4-OH-TEMPO radical grafted onto a novel polyaromatic ether sulfone containing carboxyl side chains as solid catalyst for alcohol oxidation

2,2,6,6-Tetramethylpiperidinium-nitroxide (TEMPO) is a mild and efficient catalyst, which is important in the industrial production of selective oxidation of alcohols to the corresponding aldehyde or ketone compounds. However, it is a challenge to recover the expensive TEMPO catalyst in homogeneous catalytic systems. In this study, a novel polymer-supported catalyst was prepared using 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxy (4-OH-TEMPO) and polyaromatic ether sulfone (PAES). The successful grafting of 4-OH-TEMPO in PAES-C was demonstrated by 1 H nuclear magnetic resonance ( 1 H NMR) and Fourier transform infrared (FT-IR), load capacity can be calculated by elemental analysis (EA). BET and scanning electron microscopy (SEM) to depict the structure-performance relationship. Herein, SEM images revealed the existence of porous structure. This structure can effectively adsorb NO molecules to form a PAES-TEMPO/NO x catalytic system to selectively oxidize benzyl alcohol. The experimental results indicated the high activity, the subsequent benzyl alcohol oxidation cycle can reach more than 93% conversion without showing a large loss of selectivity. More importantly, the as-prepared catalyst exhibited the attractive recyclability (recovery rate is 98%). After 10 consecutive runs, no significant loss of conversion and selectivity was observed (the conversion rate of benzyl alcohol was more than 93% and the selectivity was more than 95%). This study might provide some recommendation on the development of highly efficient catalysts for alcohol oxidation.