Skip navigation

Computational and NMR study of quaternary ammonium ion conformations in solution

Computational and NMR study of quaternary ammonium ion conformations in solution

Luzhkov, Victor B. ORCID: 0000-0003-2521-9968, Osterberg, Fredrik, Acharya, Parag ORCID: 0000-0003-2521-9968, Chattopadhyaya, Jyoti and Agvist, Johan (2002) Computational and NMR study of quaternary ammonium ion conformations in solution. Physical Chemistry Chemical Physics, 4 (19). pp. 4640-4647. ISSN 1463-9076 (Print), 1463-9084 (Online) (doi:https://doi.org/10.1039/b203526j)

Full text not available from this repository. (Request a copy)

Abstract

Conformations around C–N bonds at the quaternary centre in tetraalkylammonium ions in water solution are investigated. Structures of Me4N+, Et4N+, n-Pr4N+, n-Bu4N+, and n-Pe4N+ are calculated using quantum mechanical HF and DFT methods together with the PCM solvent model. Relative solvation free energies of tetraalkylammonium ions are further estimated from microscopic molecular dynamics free energy perturbation simulations using the Gromos-87 and Amber-95 force fields. The predicted free energy difference in solution between two stable conformations of Et4N+, D2d and S4, is 0.6–1.0 kcal mol−1 (in favour of D2d), which is in quantitative agreement with the recent Raman spectroscopy results. The energies of the g+g− conformations of Et4N+ are 3.6–4.0 kcal mol−1 higher. The ions with longer hydrocarbon chains show quite similar energy gap between D2d and S4. The torsion barrier for a two-step interconversion between the D2d and S4 structures is 9.5 kcal mol−1 (HF/6-31G(d) calculations). The computational results are augmented by NMR measurements of the Et4N+–I− salt in aqueous solution, which predict a symmetric structure of Et4N+ in water. However, the D2d and S4 conformers are not discernible due to presumably high similarity of chemical shifts. The calculated conformational energetics in solution together with previously observed D2d, S4 and high-energy g+g−-type structures of Et4N+, n-Pr4N+, and n-Bu4N+ in the solid state indicate that the carbon chain conformations at the quaternary ammonium centre sensitively depend on the actual microenvironment.

Item Type: Article
Uncontrolled Keywords: computational study, NMR, conformation
Subjects: Q Science > Q Science (General)
Faculty / Department / Research Group: Faculty of Engineering & Science
Faculty of Engineering & Science > Natural Resources Institute
Faculty of Engineering & Science > Natural Resources Institute > Food & Markets Department
Last Modified: 08 Jul 2020 14:25
Selected for GREAT 2016: None
Selected for GREAT 2017: None
Selected for GREAT 2018: None
Selected for GREAT 2019: None
Selected for REF2021: None
URI: http://gala.gre.ac.uk/id/eprint/28727

Actions (login required)

View Item View Item