Research Progress Regarding Transition Metal-Catalyzed Carbonylations with CO2/H-2
2021-05-15
发表期刊物理化学学报
ISSN1000-6818
卷号37期号:5页码:#VALUE!
发表状态已发表
DOI10.3866/PKU.WHXB202009098
摘要

Ever-increasing energy demands due to rapid industrialization and urban population growth have drastically reduced petroleum reserves and increased greenhouse-gas production, and the latter has consequently contributed to climate change and environmental damage. Therefore, it highly desirable to produce fuels and chemicals from non-petroleum feedstocks and to reduce the atmospheric concentrations of greenhouse gases. One solution has involved using carbon dioxide (CO2), a main greenhouse gas, as a C1 feedstock for producing industrial fuels and chemicals. However, this requires high energy input from reductants or reactants with relatively high free energy (e.g., H-2 gas) because CO2 is a highly oxidized, thermodynamically stable form of carbon. H-2 can be generated through water photolysis, making it an ideal reductant for hydrogenating CO2 to CO. In situ generation of CO such as this has been developed for various carbonylation reactions that produce high value-added chemicals and avoid deriving CO from fossil fuels. This is beneficial because CO is toxic, and when extracted from fossil fuels it requires tedious separation and transportation. This combination of CO2 and H-2 allows for functional molecules to be synthesized as entries into the chemical industry value chain and would generate a carbon footprint much lower than that of conventional petrochemical pathways. Based on this, CO2/H-2 carbonylations using homogeneous transition metal-based catalysts have attracted increasing attention. Through this process, alkenes have been converted to alcohols, carboxylic acids, amines, and aldehydes. Heterogeneous catalysis has also provided an innovative approach for the carbonylation of alkenes with CO2/H-2. Based on these alkene carbonylations, the scope of CO2/H-2 carbonylations has been expanded to include aryl halides, methanol, and methanol derivatives, which give the corresponding aryl aldehyde, acetic acid, and ethanol products. These carbonylations revealed indirect CO2-HCOOH-CO pathways and direct CO2 insertion pathways. The use of this process is ever-increasing and has expanded the scope of CO2 utilization to produce novel, high value-added or bulk chemicals, and has promoted sustainable chemistry. This review summarizes the recent advances in transition-metal-catalyzed carbonylations with CO2/H-2 and discusses the perspectives and challenges of further research.

关键词Carbon dioxide hydrogenation Carbonylation Transition metal catalysis Alcohols Aldehydes Carboxylic acids Ethanol Acetic acid
收录类别SCI ; SCIE ; 北大核心
语种中文
WOS研究方向Chemistry
WOS类目Chemistry, Physical
WOS记录号WOS:000616614800016
出版者PEKING UNIV PRESS
WOS关键词CARBON-DIOXIDE ; ACETIC-ACID ; CO2 HYDROGENATION ; DIRECT CONVERSION ; CARBOXYLIC-ACIDS ; ARYL BROMIDES ; METHANOL HYDROCARBOXYLATION ; EFFICIENT SYNTHESIS ; INTERNAL ALKENES ; LOWER OLEFINS
原始文献类型Review
引用统计
文献类型期刊论文
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/125702
专题物质科学与技术学院_硕士生
物质科学与技术学院_特聘教授组_孙予罕组
物质科学与技术学院_博士生
通讯作者Wang, Hui; Sun, Yuhan
作者单位
1.Chinese Acad Sci, Shanghai Adv Res Inst, CAS Key Lab Low Carbon Convers Sci & Engn, Shanghai 201203, Peoples R China;
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China;
3.ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201203, Peoples R China;
4.Shanghai Inst Clean Technol, Shanghai 201620, Peoples R China
通讯作者单位物质科学与技术学院
推荐引用方式
GB/T 7714
Hua, Kaimin,Liu, Xiaofang,Wei, Baiyin,et al. Research Progress Regarding Transition Metal-Catalyzed Carbonylations with CO2/H-2[J]. 物理化学学报,2021,37(5):#VALUE!.
APA Hua, Kaimin,Liu, Xiaofang,Wei, Baiyin,Zhang, Shunan,Wang, Hui,&Sun, Yuhan.(2021).Research Progress Regarding Transition Metal-Catalyzed Carbonylations with CO2/H-2.物理化学学报,37(5),#VALUE!.
MLA Hua, Kaimin,et al."Research Progress Regarding Transition Metal-Catalyzed Carbonylations with CO2/H-2".物理化学学报 37.5(2021):#VALUE!.
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