Ardemani Leandro, Cibin Giannantonio, Dent Andrew J, Isaacs Mark A, Kyriakou Georgios, Lee Adam F, Parlett Christopher M A, Parry Stephen A, Wilson Karen
European Bioenergy Research Institute , Aston University , Birmingham B4 7ET , UK . Email:
Diamond Light Source , Harwell Science and Innovation Campus , Didcot OX11 0DE , UK.
Chem Sci. 2015 Aug 1;6(8):4940-4945. doi: 10.1039/c5sc00854a. Epub 2015 Jun 8.
Nanoparticulate gold has emerged as a promising catalyst for diverse mild and efficient selective aerobic oxidations. However, the mechanism of such atom-economical transformations, and synergy with functional supports, remains poorly understood. Alkali-free Mg-Al hydrotalcites are excellent solid base catalysts for the aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furan dicarboxylic acid (FDCA), but only in concert with high concentrations of metallic gold nanoparticles. In the absence of soluble base, competitive adsorption between strongly-bound HMF and reactively-formed oxidation intermediates site-blocks gold. Aqueous NaOH dramatically promotes solution phase HMF activation, liberating free gold sites able to activate the alcohol function within the metastable 5-hydroxymethyl-2-furancarboxylic acid (HMFCA) reactive intermediate. Synergistic effects between moderate strength base sites within alkali-free hydrotalcites and high gold surface concentrations can afford highly selective and entirely heterogeneous catalysts for aqueous phase aldehyde and alcohol cascade oxidations pertinent to biomass transformation.
纳米金已成为一种有前景的催化剂,可用于多种温和且高效的选择性有氧氧化反应。然而,这种原子经济转化的机制以及与功能性载体的协同作用仍知之甚少。无碱的镁铝水滑石是将5-羟甲基糠醛(HMF)有氧氧化为2,5-呋喃二甲酸(FDCA)的优良固体碱催化剂,但仅在与高浓度金属金纳米颗粒协同作用时才有效。在没有可溶性碱的情况下,强结合的HMF与反应形成的氧化中间体之间的竞争性吸附会阻断金的活性位点。氢氧化钠水溶液显著促进溶液相HMF的活化,释放出能够活化亚稳的5-羟甲基-2-呋喃甲酸(HMFCA)反应中间体中醇官能团的游离金位点。无碱水滑石中中等强度碱性位点与高金表面浓度之间的协同效应可为与生物质转化相关的水相醛和醇级联氧化反应提供高选择性且完全非均相的催化剂。