Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.11889/7651
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dc.contributor.authorAbuhijleh, A. Latif-
dc.date.accessioned2023-02-09T07:48:50Z-
dc.date.available2023-02-09T07:48:50Z-
dc.date.issued2011-
dc.identifier.urihttp://hdl.handle.net/20.500.11889/7651-
dc.description.abstractMononuclear complex bis(aspirinato) bis(2-methylimidazole) copper(II), Cu(asp)2 (2-MeIm)2 (1), has been synthesized and spectroscopically characterized. The biomimetic catalytic activities of this complex and our previously characterized complexes, Cu(asp)2 (1,2-MeIm)2 (2), Cu(Hsal)2 (1,2-MeIm)2 (3), and Cu(sal)(2- MeIm)3, (4) [H2sal= salicylic acid and MeIm=methylimidazole], for the oxidation of 3,5-di-tert butylcatechol to the corresponding o-quinone and the oxidative dealkylation of 2,4,6-tri-tert-butylphenol to 2,6-di-tert-butyl-1,4-benzoquinone and 4,6-di-tert-butyl-1,2-benzoquinone as the main products are reported. Complexes 1 and 2 are found to be potent SOD mimics and their SOD activities are compared with those obtained previously for complexes 3 and 4.en_US
dc.language.isoenen_US
dc.publisherInorganic Chemistry Communicationsen_US
dc.subjectMononuclear copper(II) aspirinate Catecholase Oxidative dealkylation of phenolen_US
dc.subjectMononuclear copper(II) aspirinateen_US
dc.subjectCatecholaseen_US
dc.subjectSOD mimicsen_US
dc.titleMononuclear copper(ll) aspirinate or salicylate complexes with methylimidazoles as biomimetic catalysts for oxidative dealkylation of a hindered phenol, oxidation of catechol and their superoxide scavenging activitiesen_US
dc.typeArticleen_US
newfileds.departmentScienceen_US
newfileds.item-access-typeopen_accessen_US
newfileds.thesis-prognoneen_US
newfileds.general-subjectnoneen_US
dc.identifier.doi10.1016/j.inoche.2011.02.029-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.languageiso639-1other-
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