Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/46650
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dc.contributor.authorSrivastava, A K-
dc.contributor.authorSrivastava, S K-
dc.contributor.authorSingh, Kalpana-
dc.contributor.authorSrivastava, P K-
dc.contributor.authorSingh, V P-
dc.date.accessioned2019-03-26T04:58:11Z-
dc.date.available2019-03-26T04:58:11Z-
dc.date.issued1989-03-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46650-
dc.description237-240en_US
dc.description.abstractArylthiocyanates have been reacted with Co(II) and Ni(II) selenocyanates to get complexes of the general formula (ArSCN)2M(NCSe)2. These complexes further react with pyridine (py), nicotinamide (nia)and morpholine (morph) to form adducts. The complexes have been characterised by various physicochemical data. These complexes have been compared with Blitox 50 W.P., a commercial fungicide, for their antifungal activity against R. Nigricans and A. Niger. In general, cobalt(II) complexes exhibit higher fungicidal activity than nickel (II) complexes.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.28A(03) [March 1989]en_US
dc.titleStructures & Antifungal Activities of Bis-(arylthiocyanato )Metal (II) Selenocyanatesen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(03) [March 1989]

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