Dhathathreyan, KS and Krishnamurthy, SS and Murthy, AR Vasudeva and Shaw, Robert A and Woods, Michael (1982) Studies of phosphazenes. Part 14. The tautomerism of oxocyclotriphosphazadienes. In: Dalton Transactions (8). pp. 1549-1554.
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Abstract
The tautomeric behaviour of monohydroxycyclotriphosphazatrienes has been investigated by 31P n.m.r. spectroscopy. These derivatives exist as oxocyclotriphosphazadiene tautomers in which the hydrogen atom is attached to a ring nitrogen atom to the phosphoryl group. Three types of prototropic behaviour are observed : (a) no exchange is detected and only one tautomer is present [e.g. N3HP3(NHBut)2R3O (R = OMe or OEt)]; (b) exchange takes place between two equivalent sites and only one tautomer is observed [e.g. N3HP3R5O (R = OMe or OPh); N3HP3Ph4RO (R = OMe or OEt)]; and (c) exchange occurs between two non-equivalent sites and two tautomers are present [e.g. N3HP3Ph2R3O (R = OMe, OEt, or OPrn)]. It is shown that basicity calculations using substituent constants have predictive value since they are in good agreement with the spectroscopic observations.
Item Type: | Journal Article |
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Publication: | Dalton Transactions |
Publisher: | Royal Society of Chemistry |
Additional Information: | Copyright of this article belongs to Royal Society of Chemistry. |
Department/Centre: | Division of Chemical Sciences > Inorganic & Physical Chemistry |
Date Deposited: | 29 Dec 2009 11:53 |
Last Modified: | 19 Sep 2010 05:36 |
URI: | http://eprints.iisc.ac.in/id/eprint/21253 |
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