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dc.contributor.authorVermaak, Vincent
dc.contributor.authorYoung, Desmond A.
dc.contributor.authorSwarts, Andrew J.
dc.identifier.citationVermaak, V. et al. 2018. Catalytic oxidation of alcohols with novel non-heme N4-tetradentate manganese(II) complexes. Dalton transactions, 47(46):16534-16542. []en_US
dc.identifier.issn1477-9234 (Online)
dc.description.abstractWe report the preparation and characterisation of a series of novel non-heme N4-tetradentate Mn(OTf)2 complexes of the type, [(L)MnOTf2], where L = R,R and S,S enantiomers of BPMCN, its 6-methyl and 6-bromo derivatives as well as the novel ligand BMIMCN (BPMCN = N,N′-dimethyl-N,N′-bis(2-pyridylmethyl)-(R,R/S,S)-1,2-diaminocyclohexane, BMIMCN = N,N′-dimethyl-N,N′-bis(1-methyl-2-imidazolemethyl)-(R,R/S,S)-1,2-diaminocyclohexane). Solid state structural analysis of the BMIMCN-ligated Mn-triflate complexes (R,R-C4 and S,S-C4) revealed opposite helicity but identical metal site accessibility. This feature was exploited in the catalytic oxidation of primary and secondary alcohols, with hydrogen peroxide as oxidant and acetic acid as co-catalyst. Complexes R,R-C4 and S,S-C4 displayed the highest activity in benzyl alcohol oxidation, attributed to the electron-donating property of the BMIMCN ligand. Complex S,S-C4, displayed high activity for a variety of primary alcohol substrates, but the reaction suffered from reduced selectivity and side-reactions due to the presence of acetic acid. In contrast, secondary alcohol substrates could be oxidised to the corresponding ketone products in excellent isolated yields under mild reaction conditions and short reaction timesen_US
dc.titleCatalytic oxidation of alcohols with novel non-heme N4-tetradentate manganese(II) complexesen_US
dc.contributor.researchID24113883 - Vermaak, Vincent
dc.contributor.researchID23297573 - Young, Desmond Austin
dc.contributor.researchID25759949 - Swarts, Andrew John

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