Gauge-origin independent magnetizabilities from hybrid quantum mechanics/molecular mechanics models: Theory and applications to liquid water
(2007) In Chemical Physics Letters 442(4-6). p.322-328- Abstract
- The theory of a hybrid quantum mechanics/molecular mechanics (QM/MM) approach for gauge-origin independent calculations of the molecular magnetizability using Hartree-Fock or Density Functional Theory is presented. The method is applied to liquid water using configurations generated from classical Molecular Dynamics simulation to calculate the statistical averaged magnetizability. Based on a comparison with experimental data, treating only one water molecule quantum mechanically appears to be insufficient, while a quantum mechanical treatment of also the first solvation shell leads to good agreement between theory and experiment. This indicates that the gas-to-liquid phase shift for the molecular magnetizability is to a large extent of... (More)
- The theory of a hybrid quantum mechanics/molecular mechanics (QM/MM) approach for gauge-origin independent calculations of the molecular magnetizability using Hartree-Fock or Density Functional Theory is presented. The method is applied to liquid water using configurations generated from classical Molecular Dynamics simulation to calculate the statistical averaged magnetizability. Based on a comparison with experimental data, treating only one water molecule quantum mechanically appears to be insufficient, while a quantum mechanical treatment of also the first solvation shell leads to good agreement between theory and experiment. This indicates that the gas-to-liquid phase shift for the molecular magnetizability is to a large extent of non-electrostatic nature. (c) 2007 Elsevier B.V. All rights reserved. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/648141
- author
- Aidas, Kestutis ; Kongsted, Jacob LU ; Nielsen, Christian B. ; Mikkelsen, Kurt V. ; Christiansen, Ove and Ruud, Kenneth
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Chemical Physics Letters
- volume
- 442
- issue
- 4-6
- pages
- 322 - 328
- publisher
- Elsevier
- external identifiers
-
- wos:000248382300030
- scopus:34347327058
- ISSN
- 0009-2614
- DOI
- 10.1016/j.cplett.2007.06.003
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Theoretical Chemistry (S) (011001039)
- id
- e8533438-29e3-4ba9-9d44-a4fb71ffbb71 (old id 648141)
- date added to LUP
- 2016-04-01 16:13:08
- date last changed
- 2023-01-04 22:09:40
@article{e8533438-29e3-4ba9-9d44-a4fb71ffbb71, abstract = {{The theory of a hybrid quantum mechanics/molecular mechanics (QM/MM) approach for gauge-origin independent calculations of the molecular magnetizability using Hartree-Fock or Density Functional Theory is presented. The method is applied to liquid water using configurations generated from classical Molecular Dynamics simulation to calculate the statistical averaged magnetizability. Based on a comparison with experimental data, treating only one water molecule quantum mechanically appears to be insufficient, while a quantum mechanical treatment of also the first solvation shell leads to good agreement between theory and experiment. This indicates that the gas-to-liquid phase shift for the molecular magnetizability is to a large extent of non-electrostatic nature. (c) 2007 Elsevier B.V. All rights reserved.}}, author = {{Aidas, Kestutis and Kongsted, Jacob and Nielsen, Christian B. and Mikkelsen, Kurt V. and Christiansen, Ove and Ruud, Kenneth}}, issn = {{0009-2614}}, language = {{eng}}, number = {{4-6}}, pages = {{322--328}}, publisher = {{Elsevier}}, series = {{Chemical Physics Letters}}, title = {{Gauge-origin independent magnetizabilities from hybrid quantum mechanics/molecular mechanics models: Theory and applications to liquid water}}, url = {{http://dx.doi.org/10.1016/j.cplett.2007.06.003}}, doi = {{10.1016/j.cplett.2007.06.003}}, volume = {{442}}, year = {{2007}}, }