Tikhonov, Denis S.Scutelnic, ValeriuSharapa, Dmitry, IKrotova, Alina A.Dmitrieva, Alena, VObenchain, Daniel A.Schnell, Melanie2022-10-242022-10-242022-10-24202310.1007/s11224-022-02053-4https://infoscience.epfl.ch/handle/20.500.14299/191612WOS:000864322000001Here, we present new cryogenic infrared spectra of the (Imidazole) H-n(+) (n=1,2,3) ions. The data was obtained using helium tagging infrared predissociation spectroscopy. The new results were compared with the data obtained by Gerardi et al. (Chem. Phys. Lett. 501:172-178, 2011) using the same technique but with argon as a tag. Comparison of the two experiments, assisted by theoretical calculations, allowed us to evaluate the preferable attachment positions of argon to the (Imidazole) nH+ frame. Argon attaches to nitrogen-bonded hydrogen in the case of the (Imidazole)H+ ion, while in (Imidazole)(2)H+ and (Imidazole)(3)H+ the preferred docking sites for the argon are in the center of the complex. This conclusion is supported by analyzing the spectral features attributed to the N-H stretching vibrations. Symmetry adapted perturbation theory (SAPT) analysis of the non-covalent forces between argon and the (Imidazole)(n)H+ (n=1,2,3) frame revealed that this switch of docking preference with increasing complex size is caused by an interplay between induction and dispersion interactions.Chemistry, MultidisciplinaryChemistry, PhysicalCrystallographyChemistryprotonated imidazole clustersinert gas atomsir spectroscopytag spectroscopysaptbiomolecular building-blocksdensity-functional theoryorbital coupled-clusterbasis-setsvibrational-spectraperturbation-theoryimidazoleenergiesefficientdynamicstext::journal::journal article::research article