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Application of 13C NMR spectroscopy in the assignment of 1H NMR signals of nonequivalent SCH3 groups.

dc.contributor.advisorNova Scotian Institute of Science
dc.contributor.authorHooper, Donald L.
dc.contributor.authorGrossert, J.Stuart
dc.contributor.authorNeaves, W. M. (William Maynard), 1954-
dc.date.accessioned2012-08-10T19:03:30Z
dc.date.available2012-08-10T19:03:30Z
dc.date.issued1985-09
dc.description.abstractThe SCH3 groups of 3- and/or 5 alkyl substituted 2,4,6-trithiaheptanes have almost identical chemical shifts in both 1H and 13C nmr spectra. A combination of gated decoupling and single frequency off-resonance decoupling, followed by the construction of graphs of the type proposed by Pachler, allows the assignment of the 1H nmr signals.en_US
dc.identifier.citationHooper, D.L., Grossert, J.S., Neaves, W.M. (1985). Application of 13C NMR spectroscopy in the assignment of 1H NMR signals of nonequivalent SCH3 groups. Proceedings and Transactions of the Nova Scotian Institute of Science, 35(1), 17-25.en_US
dc.identifier.urihttp://hdl.handle.net/10222/15212
dc.language.isoenen_US
dc.publisherDalhousie Printing Centreen_US
dc.subjectSpectrum analysisen_US
dc.subjectChemistryen_US
dc.titleApplication of 13C NMR spectroscopy in the assignment of 1H NMR signals of nonequivalent SCH3 groups.en_US
dc.typeTexten_US

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