<scp>Gas‐phase</scp> thermochemistry of noncovalent ligand–alkali metal ion clusters: An impact of low frequencies
Arseniy A. Otlyotov, Yury Minenkov
Abstract
Abstract The experimental gas‐phase thermochemistry of reactions: M + (S) n –1 + S → M + (S) n and M + + n S→ M + (S) n , where M is an alkali metal and S is acetonitrile/ammonia, is reproduced. Three approximations are tested: (1) scaled rigid‐rotor‐harmonic‐oscillator (sRRHO); (2) the sRRHO(100) identical to (1), but with all vibrational frequencies smaller than 100 cm −1 replaced with 100 cm −1 ; (3) Grimme's modified scaled RRHO (msRRHO) (Grimme, Chem. Eur. J. , 2012, 18, 9955–9964). The msRRHO approach provides the most accurate reaction entropies with the mean unsigned error (MUE) below 5.5 cal mol −1 K −1 followed by sRRHO(100) and sRRHO with MUEs of 7.2 and 16.9 cal mol −1 K −1 . For the first time, we propose using the msRRHO scheme to calculate the enthalpy contribution that is further utilized to arrive at reaction Gibbs free energies (∆G r ) ensuring the internal consistency. The final ∆G r MUEs for msRRHO, sRRHO(100) and sRRHO schemes are 1.2, 3.6 and 3.1 kcal mol −1 .