Infrared studies of conformational isomerism in some gem-chloronitrosoalkanes

K. M. Evans, S. J. Ireson, M. R S McCoustra, J. Pfab

Research output: Contribution to journalArticle

Abstract

The IR spectra of 2-chloro-2-nitrosopropane, 2-chloro-2-nitrosobutane and 2-chloro-3-methyl-2-nitrosobutane have been studied in the gas phase and solid phase, and in solutions of varying polarity. The spectra reveal clear evidence for the hindered internal rotation of the NO functional group about the CN bond in a splitting of the NO stretching band. The spectra can be interpreted as arising from energetically favoured cis conformational isomers, exhibiting the higher of the observed NO stretching frequencies. In each case, assignment of the lower NO stretching frequency is uncertain on the basis of experimental evidence. The results of semi-empirical molecular orbital calculations, however, support the assignment of this feature to the gauche conformational isomers. Temperature dependent IR spectroscopy has been employed in the determination of conformational enthalpy differences in both the gas phase and non-polar solution, which are then compared to the results of semi-empirical molecular orbital calculations. © 1992.

Original languageEnglish
Pages (from-to)659-669
Number of pages11
JournalSpectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
Volume48
Issue number5
Publication statusPublished - May 1992

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