期刊
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 2022, 期 35, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.202200509
关键词
Catalysis; Copper; Dinuclear Complex; Ligand Rigidity; Tyrosinase
资金
- CAU Kiel
- Projekt DEAL
In this study, four structurally related bis-tridentate N-donor ligands with different functionalities were synthesized to form corresponding dicopper(I) complexes as catalysts for the conversion of 2,4-di-tert-butylphenol. The results showed evidence of a mu-eta(2):eta(2)-peroxo-dicopper(II) species and catalytic conversion in the imine ligand systems but not in the amine ligand systems.
Four structurally related bis-tridentate N-donor ligands with either two secondary amine or two imine functions were synthesized, and the corresponding dicopper(I) complexes were investigated as catalysts for the tyrosinase-like conversion of 2,4-di-tert-butylphenol (DTBP-H) to 3,5-di-tert-butylquinone (DTBQ). Notably, the imine systems show evidence for both a mu-eta(2):eta(2)-peroxo-dicopper(II) species and catalytic conversion of DTBP-H to DTBQ. Moreover, kinetic studies indicate that a dinuclear copper-oxygen species is involved in the monooxygenation of DTBP-H. In contrast, the amine systems do not show monooxygenase activity. Comparison of the experimentally determined catalytic activities with DFT-optimized geometries of mu-eta(2):eta(2)-peroxo-dicopper(II) intermediates suggests that the ligand rigidity of the imine systems allows equatorial attack of the substrate and, thus, subsequent monooxygenation whereas this is not possible in the amine systems due to the fact that no free equatorial positions are available in the mu-peroxo intermediate.
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