Millimeter-Wave and High-Resolution Infrared Spectroscopy of the Ground and Seven Lowest Fundamental States of 1<i>H</i>-1,2,4-Triazole

A combined analysis of millimeter-wave (70-700 GHz) and rotationally resolved infrared (400-1200 cm<sup>-1</sup>) spectra of the ground state and seven fundamental vibrational modes of 1<i>H</i>-1,2,4-triazole is reported. While the lowest-energy vibrationally excited state (ν<sub>18</sub>) is well-treated using a single-state distorted-rotor Hamiltonian, the second (ν<sub>17</sub>) and third (ν<sub>16</sub>) vibrationally excited states are involved in strong <i>c</i>-type Coriolis coupling and require an appropriate two-state Hamiltonian. The oblate nature of 1<i>H</i>-1,2,4-triazole is sufficiently close to the oblate symmetric-top limit that the analysis requires the use of A-reduced, sextic centrifugally distorted-rotor Hamiltonian models in the I<sup><i>r</i></sup> representation in order to achieve low σ<sub>fit</sub> values. The coupling between ν<sub>17</sub> (A″) and ν<sub>16</sub> (A″) resulted in many transitions with slightly perturbed frequencies, many highly displaced resonant intrastate transitions, and 165 nominal interstate transitions. Modeling the spectra of ν<sub>17</sub> and ν<sub>16</sub> required three <i>c</i>-axis Coriolis-coupling terms (<i>F</i><sub><i>ab</i></sub>, <i>F</i><sub><i>ab</i></sub><sup><i>J</i></sup>, and <i>F</i><sub><i>ab</i></sub><sup><i>K</i></sup>) to treat the interaction. Many of the nominal interstate transitions form clearly discernible Q-branch bands, comprising degenerate sets of <i>a</i>- and <i>b</i>-type transitions. The rotational spectra of four higher-energy vibrationally excited states (ν<sub>15</sub>, ν<sub>14</sub>, ν<sub>13</sub>, and ν<sub>12</sub>), which form a complex polyad involving Coriolis and anharmonic coupling interactions, were analyzed by single-state models, thus producing only effective spectroscopic constants. Inclusion of rotationally resolved infrared transitions enabled the accurate and precise determination of vibrational band origins for the four lowest-energy fundamental states: ν<sub>18</sub> = 542.601 824 3 (28) cm<sup>-1</sup>, ν<sub>17</sub> = 665.183 128 5 (43) cm<sup>-1</sup>, ν<sub>16</sub> = 682.256 910 5 (43) cm<sup>-1</sup>, and ν<sub>15</sub> = 847.557 400 (11) cm<sup>-1</sup>.

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Publication Details

Journal
The Journal of Physical Chemistry A
Published
2024-08-09
DOI
https://doi.org/10.1021/acs.jpca.4c03890
Citations
3
Primary Topic
Molecular Spectroscopy and Structure
Type
article
Field-Weighted Citation Impact
0.72

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article

Millimeter-Wave and High-Resolution Infrared Spectroscopy of the Ground and Seven Lowest Fundamental States of 1H-1,2,4-Triazole

Robert J. McMahon, Hayley Bunn, Brian J. Esselman, Maria A. Zdanovskaia et al.
3 citations
The Journal of Physical Chemistry A
Molecular Spectroscopy and Structure
0.72
article

Millimeter-Wave and High-Resolution Infrared Spectroscopy of the Ground and Seven Lowest Fundamental States of 1H-1,2,4-Triazole

Robert J. McMahon, Hayley Bunn, Brian J. Esselman, Maria A. Zdanovskaia, Brant Billinghurst, R. Claude Woods, Susanna L. Widicus Weaver, Jianbao Zhao
article en
3 citations

Abstract

A combined analysis of millimeter-wave (70-700 GHz) and rotationally resolved infrared (400-1200 cm<sup>-1</sup>) spectra of the ground state and seven fundamental vibrational modes of 1<i>H</i>-1,2,4-triazole is reported. While the lowest-energy vibrationally excited state (ν<sub>18</sub>) is well-treated using a single-state distorted-rotor Hamiltonian, the second (ν<sub>17</sub>) and third (ν<sub>16</sub>) vibrationally excited states are involved in strong <i>c</i>-type Coriolis coupling and require an appropriate two-state Hamiltonian. The oblate nature of 1<i>H</i>-1,2,4-triazole is sufficiently close to the oblate symmetric-top limit that the analysis requires the use of A-reduced, sextic centrifugally distorted-rotor Hamiltonian models in the I<sup><i>r</i></sup> representation in order to achieve low σ<sub>fit</sub> values. The coupling between ν<sub>17</sub> (A″) and ν<sub>16</sub> (A″) resulted in many transitions with slightly perturbed frequencies, many highly displaced resonant intrastate transitions, and 165 nominal interstate transitions. Modeling the spectra of ν<sub>17</sub> and ν<sub>16</sub> required three <i>c</i>-axis Coriolis-coupling terms (<i>F</i><sub><i>ab</i></sub>, <i>F</i><sub><i>ab</i></sub><sup><i>J</i></sup>, and <i>F</i><sub><i>ab</i></sub><sup><i>K</i></sup>) to treat the interaction. Many of the nominal interstate transitions form clearly discernible Q-branch bands, comprising degenerate sets of <i>a</i>- and <i>b</i>-type transitions. The rotational spectra of four higher-energy vibrationally excited states (ν<sub>15</sub>, ν<sub>14</sub>, ν<sub>13</sub>, and ν<sub>12</sub>), which form a complex polyad involving Coriolis and anharmonic coupling interactions, were analyzed by single-state models, thus producing only effective spectroscopic constants. Inclusion of rotationally resolved infrared transitions enabled the accurate and precise determination of vibrational band origins for the four lowest-energy fundamental states: ν<sub>18</sub> = 542.601 824 3 (28) cm<sup>-1</sup>, ν<sub>17</sub> = 665.183 128 5 (43) cm<sup>-1</sup>, ν<sub>16</sub> = 682.256 910 5 (43) cm<sup>-1</sup>, and ν<sub>15</sub> = 847.557 400 (11) cm<sup>-1</sup>.

The Journal of Physical Chemistry AVol. 128(33)
University of Wisconsin–Madison (US), University of Saskatchewan (CA), Canadian Light Source (Canada) (CA)
University of Wisconsin-Madison, Division of Chemical, Bioengineering, Environmental, and Transport Systems
Openalex Percentile: Top 34%
Molecular Spectroscopy and Structure
0.72
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