نمایش مختصر رکورد

dc.contributor.authorHabibi-Khorassani, Sayeyd Mosatfaen_US
dc.contributor.authorMaghsoodlou, Malek Taheren_US
dc.contributor.authorShahraki, Mehdien_US
dc.contributor.authorHashemi Shahri, Marjanen_US
dc.contributor.authorAboonajmi, Jasemen_US
dc.contributor.authorZarei, Tahereen_US
dc.date.accessioned1399-07-09T08:17:43Zfa_IR
dc.date.accessioned2020-09-30T08:17:43Z
dc.date.available1399-07-09T08:17:43Zfa_IR
dc.date.available2020-09-30T08:17:43Z
dc.date.issued2014-12-01en_US
dc.date.issued1393-09-10fa_IR
dc.date.submitted2014-04-09en_US
dc.date.submitted1393-01-20fa_IR
dc.identifier.citationHabibi-Khorassani, Sayeyd Mosatfa, Maghsoodlou, Malek Taher, Shahraki, Mehdi, Hashemi Shahri, Marjan, Aboonajmi, Jasem, Zarei, Tahere. (2014). Kinetics investigation of the synthesis reaction of 2,3-dihydroquinazolin-4(1H)-ones in the presence of acetic acid as a catalyst. Iranian Journal of Catalysis, 4(4), 241-246.en_US
dc.identifier.issn2252-0236
dc.identifier.issn2345-4865
dc.identifier.urihttp://ijc.iaush.ac.ir/article_552422.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/338766
dc.description.abstractAcetic acid has been applied as an efficient catalyst and a green solvent for the two–component condensation reaction consisting of benzaldehyde, 2-amino-benzamide. The advantages of this protocol was excellent yield, short reaction time, mild reaction conditions, higher availability, low costs, more environmentally friendly, lack of need for column chromatography and simple work-up procedure. In addition, based on the spectral data, the partial order with respect to each reactant was one. Furthermore, useful information regarding the mechanism of the reaction was obtained from studies of the effect of solvent, concentration and catalyst on the rate of the reaction. The results showed that the first step of the mechanism was a rate-determining step. In the studied temperature range, the second order rate constant (lnk1, lnk1/T) depended on reciprocal temperature was in good agreement with the Arrhenius and Eyring equations. These data provided the suitable plots for calculating the activation energy (Ea = 52.80 kJmol-1) and the related kinetic parameters (ΔG‡ = 63.74 kJmol-1, ΔS‡ = -54.22 Jmol-1 and ΔH‡ = 50.28 kJmol-1) of the reaction.en_US
dc.format.extent390
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherIslamic Azad University, Shahreza Branchen_US
dc.relation.ispartofIranian Journal of Catalysisen_US
dc.subjectCatalysten_US
dc.subjectKineticsen_US
dc.subjectMechanismen_US
dc.subjectGreen solventen_US
dc.titleKinetics investigation of the synthesis reaction of 2,3-dihydroquinazolin-4(1H)-ones in the presence of acetic acid as a catalysten_US
dc.typeTexten_US
dc.typeArticlesen_US
dc.contributor.departmentDepartment of Chemistry Faculty of Science University of Sistan and Baluchestan Zahedan, Iran P.O. Box: 98135-674en_US
dc.contributor.departmentDepartment of Chemistry Faculty of Science University of Sistan and Baluchestan Zahedan, Iran P.O. Box: 98135-674en_US
dc.contributor.departmentDepartment of Chemistry Faculty of Science University of Sistan and Baluchestan Zahedan, Iran P.O. Box: 98135-674en_US
dc.contributor.departmentDepartment of Chemistry Faculty of Science University of Sistan and Baluchestan Zahedan, Iran P.O. Box: 98135-674en_US
dc.contributor.departmentDepartment of Chemistry Faculty of Science University of Sistan and Baluchestan Zahedan, Iran P.O. Box: 98135-674en_US
dc.contributor.departmentDepartment of Chemistry Faculty of Science University of Sistan and Baluchestan Zahedan, Iran P.O. Box: 98135-674en_US
dc.citation.volume4
dc.citation.issue4
dc.citation.spage241
dc.citation.epage246


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