and describe subsequent molecular transformations in the electronic ground state. τ 3 is ascribed to vibrational cooling of the molecules. The final iminol exhibits a permanent UV absorption at λ = 247 nm, where its absorbance is stronger than that of the carboxamide reactant. The iminol structure is unambiguously identified by the TVA spectra, which show the build-up of corresponding vibrational bands with τ 4,TVA = 23 ± 2 ps after the initial bleach of the reactant vibrational bands, in excellent agreement with the TEAS data. Its lifetime is >10 ns. A potential ESIPT photoswitch has been investigated by femtosecond time-resolved electronic and vibrational absorption spectroscopy.