
Journal of Organometallic Chemistry p. 301 - 308 (1988)
Update date:2022-08-05
Topics:
Pandey, J. N.
Srivastava, G.
O-Alkyl O'-triorganostannyl phosphonates, R3SnOP(O)(H)OR' (R=Me, Bun, Ph; R'=Me and Et) have been obtained in excellent yield by the reactions of sodium salts of O-alkyl phosphonic acids with triorganotin chlorides.The triphenyltin derivatives are insoluble, high melting, white crystalline solids, whereas the trialkyltin derivatives are colourless, non-volatil, thermally and hydrolytically stable, viscous liquids, miscible with common organic solvents.Their molecular weights are concentration- as well as solvent-dependent.The IR and 1H, 13C, 31P, and 119Sn NMR spectral data are consistent with a polymeric structure involving planar triorganotin groups linked by phosphonate bridges.The two axial Sn-O-P bonds become equivalent as a result of strong P=O->Sn coordination.Some reactions of the triorganostannyl alkyl phosphonates have also been studied.
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