Dimerization of Acetic Acid in the Gas Phase—NMR Experiments and Quantum-Chemical Calculations

0524556 - ÚOCHB 2021 RIV CH eng J - Článek v odborném periodiku
Socha, Ondřej - Dračínský, Martin
Dimerization of Acetic Acid in the Gas Phase—NMR Experiments and Quantum-Chemical Calculations.
Molecules. Roč. 25, č. 9 (2020), č. článku 2150. E-ISSN 1420-3049
Grant CEP: GA ČR(CZ) GA20-01472S
Institucionální podpora: RVO:61388963
Klíčová slova: NMR spectroscopy * quantum-chemical calculations * phase transitions * carboxylic acids * hydrogen bonding
Obor OECD: Physical chemistry
Impakt faktor: 4.412, rok: 2020
Způsob publikování: Open access
https://www.mdpi.com/1420-3049/25/9/2150

Due to the nature of the carboxylic group, acetic acid can serve as both a donor and acceptor of a hydrogen bond. Gaseous acetic acid is known to form cyclic dimers with two strong hydrogen bonds. However, trimeric and various oligomeric structures have also been hypothesized to exist in both the gas and liquid phases of acetic acid. In this work, a combination of gas-phase NMR experiments and advanced computational approaches were employed in order to validate the basic dimerization model of gaseous acetic acid. The gas-phase experiments performed in a glass tube revealed interactions of acetic acid with the glass surface. On the other hand, variable-temperature and variable-pressure NMR parameters obtained for acetic acid in a polymer insert provided thermodynamic parameters that were in excellent agreement with the MP2 (the second order Møller–Plesset perturbation theory) and CCSD(T) (coupled cluster with single, double and perturbative triple excitation) calculations based on the basic dimerization model. A slight disparity between the theoretical dimerization model and the experimental data was revealed only at low temperatures. This observation might indicate the presence of other, entropically disfavored, supramolecular structures at low temperatures.
Trvalý link: http://hdl.handle.net/11104/0308898