Matches in SemOpenAlex for { <https://semopenalex.org/work/W4307181150> ?p ?o ?g. }
- W4307181150 endingPage "17789" @default.
- W4307181150 startingPage "17777" @default.
- W4307181150 abstract "A series of azo-aromatic copper(II) complexes, [1a-g] and a Cu(I) complex, [1h], with varying amine-functionalized hemilabile pincer-like [HL1–3] and [L1,2], methyl-substituted azo [L3], and imine [L4] ligands, were synthesized and characterized. These complexes were investigated for aerobic oxidation of a variety of aromatic alcohols in the presence of 2.0 mol % precatalysts [1a-g], cobaltocene (2.0 mol %), N-methyl imidazole (NMI) (8.0 mol %), and TEMPOH (2.0 mol %) at room temperature. The Cu(I) complex (1h) acted as a catalyst in the absence of cobaltocene. To understand the mechanism, detailed experimental and theoretical studies have been performed with the representative complex [1a], which has suggested a new kind of mechanism involving a Cu(II)/Cu(I) redox couple. Cobaltocene acts as a reductant to [1a] to generate a Cu(I) complex, which activates dioxygen in the presence of NMI. TEMPOH transfers a hydrogen atom to the activated dioxygen with the generation of TEMPO•, which further participates in α-C–H bond activation in the Cu(II)-alkoxide intermediate in an intermolecular fashion in the catalytic cycle. The amine sidearm in the ligand backbone of the complexes has a significant role in catalytic activity. Complexes with amine sidearms are more effective than complexes without them. Moreover, the aliphatic secondary amine sidearm is more efficient among the amine sidearm than the aromatic secondary amine and tertiary amines. The amine sidearm that remained coordinated to the Cu(II) center is hemilabile, and it facilitates alcohol coordination in the catalytic process. Alcohol coordination was the rate-limiting step, and it was supported by the isotope effect study on benzyl alcohol, substitution effect on the amine moiety of the ligands, and DFT calculation. The hemilabile amine sidearm of the coordinated ligand also acted as a base in deprotonating the alcoholic O–H proton and acted as an acid in releasing H2O2 during the catalysis." @default.
- W4307181150 created "2022-10-29" @default.
- W4307181150 creator A5001464365 @default.
- W4307181150 creator A5006299703 @default.
- W4307181150 creator A5031979634 @default.
- W4307181150 creator A5032282584 @default.
- W4307181150 creator A5038774171 @default.
- W4307181150 creator A5060299295 @default.
- W4307181150 date "2022-10-24" @default.
- W4307181150 modified "2023-10-02" @default.
- W4307181150 title "Hemilabile Amine-Functionalized Efficient Azo-Aromatic Cu-Catalysts Inspired by Galactose Oxidase: Impact of Amine Sidearm on Catalytic Aerobic Oxidation of Alcohols" @default.
- W4307181150 cites W1981940760 @default.
- W4307181150 cites W1992749453 @default.
- W4307181150 cites W2014008543 @default.
- W4307181150 cites W2016231436 @default.
- W4307181150 cites W2017093537 @default.
- W4307181150 cites W2019974637 @default.
- W4307181150 cites W2025258396 @default.
- W4307181150 cites W2033020343 @default.
- W4307181150 cites W2044671255 @default.
- W4307181150 cites W2049367130 @default.
- W4307181150 cites W2065836316 @default.
- W4307181150 cites W2075626330 @default.
- W4307181150 cites W2077140551 @default.
- W4307181150 cites W2081048082 @default.
- W4307181150 cites W2085106254 @default.
- W4307181150 cites W2092202359 @default.
- W4307181150 cites W2098772094 @default.
- W4307181150 cites W2110592823 @default.
- W4307181150 cites W2132934971 @default.
- W4307181150 cites W2138710897 @default.
- W4307181150 cites W2151626815 @default.
- W4307181150 cites W2152919588 @default.
- W4307181150 cites W2171065938 @default.
- W4307181150 cites W2171892019 @default.
- W4307181150 cites W2213069300 @default.
- W4307181150 cites W2314357145 @default.
- W4307181150 cites W2314837838 @default.
- W4307181150 cites W2327847449 @default.
- W4307181150 cites W2335686433 @default.
- W4307181150 cites W2480134740 @default.
- W4307181150 cites W2484830969 @default.
- W4307181150 cites W2497677305 @default.
- W4307181150 cites W2521189477 @default.
- W4307181150 cites W2549933044 @default.
- W4307181150 cites W2563538756 @default.
- W4307181150 cites W2570368602 @default.
- W4307181150 cites W2589757617 @default.
- W4307181150 cites W2766725153 @default.
- W4307181150 cites W2806444024 @default.
- W4307181150 cites W2889854129 @default.
- W4307181150 cites W2899721320 @default.
- W4307181150 cites W2907887422 @default.
- W4307181150 cites W2949422348 @default.
- W4307181150 cites W2950812332 @default.
- W4307181150 cites W2951136847 @default.
- W4307181150 cites W2958375404 @default.
- W4307181150 cites W2970819209 @default.
- W4307181150 cites W3012831955 @default.
- W4307181150 cites W3017287986 @default.
- W4307181150 cites W3056739199 @default.
- W4307181150 cites W3216581333 @default.
- W4307181150 cites W402656947 @default.
- W4307181150 cites W4200400999 @default.
- W4307181150 cites W4252368097 @default.
- W4307181150 cites W4376043526 @default.
- W4307181150 doi "https://doi.org/10.1021/acs.inorgchem.2c03087" @default.
- W4307181150 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36278950" @default.
- W4307181150 hasPublicationYear "2022" @default.
- W4307181150 type Work @default.
- W4307181150 citedByCount "4" @default.
- W4307181150 countsByYear W43071811502023 @default.
- W4307181150 crossrefType "journal-article" @default.
- W4307181150 hasAuthorship W4307181150A5001464365 @default.
- W4307181150 hasAuthorship W4307181150A5006299703 @default.
- W4307181150 hasAuthorship W4307181150A5031979634 @default.
- W4307181150 hasAuthorship W4307181150A5032282584 @default.
- W4307181150 hasAuthorship W4307181150A5038774171 @default.
- W4307181150 hasAuthorship W4307181150A5060299295 @default.
- W4307181150 hasConcept C116569031 @default.
- W4307181150 hasConcept C131779359 @default.
- W4307181150 hasConcept C155647269 @default.
- W4307181150 hasConcept C161790260 @default.
- W4307181150 hasConcept C170493617 @default.
- W4307181150 hasConcept C178790620 @default.
- W4307181150 hasConcept C181199279 @default.
- W4307181150 hasConcept C185592680 @default.
- W4307181150 hasConcept C188027245 @default.
- W4307181150 hasConcept C2777438722 @default.
- W4307181150 hasConcept C2780874372 @default.
- W4307181150 hasConcept C3018358672 @default.
- W4307181150 hasConcept C55493867 @default.
- W4307181150 hasConcept C63338738 @default.
- W4307181150 hasConcept C75473681 @default.
- W4307181150 hasConceptScore W4307181150C116569031 @default.
- W4307181150 hasConceptScore W4307181150C131779359 @default.
- W4307181150 hasConceptScore W4307181150C155647269 @default.
- W4307181150 hasConceptScore W4307181150C161790260 @default.