Defective Auδ−-Ov interfacial sites boost C-H bond activation for enhanced selective oxidation of amino alcohols to amino acids

Designing efficient active sites to facilitate the oxidation of hydroxyl group to carboxylic acid under the influence of nitrogen-containing functional groups is worth exploring, but it is rarely investigated. Herein, we construct defective Au-ZrO 2 interfacial structures by tuning the calcination temperature of ZrO 2 support to boost the oxidation of amino alcohols to amino acids. Interestingly, the modification of calcination temperature induces the escape of saturated coordination oxygen atoms in ZrO 2 support, leaving behind abundant surface oxygen vacancy (O v ). The as-formed Au δ− -O v interfacial site displays the unique synergistic adsorption effect and electron transfer ability. Specifically, the O v site voluntarily adsorbs the –NH 2 group of amino alcohol, thus ensuring that the electron-rich Au δ− nearby O v site adsorbs the hydroxyl groups and activates the C-H bond activation of NH 2 CH 2 CH 2 O* intermediates. Consequently, Au/ZrO 2 -600 catalyst with more defective Au δ− -O v interfacial sites exhibits 98.8 % product yield for the oxidation of diethanolamine to iminodiacetic acid at only 30 °C. The catalyst system is further extended to the oxidation of other amino alcohols, involving monoethanolamine and triethanolamine, to their corresponding amino acids with excellent catalytic performance.