Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/18267
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dc.contributor.authorSugunan, S-
dc.contributor.authorNishamol, K-
dc.date.accessioned2013-05-20T10:36:03Z-
dc.date.available2013-05-20T10:36:03Z-
dc.date.issued2002-05-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/18267-
dc.description928-933en_US
dc.description.abstractThe liquid-phase Friedel-Crafts acylation of toluene using benzoyl chloride as benzoylating agent has been carried out over NixMn(1-x)Fe2O4 (x=0, 0.2, 0.4, 0. 6, 0.8 and 1.0) type systems under different reaction conditions. It is observed that the systems with high 'x' values are effective for the conversion of BOC and the selective formation of 4-MBP. Selectivity for 4-MBP over Mn Fe2O4 is more than 90% under the optimized reaction conditions. Sites of moderate acidity is effective in catalyzing the benzoylation reaction.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.41A(05) [May 2002]en_US
dc.titleLiquid-phase Friedel-Crafts acylation using NixMn(1-x)Fe2O4 spinel catalystsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.41A(05) [May 2002]

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