Oligomeric hydroxy-aryloxy phosphazene based on cyclic chlorophosphazenes

Oligomeric hydroxy-aryloxy phosphazene based on cyclic chlorophosphazenes Reaction of hexachlorocyclotriphosphazene and a mixture of cyclic chlorophosphazene [NPCl2] n = 3–8 with an excess of diphenylolpropane under different conditions affords corresponding oligomeric hydroxy-aryloxy phosphazenes, which were characterized by gas chromatography-mass spectrometry, laser mass spectrometry, 31P and 1H NMR spectroscopy. Side reactions was found with participation of decomposition products of diphenylolpropane. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Russian Journal of Applied Chemistry Springer Journals

Oligomeric hydroxy-aryloxy phosphazene based on cyclic chlorophosphazenes

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Publisher
Pleiades Publishing
Copyright
Copyright © 2013 by Pleiades Publishing, Ltd.
Subject
Chemistry; Chemistry/Food Science, general; Industrial Chemistry/Chemical Engineering
ISSN
1070-4272
eISSN
1608-3296
D.O.I.
10.1134/S1070427213120161
Publisher site
See Article on Publisher Site

Abstract

Reaction of hexachlorocyclotriphosphazene and a mixture of cyclic chlorophosphazene [NPCl2] n = 3–8 with an excess of diphenylolpropane under different conditions affords corresponding oligomeric hydroxy-aryloxy phosphazenes, which were characterized by gas chromatography-mass spectrometry, laser mass spectrometry, 31P and 1H NMR spectroscopy. Side reactions was found with participation of decomposition products of diphenylolpropane.

Journal

Russian Journal of Applied ChemistrySpringer Journals

Published: Feb 27, 2014

References

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