(31)P solid state NMR study of structure and chemical stability of dichlorotriphenylphosphorane

2009 John Wiley & Sons, Ltd.

Détails bibliographiques
Publié dans:Magnetic resonance in chemistry : MRC. - 1985. - 47(2009), 6 vom: 15. Juni, Seite 461-4
Auteur principal: Gonnella, Nina C (Auteur)
Autres auteurs: Busacca, Carl, Campbell, Scot, Eriksson, Magnus, Grinberg, Nelu, Bartholomeyzik, Teresa, Ma, Shengli, Norwood, Daniel L
Format: Article en ligne
Langue:English
Publié: 2009
Accès à la collection:Magnetic resonance in chemistry : MRC
Sujets:Journal Article Phosphoranes Phosphorus Isotopes
Description
Résumé:2009 John Wiley & Sons, Ltd.
Solid state (31)P NMR spectroscopy was used to examine, monitor and quantify the compound integrity of the chemical reagent dichlorotriphenylphosphorane. Comparison was also made with solution (31)P NMR spectra which showed that this highly reactive species could be observed in dry benzene prior to conversion to the hydrolyzed product. This is the first reported solid state NMR study of the stability and reactivity of dichlorotriphenylphosphorane and the first account of its observation and comparison in the solution state. In the solid state, the ionic and covalent forms for dichlorotriphenylphosphorane were observed along with hydrolyzed products, however, the degree of hydrolysis was dependent upon the rotor packing conditions. Calculation of the relative percent composition of dichlorotriphenylphosphorane with hydrolyzed product was made for samples prepared in air versus under nitrogen atmosphere. This information was critical in adjusting the amount of reagent used in chemical development syntheses and scale up laboratories. All hydrolyzed products were identified, based upon chemical comparisons with spectra of pure materials
Description:Date Completed 10.07.2009
Date Revised 11.05.2009
published: Print
Citation Status MEDLINE
ISSN:1097-458X
DOI:10.1002/mrc.2412