Photoelectron spectroscopy and ab initio calculations employing a nonequilibrium polarizable continuum model were employed for determining the vertical ionization potential of aqueous protonated imidazole. The experimental value of 8.96 eV is in in excellent agreement with calculations, which also perform quantitatively for ionization of aqueous alkali cations as benchmark species. The present results show that protonation of imidazole increases its vertical ionization potential up in water by 0.7 eV, which is significantly larger than the resolution of the experiment or the error of the calculation. This combined experimental and computational approach may open the possibility for quantitatively analyzing the protonation state of histidine, of which imidazole is the titratable side chain group, in aqueous peptides and proteins.

Institute of Organic Chemistry and Biochemistry Academy of Sciences of the Czech Republic and Center for Complex Molecular Systems and Biomolecules Flemingovo nám 2 16610 Prague 6 Czech Republic

Citace poskytuje Crossref.org

Following in Emil Fischer's Footsteps: A Site-Selective Probe of Glucose Acid-Base Chemistry