Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/40359
Title: Cyclic sulphur-nitrogen compounds and phosphorus reagents: Part XIII1-Reactions of cyclic sulphur-nitrogen chlorides with Ph3P-influences of tertiary base, Et3N and the ring size of the cyclothiazyl chloride on the product formation
Authors: Mohan, T
Senthivel, P
Rao, M N Sudheendra
Issue Date: Dec-1995
Publisher: NISCAIR-CSIR, India
Abstract: Similar to the reactions with S4N3Cl and S3N3Cl3,triphenylphosphine reacts with five-membered cyclic sulphur-nitrogen chlorides namely, S3N2Cl and S3N2Cl2 to give triphenylphosphiniminium chloride, Ph3P=NHCl- as the major product. Maximum yield (ca. 90%) is obtained when triphenylphosphine is reacted with S3N2Cl in acetonitrile at room temperature in 2:1 molar ratio. Analogous reactions performed in presence of triethylamine afford two cyclothiazene products containing phosphinimino substituent. The ring size of the S-N chloride seems to determine the nature of phosphiniminocyclothiazenes formed. A rationalization of the results obtained has been attempted.
Page(s): 961-966
URI: http://nopr.niscair.res.in/handle/123456789/40359
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.34A(12) [December 1995]

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