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The Mechanisms of Acid-Catalyzed Hydrolysis of N-(4-Substituted Arylthio) Phthalimides

dc.contributor.authorKutuk, Halil
dc.contributor.authorYakan, Hasan
dc.date.accessioned2020-06-21T14:46:28Z
dc.date.available2020-06-21T14:46:28Z
dc.date.issued2011
dc.identifier.issn1042-6507
dc.identifier.urihttps://doi.org/10.1080/10426507.2010.517584
dc.identifier.urihttps://hdl.handle.net/20.500.12712/17562
dc.descriptionWOS: 000299725800009en_US
dc.description.abstractThe acid-catalyzed hydrolysis of N-(4-substitutedarylthio)phthalimides was studied in aqueous solutions of sulfuric, perchloric, and hydrochloric acids at 40.0 +/- 0.1 degrees C. Analysis of the data by the excess acidity method, activation parameters, and substituent effects indicates hydrolysis by an A-2 mechanism at low acidity. At higher acidities, a changeover to an A-1 mechanism is observed.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.isversionof10.1080/10426507.2010.517584en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcid-catalyzed hydrolysisen_US
dc.subjectarylthiophthalimidesen_US
dc.subjectexcess acidityen_US
dc.subjectsulfenimidesen_US
dc.titleThe Mechanisms of Acid-Catalyzed Hydrolysis of N-(4-Substituted Arylthio) Phthalimidesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume186en_US
dc.identifier.issue7en_US
dc.identifier.startpage1460en_US
dc.identifier.endpage1469en_US
dc.relation.journalPhosphorus Sulfur and Silicon and the Related Elementsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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