首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Syntheses,structures and properties of l-ethyl-3-methyI-imidazolium salts of fluorocomplex anions
【24h】

Syntheses,structures and properties of l-ethyl-3-methyI-imidazolium salts of fluorocomplex anions

机译:氟络合物阴离子的1-乙基-3-甲基I-咪唑鎓盐的合成,结构和性质

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Fluoroacid base reactions of a room-temperature ionic liquid,l-ethyl-3-methylimidazolium fluorohydrogenate (EMIm(HF)_(2.3)F,EMIm = l-ethyl-3-methylimidazolium cation),and Lewis fluoroacids (BF_3.PF_5,AsF_5,NbF_5,TaF_5 and WF_6) give EMIm salts of the corresponding fluorocomplex unions,EMImBF_4.EMImPF_6,EMImAsF_6,EMImNbF_6,EMImTaF,and EMImWF_7,respectively.Attempts to prepare EMImVF_6 by both the acid base reaction of EMIm(HF)_(2.3) F with VF_5 and the metathesis of EMImCl with KVF_6 failed due to the strong oxidizing power of the pentavalent vanadium,whereas EMImSbF_6 was successfully prepared only by the metathesis of EMImCl and KSbF_6.EMImBF_4,EMImSbF_6,EMImNbF,.EMInVTaF_6 and EMImWF_7 are liquids at room temperature whereas EMImPF_6 and EMImAsF_6 melts at around 330 K.Raman spectra of the obtained salts showed the existence of the EMIm cation and corresponding fluorocomplex anions.IR spectroscopy revealed that strong hydrogen bonds are not observed in these salts.EMImAsF,(mp 326 K) and EMImSbF_6 (mp 283 K) are isostructural with the previously reported EMImPF_6.The melting point of the hexafluorocomplex EMIm salt decreases with the increase of the size of the anion (PF_6~-
机译:室温离子液体,氟乙基1-甲基-3-甲基咪唑鎓盐(EMIm(HF)_(2.3)F,EMIm =乙基乙基-3-甲基咪唑鎓阳离子)和路易斯氟酸(BF_3.PF_5, AsF_5,NbF_5,TaF_5和WF_6)分别给出相应氟络合物的EMIm盐EMImBF_4.EMImPF_6,EMImAsF_6,EMImNbF_6,EMImTaF和EMImWF_7。 )由于五价钒的强氧化能力,导致VF_5的F和EMImCl与KVF_6的复分解失败,而EMImSbF_6仅通过EMImCl和KSbF_6的复分解才能成功制备.EMImBF_4,EMImSbF_6,EMImVTbF_6 at室温下,EMImPF_6和EMImAsF_6在约330 K时熔化。所得盐的拉曼光谱表明存在EMIm阳离子和相应的氟络合物阴离子。红外光谱表明在这些盐中未观察到强氢键.EMImAsF,(mp 326 K )和EMImSbF_6(mp 283 K)与先前报道的EMImPF_6是同构的。六氟配合物EMIm盐的熔点随阴离子尺寸的增加而降低(PF_6〜-

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号