Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/18628
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dc.contributor.authorGoyal, Sunita-
dc.contributor.authorSingh, Anirudh-
dc.date.accessioned2013-06-03T05:24:45Z-
dc.date.available2013-06-03T05:24:45Z-
dc.date.issued2001-12-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/18628-
dc.description1302-1306en_US
dc.description.abstractReactions in 1:1 molar ratio of OGOSb(OPr1) (where G = CHMeCH2CMe2 and CMe2CH2CH2CMe2) with N-arylsalicylaldimines (LH = HOC6H4CH=NAr (where Ar = Ph, 2,6-R2C6H3 (R = Me, Et, Pr1), 2,4,6-Me3C6H2)) in benzene afford new cyclic compounds of antimony containing salicylaldiminate and 2-methylpentane-2,4-diolate and 2,5-dimethylhexane-2,5-diolate groups. Characterization of all these derivatives have been carried out by elemental analysis, molecular weight determinations, IR and 1H NMR spectroscopic studies.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.40A(12) [December 2001]en_US
dc.titlePreparation and characterization of mixed glycolate-salicylaldiminate derivatives of antimony(III)en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.40A(12) [December 2001]

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