Utievskyi Yurii, Neumann Christof, Sindlinger Julia, Schutjajew Konstantin, Oschatz Martin, Turchanin Andrey, Ueberschaar Nico, Schacher Felix H
Institute of Organic Chemistry and Macromolecular Chemistry, Friedrich Schiller University Jena, Humboldtstraße 10, 07743 Jena, Germany.
Institute of Physical Chemistry, Friedrich Schiller University Jena, Lessingstraße 10, 07743 Jena, Germany.
Nanomaterials (Basel). 2023 Sep 5;13(18):2498. doi: 10.3390/nano13182498.
Herein, we present a new heterogeneous catalyst active toward glucose to formic acid methyl ester oxidation. The catalyst was fabricated via electrostatic immobilization of the inorganic polyoxometalate HPA-5 catalyst H[PMoVO] onto the pore surface of amphiphilic block copolymer membranes prepared via non-solvent-induced phase separation (NIPS). The catalyst immobilization was achieved via wet impregnation due to strong coulombic interactions between protonated tertiary amino groups of the polar poly(2-(dimethylamino)ethyl methacrylate) block and the anionic catalyst. Overall, three sets of five consecutive catalytic cycles were performed in an autoclave under 90 °С and 11.5 bar air pressure in methanol, and the corresponding yields of formic acid methyl ester were quantified via head-space gas chromatography. The obtained results demonstrate that the membrane maintains its catalytic activity over multiple cycles, resulting in high to moderate yields in comparison to a homogeneous catalytic system. Nevertheless, presumably due to leaching, the catalytic activity declines over five catalytic cycles. The morphological and chemical changes of the membrane during the prolonged catalysis under harsh conditions were examined in detail using different analytic tools, and it seems that the underlying block copolymer is not affected by the catalytic process.
在此,我们展示了一种对葡萄糖到甲酸甲酯氧化具有活性的新型多相催化剂。该催化剂是通过将无机多金属氧酸盐HPA - 5催化剂H[PMoVO]通过静电固定在经非溶剂诱导相分离(NIPS)制备的两亲性嵌段共聚物膜的孔表面上而制备的。由于极性聚(甲基丙烯酸2 - (二甲基氨基)乙酯)嵌段的质子化叔氨基与阴离子催化剂之间存在强库仑相互作用,通过湿浸渍实现了催化剂的固定化。总体而言,在高压釜中于90℃和11.5巴空气压力下在甲醇中进行了三组五次连续催化循环,并通过顶空气相色谱法定量了相应的甲酸甲酯产率。所得结果表明,该膜在多个循环中保持其催化活性,与均相催化体系相比,产率高至中等。然而,可能由于浸出,催化活性在五个催化循环后下降。使用不同的分析工具详细研究了在苛刻条件下长时间催化过程中膜的形态和化学变化,似乎基础嵌段共聚物不受催化过程的影响。