Mechanism of nucleophilic substitution reactions of 4-(4ˊ-nitro)phenylnitrobenzofurazan ether with aniline in acetonitrile

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dc.contributor.authorGbayo, K.
dc.contributor.authorIsanbor, C.
dc.contributor.authorLobb, K.
dc.contributor.authorOloba-Whenu, O.
dc.date.accessioned2019-08-26T17:17:15Z
dc.date.available2019-08-26T17:17:15Z
dc.date.issued2017-08-02
dc.description.abstractRate constants and activation parameters obtained for the nucleophilic aromatic substitution reactions (SNAr) of 4-substitutedphenoxy-7-nitrobenzoxadiazole (1) with aniline in acetonitrile at varying temperature using Nuclear Magnetic Resonance (NMR) techniques were reported. These results were compared with the theoretical study which identifies transformations and intermediates using Density Functional Theory (DFT).en_US
dc.identifier.citationGbayo, K., Isanbor, C., Lobb, K., & Oloba-Whenu, O. (2017). Mechanism of nucleophilic substitution reactions of 4-(4ˊ-nitro) phenylnitrobenzofurazan ether with aniline in acetonitrile. Physical Sciences Reviews, 2(10).en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/4785
dc.language.isoen_USen_US
dc.publisherDe Gruyteren_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistry::Theoretical chemistry::Quantum chemistryen_US
dc.subjectNucleophilic aromatic substitutionen_US
dc.subjectDFTen_US
dc.subjectNMRen_US
dc.titleMechanism of nucleophilic substitution reactions of 4-(4ˊ-nitro)phenylnitrobenzofurazan ether with aniline in acetonitrileen_US
dc.typeArticleen_US
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