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Please use this identifier to cite or link to this item: http://10.10.120.238:8080/xmlui/handle/123456789/595
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dc.contributor.authorKulesa K.M.en_US
dc.contributor.authorPadilha D.S.en_US
dc.contributor.authorThapa B.en_US
dc.contributor.authorMazumder S.en_US
dc.contributor.authorLosovyj Y.en_US
dc.contributor.authorSchlegel H.B.en_US
dc.contributor.authorScarpellini M.en_US
dc.contributor.authorVerani C.N.en_US
dc.date.accessioned2023-11-30T08:42:47Z-
dc.date.available2023-11-30T08:42:47Z-
dc.date.issued2023-
dc.identifier.issn0162-0134-
dc.identifier.otherEID(2-s2.0-85148703193)-
dc.identifier.urihttps://dx.doi.org/10.1016/j.jinorgbio.2023.112162-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/595-
dc.description.abstractThe prototypical drug carrier [CoII(L1)Cl]PF6 (1), where L1 is a tripodal amine bound to pyridine and methyl-imidazoles, had its electrocatalytic water splitting activity studied under different pH conditions. This species contains a high-spin 3d7 CoII metal center, and is capable of generating both H2 from water reduction and O2 from water oxidation. Turnover numbers reach 390 after 3 h for water reduction. Initial water oxidation activity is molecular, with TONs of 71 at pH 7 and 103 at pH 11.5. The results reveal that species 1 can undergo several redox transformations, including reduction to the 3d8 CoI species that precedes a LS3d6 hydride for water reduction, as well as nominal CoIV[dbnd]O and CoIII-OOH species required for water oxidation. Post-catalytic analyses confirm the molecular nature of reduction and support initial molecular activity for oxidation. © 2023en_US
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.sourceJournal of Inorganic Biochemistryen_US
dc.subjectBioinorganicen_US
dc.subjectCobalt complexen_US
dc.subjectDrug carrier repurposeden_US
dc.subjectElectrocatalysisen_US
dc.subjectWater oxidationen_US
dc.subjectWater reductionen_US
dc.titleA bioinspired cobalt catalyst based on a tripodal imidazole/pyridine platform capable of water reduction and oxidationen_US
dc.typeJournal Articleen_US
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