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The catalytic properties of in situ formed copper(II) complexes of N,N,N′,N′-tetramethylethylenediamine (TMEDA), rac-1,2-diaminocyclohexane (DACH) and 9,10-diaminophenantrene (DAPHEN) were investigated under optimized reaction conditions in the oxidation of veratryl alcohol (3,4-dimethoxybenzyl alcohol) with molecular oxygen in alkaline aqueous solutions. The kinetics of the reaction, catalytic species and their deactivation were studied, in order to clarify the reasons for low conversions in Cu(TMEDA) and Cu(DACH) catalyzed reactions. The most active catalyst was the scarcely soluble Cu(DAPHEN) with turn over number 5700 in the oxidation of veratryl alcohol. The catalytic precursors in Cu(TMEDA) catalyzed reactions is binuclear hydroxyl bridged complex (LCu-μ-(OH)2-CuL)2+. The main reason for the deactivation of these catalysts according to our results is the reactivity of the ligands under reaction conditions.

Cobalt salen-type [salen= N , N ′-bis(salicylidene)ethylenediamine] complexes 1 – 6 were studied as catalysts for dioxygen activation in the oxidation of veratryl alcohol in basic aqueous conditions. The complexes Co(salen) ( 1 ), Co(αCH 3 salen) ( 2 ) [αCH 3 salen= N , N ′-bis(αmethylsalicylidene)ethylenediamine], Co(4OHsalen) ( 3 ) [4OHsalen= N , N ′-bis(4-hydroxosalicylidene)ethylenediamine], Co(sulfosalen) ( 4 ) [sulfosalen= N , N ′-bis(5-sulfonatosalicylidene)ethylenediamine], Co(acacen) ( 5 ) [acacen= N , N ′-bis(acetylacetone)ethylenediamine) and Co(N-Me-salpr) ( 6 ) [N-Me-salpr=bis(salicylideniminato-3-propyl)methylamine] were chosen to examine the influence of ligand structure on the catalytic activity. The effect of reaction conditions on the oxidation of veratryl alcohol was studied by varying temperature, pH, time or the nature and amount of the axial base needed to enhance the activity of complexes 1 – 5 . The catalytic behaviour of the studied complexes was shown to be very depended on the applied conditions and distinct differences could be observed among the complexes. In all reactions, veratraldehyde was the only product observed. The unsubstituted complex 1 was the most efficient catalyst in the studied system achieving turnover numbers of up to 28 at 80 °C and pH 12.5.