Tungsten-dioxo single-site heterogeneous catalyst on carbon: synthesis, structure, and catalysis†

IF 4.2 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2025-01-20 Epub Date: 2025-01-22 DOI:10.1039/d4cy01517g
Amol Agarwal , Yiqi Liu , Miyuki Hanazawa , Jiaqi Li , Takayuki Nakamuro , Eiichi Nakamura , Yosi Kratish , Tobin J. Marks
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Abstract

This study investigates the application of a novel third-row metal, tungsten, to carbon-supported single-site metal-oxo heterogeneous catalysis. Tungsten is a green and earth-abundant metal, but an unexplored candidate in this role. The carbon (AC = activated carbon)-supported tungsten dioxo complex, AC/WO2 was prepared via grafting of (DME)WO2Cl2 (DME = 1,2-dimethoxyethane) onto high-surface-area activated carbon. AC/WO2 was fully characterized by ICP-OES, XPS, EXAFS, XANES, SMART-EM, and DFT. W 4d7/2 XPS and W LIII-Edge XANES assign the oxidation state as W(vi), while EXAFS reveals two WO double and two W–O single bonds at distances of 1.73 and 1.92 Å, respectively. These data align well with DFT computational results, supporting the structure as Carbon(–μ-O–)2M(O)2. SMART-EM verifies that single W(vi) catalytic sites are bonded in an out-of-plane manner. The catalytic performance of air- and water-stable AC/WO2 is compared to that of AC/MoO2. AC/WO2 is more active and selective than the molybdenum analog in mediating alcohol dehydration of various substrates, and is recyclable. Notably, AC/WO2 is an effective and recyclable catalyst for primary aliphatic alcohol dehydration and forms no dehydrogenation side products in contrast to AC/MoO2. However, AC/WO2 is less effective in epoxidation and PET depolymerization. Overall, this work demonstrates the potential of carbon-supported third row metals for future studies.

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碳上钨-二氧基单位点多相催化剂:合成、结构和催化作用†
本研究探讨了一种新型的第三排金属钨在碳负载单点金属-氧非均相催化中的应用。钨是一种绿色且在地球上储量丰富的金属,但在这一角色中尚未被开发。通过在高表面积活性炭上接枝(DME)WO2Cl2 (DME = 1,2-二甲氧基乙烷),制备了碳(AC =活性炭)负载的钨二氧配合物AC/WO2。采用ICP-OES、XPS、EXAFS、XANES、SMART-EM和DFT对AC/WO2进行了表征。w4d7 /2 XPS和wliii - edge XANES将氧化态定位为W(VI),而EXAFS显示两个WO双键和两个W - o单键,距离分别为1.73和1.92 Å。这些数据与DFT计算结果吻合较好,支持碳(- μ-O -)2M(O)2的结构。SMART-EM验证了单个W(VI)催化位点以平面外的方式键合。比较了空气稳定和水稳定AC/WO2与AC/MoO2的催化性能。与钼类似物相比,AC/WO2在多种底物的醇脱水中具有更高的活性和选择性,并且可回收利用。值得注意的是,与AC/MoO2相比,AC/WO2是一种有效的、可回收的伯脂肪醇脱水催化剂,不会产生脱氢副产物。然而,AC/WO2在环氧化和PET解聚方面效果较差。总的来说,这项工作证明了碳负载的第三行金属在未来研究中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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