The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes

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Standard

The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes. / Mackeprang, Kasper; Hänninen, Vesa; Halonen, Lauri; Kjærgaard, Henrik Grum.

I: Journal of Chemical Physics, Bind 142, 094304, 2015.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Mackeprang, K, Hänninen, V, Halonen, L & Kjærgaard, HG 2015, 'The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes', Journal of Chemical Physics, bind 142, 094304. https://doi.org/10.1063/1.4913737

APA

Mackeprang, K., Hänninen, V., Halonen, L., & Kjærgaard, H. G. (2015). The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes. Journal of Chemical Physics, 142, [094304]. https://doi.org/10.1063/1.4913737

Vancouver

Mackeprang K, Hänninen V, Halonen L, Kjærgaard HG. The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes. Journal of Chemical Physics. 2015;142. 094304. https://doi.org/10.1063/1.4913737

Author

Mackeprang, Kasper ; Hänninen, Vesa ; Halonen, Lauri ; Kjærgaard, Henrik Grum. / The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes. I: Journal of Chemical Physics. 2015 ; Bind 142.

Bibtex

@article{8567dd40918745fcb7d2a6442854c303,
title = "The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes",
abstract = "We have developed a model to calculate accurately the intensity of the hydrogen bonded XH-stretching vibrational transition in hydrogen bonded complexes. In the Local Mode Perturbation Theory (LMPT) model, the unperturbed system is described by a local mode (LM) model, which is perturbed by the intermolecular modes of the hydrogen bonded system that couple with the intramolecular vibrations of the donor unit through the potential energy surface. We have applied the model to three complexes containing water as the donor unit and different acceptor units, providing a series of increasing complex binding energy: H2O⋯N2, H2O⋯H2O, and H2O⋯NH3. Results obtained by the LMPT model are presented and compared with calculated results obtained by other vibrational models and with previous results from gas-phase and helium-droplet experiments. We find that the LMPT model reduces the oscillator strengths of the fundamental hydrogen bonded OH-stretching transition relative to the simpler LM model.",
author = "Kasper Mackeprang and Vesa H{\"a}nninen and Lauri Halonen and Kj{\ae}rgaard, {Henrik Grum}",
year = "2015",
doi = "10.1063/1.4913737",
language = "English",
volume = "142",
journal = "The Journal of Chemical Physics",
issn = "0021-9606",
publisher = "American Institute of Physics",

}

RIS

TY - JOUR

T1 - The effect of large amplitude motions on the vibrational intensities in hydrogen bonded complexes

AU - Mackeprang, Kasper

AU - Hänninen, Vesa

AU - Halonen, Lauri

AU - Kjærgaard, Henrik Grum

PY - 2015

Y1 - 2015

N2 - We have developed a model to calculate accurately the intensity of the hydrogen bonded XH-stretching vibrational transition in hydrogen bonded complexes. In the Local Mode Perturbation Theory (LMPT) model, the unperturbed system is described by a local mode (LM) model, which is perturbed by the intermolecular modes of the hydrogen bonded system that couple with the intramolecular vibrations of the donor unit through the potential energy surface. We have applied the model to three complexes containing water as the donor unit and different acceptor units, providing a series of increasing complex binding energy: H2O⋯N2, H2O⋯H2O, and H2O⋯NH3. Results obtained by the LMPT model are presented and compared with calculated results obtained by other vibrational models and with previous results from gas-phase and helium-droplet experiments. We find that the LMPT model reduces the oscillator strengths of the fundamental hydrogen bonded OH-stretching transition relative to the simpler LM model.

AB - We have developed a model to calculate accurately the intensity of the hydrogen bonded XH-stretching vibrational transition in hydrogen bonded complexes. In the Local Mode Perturbation Theory (LMPT) model, the unperturbed system is described by a local mode (LM) model, which is perturbed by the intermolecular modes of the hydrogen bonded system that couple with the intramolecular vibrations of the donor unit through the potential energy surface. We have applied the model to three complexes containing water as the donor unit and different acceptor units, providing a series of increasing complex binding energy: H2O⋯N2, H2O⋯H2O, and H2O⋯NH3. Results obtained by the LMPT model are presented and compared with calculated results obtained by other vibrational models and with previous results from gas-phase and helium-droplet experiments. We find that the LMPT model reduces the oscillator strengths of the fundamental hydrogen bonded OH-stretching transition relative to the simpler LM model.

U2 - 10.1063/1.4913737

DO - 10.1063/1.4913737

M3 - Journal article

C2 - 25747078

VL - 142

JO - The Journal of Chemical Physics

JF - The Journal of Chemical Physics

SN - 0021-9606

M1 - 094304

ER -

ID: 132646845