Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21104
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dc.contributor.authorGupta, Akhilesh K-
dc.contributor.authorPoddar, Raj K-
dc.date.accessioned2013-09-13T09:54:21Z-
dc.date.available2013-09-13T09:54:21Z-
dc.date.issued2000-04-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21104-
dc.description457-460en_US
dc.description.abstract[Ru(acac)3] has been prepared by a new method in high yield and found to be a precursor for the synthesis of [Ru(acac)2L2] (L = a neutral monodentate ligand viz., CH3CN, py, 3Me-py, 4Me-py, dmpzH (3,5-dimethyl pyrazole), PPh3 or AsPh3; L2 = a neutral bidentate ligand, viz, bipy(2,2-bipyridine) or phen (1,10-phenanthroline). All the complexes are new except [Ru(acac)2(CH3CN)2] and [Ru(acac)2(PPh3)2], and are characterized by physical and electrochemical 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.39A(04) [April 2000]en_US
dc.titleImproved synthesis and reactivity of tris( acetylacetonato)ruthenium(III)en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.39A(04) [April 2000]

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