Optical spectroscopy of tungsten carbide (WC)

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Publication Type Journal Article
School or College College of Science
Department Chemistry
Creator Morse, Michael David
Other Author Sickafoose, Shane M.; Smith, Adam W.
Title Optical spectroscopy of tungsten carbide (WC)
Date 2002
Description Resonant two-photon ionization spectroscopy has been used to study the diatomic transition-metal carbide, WC. A low-resolution scan revealed a five-member vibrational progression beginning with the 0-0 band at 17 585 cm-1. Analysis of this progression yielded a vibrational frequency of ?'e8(184W12C)=752.6(4.9) cm-1 and a bond length of r'e8(184W12C)=1.747(4) ?. Several unassigned bands were also rotationally resolved and analyzed. All of the observed bands are ?'=2??"=1 transitions, confirming the predicted ground state of 3?1 arising from a 14??8rr?15??4?116?1 configuration. The measured line positions in these bands were simultaneously fitted to provide B"=0.509 66(10) cm-1 for 184W12C, corresponding to r"0(184W12C)=1.713 5(2) ?. These values are corrected for spin-uncoupling effects in the ground state and represent our best estimate of the true bond length of WC. Dispersed fluorescence studies provide the ground-state vibrational constants of ?e=983(4) cm-1 and ?exe=11(1) cm-1, and have also permitted the low-lying [1.2] 3?2 and [4.75] states to be located and characterized. These results on WC are discussed in relation to the isovalent molecule MoC and other transition-metal carbides.
Type Text
Publisher American Institute of Physics (AIP)
Volume 116
Issue 3
First Page 993
Last Page 1002
DOI 10.1063/1.1427068
Language eng
Bibliographic Citation Sickafoose, S. M., Smith, A. W., & Morse, M. D. (2002). Optical spectroscopy of tungsten carbide (WC). Journal of Chemical Physics, 116(3). 993-1002.
Rights Management ©American Institute of Physics. The following article appeared in Sickafoose, S. M., Smith, A. W., & Morse, M. D. (2002). Optical spectroscopy of tungsten carbide (WC). Journal of Chemical Physics, 116(3). 993-1002. and may be found at DOI: 10.1063/1.1427068.
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Reference URL https://collections.lib.utah.edu/ark:/87278/s6ng57x4
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