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dc.creatorBohn, Robert K.en_US
dc.creatorWiberg, K. B.en_US
dc.creatorMunrow, Michaeleen R.en_US
dc.date.accessioned2006-06-15T19:14:37Z
dc.date.available2006-06-15T19:14:37Z
dc.date.issued1999en_US
dc.identifier1999-MH-03en_US
dc.identifier.urihttp://hdl.handle.net/1811/19267
dc.description$^{a}$ G. I. L. Jones. D.G. Lister, N.L. Owen, M.C.L. Gerry, and P. Palmieri, J. Molcc. Spectrosc. 60, 348 (1976).en_US
dc.descriptionAuthor Institution: Dept. of Chemistry, University of Connecticut; Dept. of Chemistry, Yale University; Dept. of Chemistry, Wesleyan Universityen_US
dc.description.abstractThe pulsed-jet, Fourier Transform microwave spectrum of methyl thiolformate $(HCOSCH_{3})$ has been observed in the 5-20 GHz region. An earlier $study^{a}$ observed no internal rotation doublets. Those authors noted that either the internal rotation splitting was too small to be observed or much larger than exists in methyl formate. They chose the former interpretation, an unlucky choice, which implies a methyl barrier greater than $2.5 kcal/mol$. The compound exists in a conformation with the methyl group eclipsing the carbonyl oxygen. Spectra of the parent isotopomer and the $^{33}S$ (with assigned quadrupole splittings), $^{34}S$, and both $^{13}C$ isotopomers have been assigned including both A- and E-state transitions arising from methyl internal rotation. The 3-fold barrier is $147-8 cm^{-1}$ (420 cal/mol) in the various isotopomers.en_US
dc.format.extent105469 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleMETHYL INTERNAL ROTATION IN METHYL THIOLFORMATE $(HCOSCH_{3})$en_US
dc.typearticleen_US


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