Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16615
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dc.contributor.authorSingh, Gurdip-
dc.contributor.authorKapoor, Inder Pal Singh-
dc.contributor.authorSingh, Jyotsna-
dc.date.accessioned2013-03-29T14:51:30Z-
dc.date.available2013-03-29T14:51:30Z-
dc.date.issued1999-09-
dc.identifier.urihttp://hdl.handle.net/123456789/16615-
dc.description1114-1117en_US
dc.description.abstractDi-ortho ring substituted arylammonium sulfates (Di-o-RSAS) have been prepared from the corresponding arylamines by treatment with cone. H2SO4 and characterized by elemental, gravimetric and spectral analyses. These sulfates yield the corresponding ring substituted aminobenzenesulfonic acids (RSABSA) when subjected to thermal energy. Non-isothermal gravimetric studies on di-o-RSAS support the formation of RSABSA. It is observed that most of the salts undergo transformation to acid in solid state via proton transfer reaction prior to sulfonation.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-B Vol.38B(09) [September 1999]en_US
dc.titleSulfonation of arylamines Part 9 - Solid state synthesis of di-ortho ring substituted aminobenzenesulfonic acidsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(09) [September 1999]

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