Resonant two-photon ionization spectroscopy of jet-cooled PtSi

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Publication Type Journal Article
School or College College of Science
Department Chemistry
Creator Morse, Michael David
Other Author Shao, Lian; Sickafoose, Shane M.; Langenberg, Jon D.; Brugh, Dale J.
Title Resonant two-photon ionization spectroscopy of jet-cooled PtSi
Date 1999
Description Jet-cooled diatomic PtSi, produced in a laser ablation supersonic expansion source, has been spectroscopically investigated between 17 400 and 24 000 cm-1 by resonant two-photon ionization spectroscopy. Two vibrational progressions are observed and identified as the [15.7]?'=1 ?X 1?+ and [18.5]?'=1 ?X 1?+ band systems. Three bands in the former system and six bands in the latter system were rotationally resolved and analyzed, leading to bond lengths of r'e=2.1905(13) ? and r'e=2.2354(3) ? for the [15.7]?'=1 and [18.5]?'=1 states, respectively. The ?"=0 ground state of PtSi is assigned as a 1?+ state, in agreement with previous work and with the assigned ground states of the isovalent NiC, PdC, PtC, and NiSi molecules. The ground state bond length of PtSi is given by r'o=2.0629(2) ?. A Rydberg?Klein?Rees analysis of the ground and excited state potential energy curves is presented, along with a discussion of the chemical bonding and a comparison to the isoelectronic molecule, AlAu. Evidence is presented for a double bond in PtSi, as opposed to a single bond in AlAu.
Type Text
Publisher American Institute of Physics (AIP)
Volume 112
Issue 9
First Page 4118
Last Page 4123
DOI 10.1063/1.480960
Language eng
Bibliographic Citation Shao, L., Sickafoose, S. M., Langenberg, J. D., Brugh, D. J., & Morse, M. D. (1999). Resonant two-photon ionization spectroscopy of jet-cooled PtSi. Journal of Chemical Physics, 112(9), 4118-23.
Rights Management ©American Institute of Physics. The following article appeared in Shao, L., Sickafoose, S. M., Langenberg, J. D., Brugh, D. J., & Morse, M. D. (1999). Resonant two-photon ionization spectroscopy of jet-cooled PtSi. Journal of Chemical Physics, 112(9), 4118-23. and may be found at doi:10.1063/1.480960.
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Reference URL https://collections.lib.utah.edu/ark:/87278/s6dz0sw2
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