The ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolution

The laser excitation spectrum of the 327 nm band system of CoCl2, formed in a free-jet expansion, has been recorded at a rotational temperature of approximately 10 K. The spectrum is congested and suffers extensive perturbations. A progression in the excited state symmetric stretching vibration has...

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Main Authors: Hodges, P, Brown, J, Varberg, T
Format: Journal article
Language:English
Published: American Institute of Physics 2006
Subjects:
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author Hodges, P
Brown, J
Varberg, T
author_facet Hodges, P
Brown, J
Varberg, T
author_sort Hodges, P
collection OXFORD
description The laser excitation spectrum of the 327 nm band system of CoCl2, formed in a free-jet expansion, has been recorded at a rotational temperature of approximately 10 K. The spectrum is congested and suffers extensive perturbations. A progression in the excited state symmetric stretching vibration has been identified. The decrease in the symmetric stretching vibrational wave number on excitation is considerable [v'1=195.7(12), v''1=358.1(17) cmˉ¹]. Despite widespread perturbations in the rotational structure of these vibronic bands, they can be confidently assigned to a parallel Ω=7/2-7/2 transition, consistent with an inverted 4Δg ground electronic state. The rotational constant for Co35Cl2 in the ground state is determined to be 0.056 65(11) cmˉ¹, which corresponds to a value for the zero-point averaged Co-Cl bond length ro of 2.062 8(40)Å. The perturbations are found to be strongly isotopomer dependent.
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spelling oxford-uuid:c5706092-0327-4362-ab0a-9814aeac0ebc2022-03-27T06:30:55ZThe ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolutionJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c5706092-0327-4362-ab0a-9814aeac0ebcPhysical & theoretical chemistryChemistry & allied sciencesEnglishOxford University Research Archive - ValetAmerican Institute of Physics2006Hodges, PBrown, JVarberg, TThe laser excitation spectrum of the 327 nm band system of CoCl2, formed in a free-jet expansion, has been recorded at a rotational temperature of approximately 10 K. The spectrum is congested and suffers extensive perturbations. A progression in the excited state symmetric stretching vibration has been identified. The decrease in the symmetric stretching vibrational wave number on excitation is considerable [v'1=195.7(12), v''1=358.1(17) cmˉ¹]. Despite widespread perturbations in the rotational structure of these vibronic bands, they can be confidently assigned to a parallel Ω=7/2-7/2 transition, consistent with an inverted 4Δg ground electronic state. The rotational constant for Co35Cl2 in the ground state is determined to be 0.056 65(11) cmˉ¹, which corresponds to a value for the zero-point averaged Co-Cl bond length ro of 2.062 8(40)Å. The perturbations are found to be strongly isotopomer dependent.
spellingShingle Physical & theoretical chemistry
Chemistry & allied sciences
Hodges, P
Brown, J
Varberg, T
The ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolution
title The ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolution
title_full The ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolution
title_fullStr The ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolution
title_full_unstemmed The ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolution
title_short The ultraviolet spectrum of the CoCl2 radical, studied at vibrational and rotational resolution
title_sort ultraviolet spectrum of the cocl2 radical studied at vibrational and rotational resolution
topic Physical & theoretical chemistry
Chemistry & allied sciences
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