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

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dc.authorscopusid6701793097
dc.authorscopusid46462159400
dc.contributor.authorKütük, H.
dc.contributor.authorYakan, H.
dc.date.accessioned2020-06-21T14:46:28Z
dc.date.available2020-06-21T14:46:28Z
dc.date.issued2011
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Kütük] Halil, Department of Chemistry, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yakan] Hasan, Department of Chemistry, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_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° 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. © 2011 Taylor & Francis Group, LLC.en_US
dc.identifier.doi10.1080/10426507.2010.517584
dc.identifier.endpage1469en_US
dc.identifier.issn1042-6507
dc.identifier.issn1563-5325
dc.identifier.issue7en_US
dc.identifier.scopus2-s2.0-80051494464
dc.identifier.scopusqualityQ4
dc.identifier.startpage1460en_US
dc.identifier.urihttps://doi.org/10.1080/10426507.2010.517584
dc.identifier.volume186en_US
dc.identifier.wosWOS:000299725800009
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.ispartofPhosphorus Sulfur and Silicon and the Related Elementsen_US
dc.relation.journalPhosphorus Sulfur and Silicon and the Related Elementsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_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 Arylthio) Phthalimidesen_US
dc.typeArticleen_US
dspace.entity.typePublication

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