Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/46560
Title: Synthesis and reactions of alkoxyzirconium(IV) O,O-alkylen dithiophosphates
Authors: Yadav, J S
Mehrotra, R K
Srivastava, G
Issue Date: Dec-1990
Publisher: NISCAIR-CSIR, India
Abstract: Reactions of Zr(OPri)4·PriOH with O,O-alkylene dithiophosphoric acids in equimolar ratio yield trisopropoxyzirconium alkylene dithiophosphates, (PriO)3 ZrS(S) (G = - C(Me)2C(Me)2-, -CH(Me) CH(Me)-, -CH2C(Me)2CH2- and -CH2C(Et)2C2-) as hydrolysable, white microcrystalline solids, sol ble in common organic solvents and dimeric in nature. Further replacement of isopropoxy group by dithiophosphato moieties is extremely slow but can be carried out up to the formation of (PriO)2Zr[S(S)]2 which is monomeric in benzene. The IR and NMR (1H, 13C, 31P) data of all the compounds are consistent with the presence of chelating dithiophosphate groups and octahedral structures, the dimerisation in the triisopropoxy derivatives occurring through isopropoxy ridges. Alcoholysis reactions of isopropoxy derivatives with butanol have also been studied.
Page(s): 1212-1214
URI: http://nopr.niscair.res.in/handle/123456789/46560
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.29A(12) [December 1990]

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