Synthesis of new fluorinated imidazolium ionic liquids and their prospective function as the electrolytes for lithium-ion batteries

Two fluorine-containing ionic liquids, 1-(2,2,2-trifluoroethyl)-3-methylimidazolium tosylate and 1-(2,2,2-trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (TFSI anion), were obtained in good yields and high purity via a green pathway procedure free of solvent and hazardous cata...

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Veröffentlicht in:Journal of fluorine chemistry 2014-08, Vol.164, p.38-43
Hauptverfasser: Tran, Anh Ngoc, Van Do, Thanh-Nhan, Le, Loan-Phung My, Le, Thach Ngoc
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container_end_page 43
container_issue
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container_title Journal of fluorine chemistry
container_volume 164
creator Tran, Anh Ngoc
Van Do, Thanh-Nhan
Le, Loan-Phung My
Le, Thach Ngoc
description Two fluorine-containing ionic liquids, 1-(2,2,2-trifluoroethyl)-3-methylimidazolium tosylate and 1-(2,2,2-trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (TFSI anion), were obtained in good yields and high purity via a green pathway procedure free of solvent and hazardous catalyst. The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. The preliminary electrochemical results are very promising, a wide electrochemical stability up to 5.7V vs Li+/Li for the fluorinated imidazolium with TFSI anion. •Green pathway to prepare fluorinated ionic liquids.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium tosylate.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide.•Both will be prospective electrolytes for lithium batteries.•[CF3CH2MIm][Tf2N] even showed a wider electrochemical window. Two fluorine-containing ionic liquids, 1-(2,2,2-trifluoroethyl)-3-methylimidazolium tosylate and 1-(2,2,2-trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (TFSI anion), were obtained in good yields and high purity via a green pathway procedure free of solvent and hazardous catalyst. The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. The preliminary electrochemical results are very promising, a wide electrochemical stability up to 5.7V vs Li+/Li for the fluorinated imidazolium with TFSI anion.
doi_str_mv 10.1016/j.jfluchem.2014.05.005
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The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. The preliminary electrochemical results are very promising, a wide electrochemical stability up to 5.7V vs Li+/Li for the fluorinated imidazolium with TFSI anion. •Green pathway to prepare fluorinated ionic liquids.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium tosylate.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide.•Both will be prospective electrolytes for lithium batteries.•[CF3CH2MIm][Tf2N] even showed a wider electrochemical window. Two fluorine-containing ionic liquids, 1-(2,2,2-trifluoroethyl)-3-methylimidazolium tosylate and 1-(2,2,2-trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (TFSI anion), were obtained in good yields and high purity via a green pathway procedure free of solvent and hazardous catalyst. The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. 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The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. The preliminary electrochemical results are very promising, a wide electrochemical stability up to 5.7V vs Li+/Li for the fluorinated imidazolium with TFSI anion. •Green pathway to prepare fluorinated ionic liquids.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium tosylate.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide.•Both will be prospective electrolytes for lithium batteries.•[CF3CH2MIm][Tf2N] even showed a wider electrochemical window. Two fluorine-containing ionic liquids, 1-(2,2,2-trifluoroethyl)-3-methylimidazolium tosylate and 1-(2,2,2-trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (TFSI anion), were obtained in good yields and high purity via a green pathway procedure free of solvent and hazardous catalyst. The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. 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The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. The preliminary electrochemical results are very promising, a wide electrochemical stability up to 5.7V vs Li+/Li for the fluorinated imidazolium with TFSI anion. •Green pathway to prepare fluorinated ionic liquids.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium tosylate.•1-(2,2,2-Trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide.•Both will be prospective electrolytes for lithium batteries.•[CF3CH2MIm][Tf2N] even showed a wider electrochemical window. Two fluorine-containing ionic liquids, 1-(2,2,2-trifluoroethyl)-3-methylimidazolium tosylate and 1-(2,2,2-trifluoroethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (TFSI anion), were obtained in good yields and high purity via a green pathway procedure free of solvent and hazardous catalyst. The incorporation of CF3 moieties in imidazolium structure decreases the ILs TFSI melting point. The preliminary electrochemical results are very promising, a wide electrochemical stability up to 5.7V vs Li+/Li for the fluorinated imidazolium with TFSI anion.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.jfluchem.2014.05.005</doi><tpages>6</tpages></addata></record>
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subjects Anions
Electrochemical stability
Electrolyte
Electrolytes
Fluorinated imidazolium
Fluorination
Ionic liquids
Lithium
Lithium-ion batteries
Lithium-ion battery
Solvent-free pathway
Solvents
Synthesis (chemistry)
title Synthesis of new fluorinated imidazolium ionic liquids and their prospective function as the electrolytes for lithium-ion batteries
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