2019
DOI: 10.1002/chir.23110
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Highly selective recognition of L‐phenylalanine with molecularly imprinted polymers based on imidazolyl amino acid chiral ionic liquid

Abstract: Several amino acid chiral ionic liquids were introduced as functional monomers to prepare molecularly imprinted polymers for specific recognition of Lphenylalanine. Among them, the imprinted polymers L-Phe@MIPs based on[ViImC3][L-Pro] showed the best selective recognition ability for Lphenylalanine. A series of experiments such as dynamic adsorption, static adsorption, and competitive adsorption were conducted to investigate the specific recognition ability and adsorption capacity of the L-Phe@MIPs. It is foun… Show more

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Cited by 12 publications
(3 citation statements)
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References 35 publications
(48 reference statements)
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“…In the following step of the investigation, we aimed to construct the MIP with enhanced binding capacity. It is known from the literature survey that more sophisticated D- and L-phenylalanine imprinted systems, such as MIP conjugates with gold nanoparticles [ 30 ] or MIPs synthesized in the presence of chiral ionic liquids [ 31 ], could affect the binding capacity of the resulted materials, being promising sorbents for separation purposes. However, it should be emphasized that the application of those systems for BNCT could be limited due to biosafety reasons.…”
Section: Resultsmentioning
confidence: 99%
“…In the following step of the investigation, we aimed to construct the MIP with enhanced binding capacity. It is known from the literature survey that more sophisticated D- and L-phenylalanine imprinted systems, such as MIP conjugates with gold nanoparticles [ 30 ] or MIPs synthesized in the presence of chiral ionic liquids [ 31 ], could affect the binding capacity of the resulted materials, being promising sorbents for separation purposes. However, it should be emphasized that the application of those systems for BNCT could be limited due to biosafety reasons.…”
Section: Resultsmentioning
confidence: 99%
“…The synthesis of AACIL was obtained and modified according to the literature 32,33 . The synthesis route is shown in Figure 1.…”
Section: Methodsmentioning
confidence: 99%
“…The synthesis of AACIL was obtained and modified according to the literature. 32,33 The synthesis route is shown in Figure 1. 1. 1-methylimidazole was mixed with 1-bromoethane and stirred back at 70 C for 24 hours, the product was washed with ethyl ether and the unreacted bromoethane was removed to obtain 1-ethyl-3-methylimidazole bromide ([EMIM]Br).…”
Section: Synthesis Of Aacilmentioning
confidence: 99%