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Structure and bonding in cyclic phosphoramidates as determined by carbon-13 magnetic resonance
- Source :
- Canadian Journal of Chemistry. 57:21-26
- Publication Year :
- 1979
- Publisher :
- Canadian Science Publishing, 1979.
-
Abstract
- 13C chemical shifts and 13C–31P couplings are reported for 11 cyclic phosphoramidates of ring sizes from four to nine. Vicinal couplings are compared with those of carbocyclic analogs and provide insight regarding the degree of nitrogen lone pair derealization into the N—P bond. For six-membered and larger rings, there appears to be nearly complete lone pair delocalization, i.e., a trigonal planar nitrogen atom. In azetidine derivatives the nitrogen lone pair remains localized, giving rise to a highly puckered ring conformation. Pyrrolidine derivatives are viewed as having a nitrogen with a partially delocalized electron pair.
Details
- ISSN :
- 14803291 and 00084042
- Volume :
- 57
- Database :
- OpenAIRE
- Journal :
- Canadian Journal of Chemistry
- Accession number :
- edsair.doi...........4d2caaa9953588ec682f5327212b14d6