Karthikeyan, Sakthivel and Krishnamurthy, Setharampattu S (1991) Studies of phosphazenes. Part 33. Thermal rearrangement of alkoxy(p-methylphenoxy)cyclophosphazenes: a synthetic route to oxocyclophosphazanes, phosphazadienes and phosphaz-1-enes. In: Dalton Transactions (2). pp. 299-306.
ntr.pdf - Published Version
Restricted to Registered users only
Download (795Kb) | Request a copy
The aryloxy(alkoxy)cyclotriphosphazenes N3P3(OR)6ï¿½m(OC6H4Me-p)n(R = Me, n= 1ï¿½3; R = Et or CH2Ph, n= 3) rearrange on heating to give trioxocyclotriphosphazanes; the di- and mono-methoxy derivatives, N3P3(OMe)6ï¿½n(OC6H4Me-p)n(n= 4 or 5), yield dioxophosphaz-1-enes and an oxophosphazadiene respectively. The 1H, 13C and 31P NMR data for the starting materials and the products are presented. No evidence has been found for partially rearranged products. The geometrical disposition of the aryloxy groups in the starting material is retained in the rearranged products. Some aspects of the mechanism of the thermal rearrangement are discussed.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to Royal Society of Chemistry.|
|Department/Centre:||Division of Chemical Sciences > Inorganic & Physical Chemistry|
|Date Deposited:||30 Nov 2010 13:56|
|Last Modified:||01 Dec 2010 06:03|
Actions (login required)