Electron spin resonance study of phosphorus-nitroxides from 1,3-additions of silicon-phosphorus reagents to nitrones.

Autor: Haire DL; Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, N1G 2W1, Canada. lhaire@uoguelph.ca, Janzen EG, Robinson VJ, Hrvoic I
Jazyk: angličtina
Zdroj: Magnetic resonance in chemistry : MRC [Magn Reson Chem] 2004 Oct; Vol. 42 (10), pp. 835-43.
DOI: 10.1002/mrc.1436
Abstrakt: This article explores a new, convenient route to beta-phosphorus nitroxides. Specifically, the reaction sequence involves the novel 1,3-addition of trimethylsilyl phosphites (e.g. diethyl) or trimethylsilyl phosphines (e.g. diphenyl) to aldo-nitrones [e.g. alpha-phenyl-N-tert-butylnitrone (PBN) or 5,5-dimethyl-l-pyrroline-N-oxide (DMPO)] or keto-nitrones [e.g. 2-ethyl-5,5-dimethyl-1 pyrroline-N-oxide (2-Et-DMPO) or 2-phenyl-5,5-dimethyl-l-pyrroline-N-oxide (2-Ph-DMPO)] to form alpha-phosphityl- or alpha-phosphinyl-O-silylhydroxylamines. Acidic hydrolysis provides the corresponding hydroxylamines that are easily oxidized to the title beta-phosphorus-nitroxides. ESR spectroscopic analysis revealed some very large beta-phosphorus hyperfine splittings (i.e. in excess of 5 mT). For this reason and their remarkable stability (persistence) some of these nitroxides show promise as integral components in new, improved weak-field dynamic nuclear polarization (DNP) magnetometers.
(Copyright 2004 John Wiley & Sons, Ltd.)
Databáze: MEDLINE
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