常压下异丙醇催化CO2转移加氢制甲酸的研究

IF 4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2024-12-16 Epub Date: 2025-01-02 DOI:10.1039/d4cy01329h
Tushar Singh , Subrata Chakraborty
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引用次数: 0

摘要

在这里,我们提出了地球上丰富的三维金属催化环境压力二氧化碳转移加氢生成甲酸的第一个例子,使用异丙醇作为一种廉价且环保的氢源。在130°C的THF: H2O混合物中,在1bar CO2条件下,双牙膦双(二苯基膦)丙烷(DPPP, βn = 91°)衍生的低价Cr(0)配合物Cr(DPPP)(CO)4C-3是最有效的催化剂,在NaOH存在下,在1bar CO2条件下,生成的甲酸钠的TON可达1974,在5bar CO2条件下,生成的TON可达2231。该催化剂在碳酸氢钠和碳酸盐的转移加氢反应中也很活跃,以低收率生产相应的甲酸盐。机理实验揭示了阴离子氢化物络合物的形成,这被认为是CO2转移氢化的活性催化剂。
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Chromium-catalyzed transfer hydrogenation of CO2 to formate using isopropanol under ambient pressure†
Herein, we present the first example of earth-abundant 3d metal-catalyzed ambient pressure carbon dioxide transfer hydrogenation to formate using isopropanol as an inexpensive and environmentally benign hydrogen source. The bidentate phosphine bis(diphenylphosphino)propane (DPPP, βn = 91°)-derived low-valent Cr(0) complex Cr(DPPP)(CO)4C- emerged as the most efficient catalyst yielding sodium formate with a TON of up to 1974 under 1 bar CO2 and 2231 under 5 bar CO2 in the presence of NaOH in a THF : H2O mixture after 24 h at 130 °C. The catalyst was also found to be active in the transfer hydrogenation of sodium bicarbonate and carbonate to produce their corresponding formates in low yields. Mechanistic experiments revealed formation of an anionic hydride complex, which is believed to be an active catalyst for CO2 transfer hydrogenation.
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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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