A novel and facile method for selective ortho-C--H monofluorination of aniline derivatives was achieved using Selectfluor/Cu（OAc）JHOAc system. The reaction proceeded via electrophilic process with diverse substrates...A novel and facile method for selective ortho-C--H monofluorination of aniline derivatives was achieved using Selectfluor/Cu（OAc）JHOAc system. The reaction proceeded via electrophilic process with diverse substrates in acceptable moderate to high yields. The position selectivity was controlled by bidentate coordination of picolinic acid amides with copper.展开更多
Ethyl acetate (EA) shows low viscosity for its relative permittivity. Monofluorinated organic solvents exert the polar effect on the various properties. We have investigated the effect of position isomerism on the phy...Ethyl acetate (EA) shows low viscosity for its relative permittivity. Monofluorinated organic solvents exert the polar effect on the various properties. We have investigated the effect of position isomerism on the physical and electrochemical properties of two monofluorinated carboxylates: 2-fluoroethyl acetate (2FEA) and ethyl fluoroacetate (EFA). Relative permittivity of 2FEA was lower than that of EFA, whereas viscosity of 2FEA was higher. Electrolytic conductivity of a LiPF6 solution in 2FEA was lower than that in EFA, but higher than that in EA at high temperatures. The use of 2FEA as a co-solvent improved cycling efficiency and suppressed fading of discharge capacity of a Li|LiCoO2 coin cell at high cycle numbers.展开更多
Selective functionalization of C-F bonds in trifluoromethyl groups has recently received a growing interest, as it offers atom- and step-economic pathways to access highly valuable mono- and difluoroalkyl-substituted ...Selective functionalization of C-F bonds in trifluoromethyl groups has recently received a growing interest, as it offers atom- and step-economic pathways to access highly valuable mono- and difluoroalkyl-substituted organic molecules using simple and inexpensive trifluoromethyl sources as the starting materials. In this regard, impressive progress has been made on the defluorinative functionalization reactions that proceed via radical intermediates. Nevertheless, it is still a great challenge to precisely control the defluorination process, due to the continuous decrease of the C-F bond strength after the replacement of one or two fluorine atoms with various functionalities. This review article is aimed to provide a brief overview of recently reported methods used to functionalize C-F bonds of CF_(3) groups via radical intermediates. An emphasis is placed on the discussion of mechanistic aspects and synthetic applications.展开更多
文摘A novel and facile method for selective ortho-C--H monofluorination of aniline derivatives was achieved using Selectfluor/Cu（OAc）JHOAc system. The reaction proceeded via electrophilic process with diverse substrates in acceptable moderate to high yields. The position selectivity was controlled by bidentate coordination of picolinic acid amides with copper.
文摘Ethyl acetate (EA) shows low viscosity for its relative permittivity. Monofluorinated organic solvents exert the polar effect on the various properties. We have investigated the effect of position isomerism on the physical and electrochemical properties of two monofluorinated carboxylates: 2-fluoroethyl acetate (2FEA) and ethyl fluoroacetate (EFA). Relative permittivity of 2FEA was lower than that of EFA, whereas viscosity of 2FEA was higher. Electrolytic conductivity of a LiPF6 solution in 2FEA was lower than that in EFA, but higher than that in EA at high temperatures. The use of 2FEA as a co-solvent improved cycling efficiency and suppressed fading of discharge capacity of a Li|LiCoO2 coin cell at high cycle numbers.
基金National Natural Science Foundation of China (No.21971226)the Fundamental Research Funds for the Central Universities (No. WK2060000017) for financial support。
文摘Selective functionalization of C-F bonds in trifluoromethyl groups has recently received a growing interest, as it offers atom- and step-economic pathways to access highly valuable mono- and difluoroalkyl-substituted organic molecules using simple and inexpensive trifluoromethyl sources as the starting materials. In this regard, impressive progress has been made on the defluorinative functionalization reactions that proceed via radical intermediates. Nevertheless, it is still a great challenge to precisely control the defluorination process, due to the continuous decrease of the C-F bond strength after the replacement of one or two fluorine atoms with various functionalities. This review article is aimed to provide a brief overview of recently reported methods used to functionalize C-F bonds of CF_(3) groups via radical intermediates. An emphasis is placed on the discussion of mechanistic aspects and synthetic applications.
