通过简便的铂-银协同催化策略将 5-HMF 高选择性氧化为 HMFCA

Ming-Kun Ke, Yuan Min, Shu-Chuan Mei, Hou-Wei Zeng, Zhao-Hua Wang, Tian-Wei Hua, Jie-Jie Chen, Gui-Xiang Huang, Han-Qing Yu
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引用次数: 0

摘要

5- 羟甲基-2-呋喃羧酸(HMFCA)是化工和制药行业的重要原料。通过 5-羟甲基糠醛(5-HMF)的有氧转化生产 HMFCA 具有广阔的前景,但却面临过度氧化的挑战。在这项工作中,我们开发了一种改进的铂-银协同催化策略,以调整 5-HMF 有氧氧化的选择性。通过在铂纳米颗粒热催化体系中简单地原位添加 AgNO,5-HMF 氧化的主要产物可以从 2,5-呋喃二甲酸(FDCA)转移到 HMFCA,其选择性超过 99%。密度泛函理论计算表明,这种策略可以将 HMFCA 的吸附位点从铂位点转移到银位点,从而防止羟甲基的氧化。此外,这种策略还可扩展到其他银物种,如 AgCl、AgO 和 AgO。这项工作为铂银协同催化提供了深入的见解,并为控制生物质提纯的产品选择性开辟了一条简单的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Highly selective oxidation of 5-HMF to HMFCA via a facile Pt-Ag co-catalytic strategy
5-Hydroxymethyl-2-furancarboxylic acid (HMFCA) is an important feedstock in chemical and pharmaceutical industries. Its production through aerobic conversion of 5-hydroxymethylfurfural (5-HMF) has promising prospects but is challenged by the over-oxidation. In this work, we develop a refined Pt-Ag co-catalytic strategy to tailor the selectivity of 5-HMF’s aerobic oxidation. By simple in situ addition of AgNO to the thermal catalytic system of Pt nanoparticles, the main products of 5-HMF oxidation could be shifted from 2,5-furandicarboxylic acid (FDCA) to HMFCA with an ultrahigh selectivity of over 99 %. Density functional theory calculations demonstrate that such strategy could alter the HMFCA adsorption sites from Pt to Ag sites and prevent the oxidation of hydroxymethyl group. In addition, this strategy can be extended to other Ag species, such as AgCl, AgO and AgO. This work provides insights into the Pt-Ag synergistic catalysis and opens up a simple avenue to control the product selectivity for biomass refinement.
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