摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-ethyl-N,N,N-tris(2-methoxyethyl)ammonium bis(trifluoromethanesulfonyl)imide | 1234576-73-8

中文名称
——
中文别名
——
英文名称
N-ethyl-N,N,N-tris(2-methoxyethyl)ammonium bis(trifluoromethanesulfonyl)imide
英文别名
——
N-ethyl-N,N,N-tris(2-methoxyethyl)ammonium bis(trifluoromethanesulfonyl)imide化学式
CAS
1234576-73-8
化学式
C2F6NO4S2*C11H26NO3
mdl
——
分子量
500.481
InChiKey
WXLUUGQJTRWIIH-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为产物:
    描述:
    bis(trifluoromethane)sulfonimide lithium 为溶剂, 以89%的产率得到N-ethyl-N,N,N-tris(2-methoxyethyl)ammonium bis(trifluoromethanesulfonyl)imide
    参考文献:
    名称:
    Ionic liquid electrolytes based on multi-methoxyethyl substituted ammoniums and perfluorinated sulfonimides: Preparation, characterization, and properties
    摘要:
    New functionalized ionic liquids (ILs), comprised of multi-methoxyethyl substituted quaternary ammonium canons (i.e. [N(CH2CH2OCH3)(4-n)(R)(n)](+) : n=1, R=CH3OCH2CH2; n=1, R=CH3, CH2CH3: n=2, R=CH3CH2), and two representative perfluorinated sulfonimide anions (i.e. bis(fluorosulfonyl)imide (FSI-) and bis(trifluoromethanesulfonyl)imide (TFSI-)), were prepared. Their fundamental properties, including phase transition, thermal stability, viscosity, density, specific conductivity and electrochemical window, were extensively characterized. These multi-ether functionalized ionic liquids exhibit good capability of dissolving lithium salts. Their binary electrolytes containing high concentration of the corresponding lithium salt ([Li+] >1.6 mol kg(-1)) show Li+ ion transference number (t(Li+)) as high as 0.6-0.7. Their electrochemical stability allows Li deposition/stripping realized at room temperature. The desired properties of these multi-ether functionalized ionic liquids make them potential electrolytes for Li (or Li-ion) batteries. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.electacta.2010.06.063
点击查看最新优质反应信息