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DC Field | Value | Language |
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dc.citation.endPage | 9943 | - |
dc.citation.number | 14 | - |
dc.citation.startPage | 9938 | - |
dc.citation.title | INORGANIC CHEMISTRY | - |
dc.citation.volume | 59 | - |
dc.contributor.author | Kim, Bohee | - |
dc.contributor.author | Kim, Seonghan | - |
dc.contributor.author | Ohta, Takehiro | - |
dc.contributor.author | Cho, Jaeheung | - |
dc.date.accessioned | 2023-12-21T17:14:03Z | - |
dc.date.available | 2023-12-21T17:14:03Z | - |
dc.date.created | 2020-09-03 | - |
dc.date.issued | 2020-07 | - |
dc.description.abstract | The importance of redox-inactive metal ions in modulating the reactivity of redox-active biological systems is a subject of great current interest. In this work, the effect of redox-inactive metal ions (M3+ = Sc3+, Y3+, Yb3+, La3+) on the nucleophilic reactivity of a mononuclear ligand-based alkylperoxocopper(II) complex, [Cu(Pr-i(2)-tren-C(CH3)(2)O-2)](+) (1), was examined. 1 was prepared by the addition of hydrogen peroxide and triethylamine to the solution of [Cu(Pr-i(3)-tren)(CH3CN)](+) (Pr-i(3)-tren = tris[2-(isopropylamino)ethyl]amine) via the formation of [Cu(Pr-i(3)-tren)(O2H)](+) (2) in methanol (CH3OH) at 30 degrees C. 1 was characterized using density functional theory (DFT) calculations and spectroscopic methods such as UV-vis, resonance Raman (rR), and electron paramagnetic resonance (EPR). DFT calculations support the electronic structure of 1 with an intermediate geometry between the trigonal-bipyramidal and square-pyramidal geometries, which is consistent with the observed EPR signal exhibiting a signal with g(perpendicular to) = 2.03 (A(perpendicular to) = 16 G) and g(parallel to) = 2.19 (A(parallel to) = 158 G). The Cu-O bond stretching frequency of 1 was observed at 507 cm(-1) for O-16(2) species (486 cm(-1) for O-18(2) species), and its O-O vibrational energy was determined to be 799 cm(-1) for O-16(2) species (759 cm(-1) for O-18(2) species) by rR spectroscopy. The reactivity of 1 was investigated in oxidative nucleophilic reactions. The positive slope of the Hammett plot (rho = 2.3(1)) with para-substituted benzaldehydes and the reactivity order with 1 degrees-, 2 degrees-, and 3 degrees-CHO demonstrate well the nucleophilic character of this copper(II) ligand-based alkylperoxo complex. The Lewis acidity of M3+ improves the oxidizing ability of 1. The modulated reactivity of 1 with M3+ was revealed to be an opposite trend of the Lewis acidity of M3+ in aldehyde deformylation. | - |
dc.identifier.bibliographicCitation | INORGANIC CHEMISTRY, v.59, no.14, pp.9938 - 9943 | - |
dc.identifier.doi | 10.1021/acs.inorgchem.0c01109 | - |
dc.identifier.issn | 0020-1669 | - |
dc.identifier.scopusid | 2-s2.0-85088121410 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/48086 | - |
dc.identifier.url | https://pubs.acs.org/doi/10.1021/acs.inorgchem.0c01109 | - |
dc.identifier.wosid | 000552287100047 | - |
dc.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | Redox-Inactive Metal Ions That Enhance the Nucleophilic Reactivity of an Alkylperoxocopper(II) Complex | - |
dc.type | Article | - |
dc.description.isOpenAccess | FALSE | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Inorganic & Nuclear | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | OXYGEN-EVOLVING COMPLEX | - |
dc.subject.keywordPlus | PHOTOSYSTEM-II | - |
dc.subject.keywordPlus | REACTION INTERMEDIATE | - |
dc.subject.keywordPlus | ELECTRON-TRANSFER | - |
dc.subject.keywordPlus | CRYSTAL-STRUCTURE | - |
dc.subject.keywordPlus | OXIDATION | - |
dc.subject.keywordPlus | LIGAND | - |
dc.subject.keywordPlus | ACTIVATION | - |
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