4.6 Article

Application of optically active chiral bis-(imidazolium) salts as potential receptors of chiral dicarboxylate salts of biological relevance

期刊

ORGANIC & BIOMOLECULAR CHEMISTRY
卷 13, 期 19, 页码 5450-5459

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ob00348b

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  1. Ministerio de Economia y Competitividad [CTQ2011-28903-C02-01, CTQ2012-38543-C03-01]
  2. Generalitat Valenciana [PROMETEO 2012/020, ACCOMP/2014/275]
  3. Universitat Jaume I [P1.1B2013-38]

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A family of chiral bis(imidazolium) salts derived from natural amino acids has been synthesized by a simple synthetic approach and the corresponding bis(trifluoromethylsulfonyl) imide salts have been shown to be room temperature chiral ionic liquids (RTCILs). The structures and self-assembling properties of the resulting salts have been studied by (HNMR)-H-1, ATR-FTIR, DSC, SEM and theoretical calculations. Moreover, these receptors have been applied to the enantiomeric recognition of dicarboxylic amino acids. The supramolecular complexes formed have been studied by (HNMR)-H-1 titration experiments, ATR-FTIR and DSC.

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