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Deciphering the infrared spectrum of the protonated water pentamer and the hybrid Eigen-Zundel cation

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Deciphering the infrared spectrum of the protonated water pentamer and the hybrid Eigen-Zundel cation. / Kulig, Waldemar; Agmon, Noam.

In: Physical Chemistry Chemical Physics, Vol. 16, No. 10, 14.03.2014, p. 4933-4941.

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Kulig, W & Agmon, N 2014, 'Deciphering the infrared spectrum of the protonated water pentamer and the hybrid Eigen-Zundel cation', Physical Chemistry Chemical Physics, vol. 16, no. 10, pp. 4933-4941. https://doi.org/10.1039/c3cp54029d

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Kulig, Waldemar ; Agmon, Noam. / Deciphering the infrared spectrum of the protonated water pentamer and the hybrid Eigen-Zundel cation. In: Physical Chemistry Chemical Physics. 2014 ; Vol. 16, No. 10. pp. 4933-4941.

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@article{4f191ea8a7ea45f29a446d51caf0dc3d,
title = "Deciphering the infrared spectrum of the protonated water pentamer and the hybrid Eigen-Zundel cation",
abstract = "Traditionally, infrared band assignment for the protonated water clusters, such as H+(H2O)5, is based on their lowest energy isomer. Recent experiments extend the observation spectral window to lower frequencies, for which such assignment appears to be inadequate. Because this hydrogen-bonded system is highly anharmonic, harmonic spectral calculations are insufficient for reliable interpretation. Consequently, we have calculated the IR spectrum of several isomers of the protonated water pentamer using an inherently anharmonic methodology, utilizing dipole and velocity autocorrelation functions computed from ab initio molecular dynamic trajectories. While the spectrum of H+(H2O)5 is universally assumed to represent the branched Eigen isomer, we find a better agreement for a mixture of a ring and linear isomers. The first has an Eigen core and contributes at high frequencies, whereas the latter accounts for all prominent low-frequency bands. Interestingly, its core is neither a classical Eigen nor a Zundel cation, but rather has hybrid geometry. Such an isomer may play a role in proton conductance along short proton wires.",
author = "Waldemar Kulig and Noam Agmon",
year = "2014",
month = "3",
day = "14",
doi = "10.1039/c3cp54029d",
language = "English",
volume = "16",
pages = "4933--4941",
journal = "Physical Chemistry Chemical Physics",
issn = "1463-9076",
publisher = "Royal Society of Chemistry",
number = "10",

}

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TY - JOUR

T1 - Deciphering the infrared spectrum of the protonated water pentamer and the hybrid Eigen-Zundel cation

AU - Kulig, Waldemar

AU - Agmon, Noam

PY - 2014/3/14

Y1 - 2014/3/14

N2 - Traditionally, infrared band assignment for the protonated water clusters, such as H+(H2O)5, is based on their lowest energy isomer. Recent experiments extend the observation spectral window to lower frequencies, for which such assignment appears to be inadequate. Because this hydrogen-bonded system is highly anharmonic, harmonic spectral calculations are insufficient for reliable interpretation. Consequently, we have calculated the IR spectrum of several isomers of the protonated water pentamer using an inherently anharmonic methodology, utilizing dipole and velocity autocorrelation functions computed from ab initio molecular dynamic trajectories. While the spectrum of H+(H2O)5 is universally assumed to represent the branched Eigen isomer, we find a better agreement for a mixture of a ring and linear isomers. The first has an Eigen core and contributes at high frequencies, whereas the latter accounts for all prominent low-frequency bands. Interestingly, its core is neither a classical Eigen nor a Zundel cation, but rather has hybrid geometry. Such an isomer may play a role in proton conductance along short proton wires.

AB - Traditionally, infrared band assignment for the protonated water clusters, such as H+(H2O)5, is based on their lowest energy isomer. Recent experiments extend the observation spectral window to lower frequencies, for which such assignment appears to be inadequate. Because this hydrogen-bonded system is highly anharmonic, harmonic spectral calculations are insufficient for reliable interpretation. Consequently, we have calculated the IR spectrum of several isomers of the protonated water pentamer using an inherently anharmonic methodology, utilizing dipole and velocity autocorrelation functions computed from ab initio molecular dynamic trajectories. While the spectrum of H+(H2O)5 is universally assumed to represent the branched Eigen isomer, we find a better agreement for a mixture of a ring and linear isomers. The first has an Eigen core and contributes at high frequencies, whereas the latter accounts for all prominent low-frequency bands. Interestingly, its core is neither a classical Eigen nor a Zundel cation, but rather has hybrid geometry. Such an isomer may play a role in proton conductance along short proton wires.

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U2 - 10.1039/c3cp54029d

DO - 10.1039/c3cp54029d

M3 - Article

VL - 16

SP - 4933

EP - 4941

JO - Physical Chemistry Chemical Physics

JF - Physical Chemistry Chemical Physics

SN - 1463-9076

IS - 10

ER -