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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
来源:
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
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页数:13
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