Exploring Nature and Predicting Strength of Hydrogen Bonds: A Correlation Analysis Between Atoms-in-Molecules Descriptors, Binding Energies, and Energy Components of Symmetry-Adapted Perturbation Theory

0518316 - BFÚ 2020 RIV US eng J - Článek v odborném periodiku
Emamian, S. - Lu, T. - Kruse, Holger - Emamian, H.
Exploring Nature and Predicting Strength of Hydrogen Bonds: A Correlation Analysis Between Atoms-in-Molecules Descriptors, Binding Energies, and Energy Components of Symmetry-Adapted Perturbation Theory.
Journal of Computational Chemistry. Roč. 40, č. 32 (2019), s. 2868-2881. ISSN 0192-8651. E-ISSN 1096-987X
Institucionální podpora: RVO:68081707
Klíčová slova: gaussian-basis sets * electron-density * wave-function * qtaim * localization
Obor OECD: Organic chemistry
Impakt faktor: 2.976, rok: 2019
Způsob publikování: Omezený přístup
https://onlinelibrary.wiley.com/doi/full/10.1002/jcc.26068

This work studies the underlying nature of H-bonds (HBs) of different types and strengths and tries to predict binding energies (BEs) based on the properties derived from wave function analysis. A total of 42 HB complexes constructed from 28 neutral and 14 charged monomers were considered. This set was designed to sample a wide range of HB strengths to obtain a complete view about HBs. BEs were derived with the accurate coupled cluster singles and doubles with perturbative triples correction (CCSD(T))(T) method and the physical components of the BE were investigated by symmetry-adapted perturbation theory (SAPT). Quantum theory of atoms-in-molecules (QTAIM) descriptors and other HB indices were calculated based on high-quality density functional theory wave functions. We propose a new and rigorous classification of H-bonds (HBs) based on the SAPT decomposition. Neutral complexes are either classified as 'very weak' HBs with a BE >=2.5 kcal/mol that are mainly dominated by both dispersion and electrostatic interactions or as 'weak-to-medium' HBs with a BE varying between2.5 and14.0 kcal/mol that are only dominated by electrostatic interactions. On the other hand, charged complexes are divided into 'medium' HBs with a BE in the range of11.0 to15.0 kcal/mol, which are mainly dominated by electrostatic interactions, or into 'strong' HBs whose BE is more negative than15.0 kcal/mol, which are mainly dominated by electrostatic together with induction interactions. Among various explored correlations between BEs and wave function-based HB descriptors, a fairly satisfactory correlation was found for the electron density at the bond critical point (BCP, rho(BCP)) of HBs. The fitted equation for neutral complexes is BE/kcal/mol = 223.08 x rho(BCP)/a. u. + 0.7423 with a mean absolute percentage error (MAPE) of 14.7%, while that for charged complexes is BE/kcal/mol = 332.34 x rho(BCP)/a. u. 1.0661 with a MAPE of 10.0%. In practice, these equations may be used for a quick estimation of HB BEs, for example, for intramolecular HBs or large HB networks in biomolecules. (c) 2019 Wiley Periodicals, Inc.
Trvalý link: http://hdl.handle.net/11104/0303478