1967Transactions of the Faraday SocietyRequires access

Nuclear magnetic resonance studies of heterocyclic fluorine compounds. Part 2.—Perfluoro-N-fluoro-piperidine and perfluoro-N-fluoro-morpholine ring systems

J. Lee, Keith G. Orrell

Open publisher page 12 citations

Abstract

The temperature-dependence of the 19F nuclear magnetic resonance spectra of perfluoro-N-fluoro-piperidine and perfluoro-N-fluoro-morpholine has been examined in the range from –74 to 20°C. The changes in appearance of the spectra are interpreted on the basis of the changing rate of chair-to-chair interconversion. There is evidence that, at corresponding temperatures, this interconversion rate is greater for the perfluoro-N-fluoro-morpholine than for the perfluoro-N-fluoro-piperidine ring. The spectra of perfluoro-(N-fluoro-methylpiperidines) are essentially temperature-independent over the range from –90 to 100°C suggesting conformationally rigid structures. The effect of the perfluoromethyl substituent on the vicinal ring fluorines is considered.

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What this paper is about

The temperature-dependence of the 19F nuclear magnetic resonance spectra of perfluoro-N-fluoro-piperidine and perfluoro-N-fluoro-morpholine has been examined in the range from –74 to 20°C. The changes in appearance of the spectra are interpreted on the basis of the changing rate of chair-to-chair interconversion. There is evidence that, at corresponding temperatures, this interconversion rate is greater for the perfluoro-N-fluoro-morpholine than for the perfluoro-N-fluoro-piperidine ring. The spectra of perfluoro-(N-fluoro-methylpiperidines) are essentially temperature-independent over the range from –90 to 100°C suggesting conformationally rigid structures. The effect of the perfluoromethyl substituent on the vicinal ring fluorines is considered.

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Available abstract

The temperature-dependence of the 19F nuclear magnetic resonance spectra of perfluoro-N-fluoro-piperidine and perfluoro-N-fluoro-morpholine has been examined in the range from –74 to 20°C. The changes in appearance of the spectra are interpreted on the basis of the changing rate of chair-to-chair interconversion. There is evidence that, at corresponding temperatures, this interconversion rate is greater for the perfluoro-N-fluoro-morpholine than for the perfluoro-N-fluoro-piperidine ring. The spectra of perfluoro-(N-fluoro-methylpiperidines) are essentially temperature-independent over the range from –90 to 100°C suggesting conformationally rigid structures. The effect of the perfluoromethyl substituent on the vicinal ring fluorines is considered.

Key concepts: Morpholine, Piperidine, Chemistry, Ring (chemistry), Fluorine, Substituent, Vicinal, Spectral line

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Nuclear magnetic resonance studies of heterocyclic fluorine compounds. Part 2.—Perfluoro-N-fluoro-piperidine and perfluoro-N-fluoro-morpholine ring systems — Research Paper | ScholarLens