铁催化二氧化碳选择性氢化、硼氢化和硅氢化
Iron-Catalyzed Selective Hydrogenation and Hydroboration/Hydrosilylation of CO2
Received date: 2024-06-28
Revised date: 2024-07-27
Online published: 2024-08-26
赵秋婷 , 王文光 . 铁催化二氧化碳选择性氢化、硼氢化和硅氢化[J]. 有机化学, 2024 , 44(10) : 3106 -3116 . DOI: 10.6023/cjoc202405032
Carbon dioxide (CO2) serves as a sustainable carbon source for building biomass, fossil fuels, and organic chemicals. Converting CO2 into value-added chemicals or fuels is an ideal approach to achieve carbon cycling. The reduction and conversion of CO2, a pivotal aspect of C1 chemistry, have long been a subject of intense research interest. Previous studies have demonstrated that through transition metal catalysis, hydrogen, boranes, and silanes (E—H, E=H, B or Si) act as effective reducing agents to transform CO2 into a range of C1 chemicals, such as formate, formaldehyde, and methanol. Over the past decade, research focus in this field has shifted towards utilizing cost-effective metals as catalysts for selective CO2 reduction. A comprehensive review of homogeneous iron-catalyzed CO2 reduction using E—H is presented, emphasizing reaction mechanisms and selectivity.
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