Preparation of amino acid chiral ionic liquid and visual chiral recognition of glutamine and phenylalanine enantiomers

被引:0
|
作者
Dong, Luzheng [1 ]
Wu, Jun [1 ]
Zhu, Xiashi [1 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, Guangling Coll, Yangzhou 225002, Peoples R China
基金
中国国家自然科学基金;
关键词
amino acids; chiral ionic liquids; enantioselective precipitate; recognition mechanism; visual chiral recognition; STABILITY; DOTS;
D O I
10.1002/chir.23665
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this paper, the amino acid chiral ionic liquid (AACIL) was prepared with L-phenylalanine and imidazole. It was characterized by CD, FT-IR, 1H NMR, and 13C NMR spectrum. The chiral recognition sensor was constructed with AACIL and Cu(II), which exhibited different chiral visual responses (solubility or color difference) to the enantiomers of glutamine (Gln) and phenylalanine (Phe). The effects of solvent, pH, time, temperature, metal ions, and other amino acids on visual chiral recognition were optimized. The minimum concentrations of Gln and Phe for visual chiral recognition were 0.20 mg/ml and 0.28 mg/ml, respectively. The mechanism of chiral recognition was investigated by FT-IR, TEM, SEM, TG, XPS, and CD. The location of the host-guest inclusion or molecular placement has been conformationally searched based on Gaussian 09 software. Amino acid chiral ionic liquid(AACIL) was successfully prepared and applied as a chiral recognition sensor. The sensor was applied for visual chiral recognition of the enantiomers of glutamine and phenylalanine, and the recognition conditions were optimized. Various methods are used to explore the mechanism of chiral recognition. image
引用
收藏
页数:13
相关论文
共 50 条
  • [21] Chiral separation of enantiomers of amino acid derivatives by HPLC on vancomycin and teicoplanin chiral stationary phases
    Lehotay, J
    Hrobonová, K
    Krupcík, J
    Cizmárik, J
    PHARMAZIE, 1998, 53 (12): : 863 - 865
  • [22] Separation of amino acid enantiomers VIA chiral derivatization and non-chiral gas chromatography
    Bertrand, Marylene
    Chabin, Annie
    Brack, Andre
    Westall, Frances
    JOURNAL OF CHROMATOGRAPHY A, 2008, 1180 (1-2) : 131 - 137
  • [23] Separation of amino acid enantiomers using supported liquid membrane extraction with chiral phosphates and phosphonates
    Dzygiel, P
    Wieczorek, P
    Jonsson, JÅ
    Milewska, M
    Kafarski, P
    TETRAHEDRON, 1999, 55 (32) : 9923 - 9932
  • [24] New chiral crown ether stationary phase for the liquid chromatographic resolution of α-amino acid enantiomers
    Hyun, MH
    Han, SC
    Lipshutz, BH
    Shin, YJ
    Welch, CJ
    JOURNAL OF CHROMATOGRAPHY A, 2001, 910 (02) : 359 - 365
  • [25] Chiral derivatizations applied for the separation of unusual amino acid enantiomers by liquid chromatography and related techniques
    Ilisz, Istvan
    Aranyi, Anita
    Peter, Antal
    JOURNAL OF CHROMATOGRAPHY A, 2013, 1296 : 119 - 139
  • [26] Maltodextrin-starch chiral composite membranes: Preparation, enantioselective recognition of phenylalanine and ibuprofen enantiomers, and molecular docking simulation
    Salehpour, Niloofar
    Nojavan, Saeed
    JOURNAL OF MEMBRANE SCIENCE, 2025, 717
  • [27] Visual chiral recognition of aromatic amino acids with (S)-mandelic acid-based ionic liquids via complexation
    Ma, Xiaofei
    Du, Yingxiang
    Zhu, Xinqi
    Yang, Jiangxia
    TALANTA, 2020, 217
  • [28] Enantioselective liquid-liquid extraction of 2-cyclohexylmandelic acid enantiomers using chiral ionic liquids
    Luo, Yachun
    Deng, Xiaoyu
    Zhang, Yan
    Sun, Genlin
    Yan, Zhihong
    CHIRALITY, 2024, 36 (06)
  • [29] A fluorescent chiral chemosensor for the recognition of the two enantiomers of chiral carboxylates
    Li, Yinan
    Tamilavan, Vellaiappillai
    Hyun, Myung Ho
    CHIRALITY, 2012, 24 (05) : 406 - 411
  • [30] Chiral extraction of amino acid and mandelic acid enantiomers using chiral diphosphine ligands with tunable dihedral angles
    Liu, Xiong
    Ma, Yu
    Liu, Qi
    Wei, Xinyu
    Yang, Jin
    Yu, Lin
    SEPARATION AND PURIFICATION TECHNOLOGY, 2019, 221 : 159 - 165