Polydopamine-assisted immobilization of a zinc(II)-derived metal-organic cage as a stationary phase for open-tubular capillary electrochromatography

A capillary column was modified with a soluble zinc(II)-derived metal-organic cage (MOC) [Zn 2 L] as the stationary phase to obtain a new coating layer for use in open-tubular capillary electrochromatography. The inner surface of the capillary was first coated with a layer of polydopamine. Then, a s...

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Veröffentlicht in:Mikrochimica acta (1966) 2019-07, Vol.186 (7), p.449-449, Article 449
Hauptverfasser: Li, Zhentao, Mao, Zhenkun, Chen, Zilin
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Mao, Zhenkun
Chen, Zilin
description A capillary column was modified with a soluble zinc(II)-derived metal-organic cage (MOC) [Zn 2 L] as the stationary phase to obtain a new coating layer for use in open-tubular capillary electrochromatography. The inner surface of the capillary was first coated with a layer of polydopamine. Then, a solution of the MOC in dichloromethane was introduced into the capillary upon which it is bonded both covalently and non-covalently. The resulting coating layer on the capillary was characterized by scanning electron microscopy and Fourier transform infrared spectroscopy. The results demonstrated the successful formation of the [Zn 2 L] modified open-tubular column. The column showed good separation performance towards neutral compounds (such as methylbenzene, ethylbenzene, n-propylbenzene and n-butylbenzene), acidic drugs (such as ibuprofen, ketoprofen, flurbiprofen and diclofenac sodium), food additives (such as parabens, vanillin and related phenolic compounds) and small biomolecules (such as nucleosides and nucleotide bases) by π-interaction and hydrophobic interaction. It also exhibited good precision, the relative standard deviations of the retention time for intra-day, inter-day runs and column-to-column being
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The inner surface of the capillary was first coated with a layer of polydopamine. Then, a solution of the MOC in dichloromethane was introduced into the capillary upon which it is bonded both covalently and non-covalently. The resulting coating layer on the capillary was characterized by scanning electron microscopy and Fourier transform infrared spectroscopy. The results demonstrated the successful formation of the [Zn 2 L] modified open-tubular column. The column showed good separation performance towards neutral compounds (such as methylbenzene, ethylbenzene, n-propylbenzene and n-butylbenzene), acidic drugs (such as ibuprofen, ketoprofen, flurbiprofen and diclofenac sodium), food additives (such as parabens, vanillin and related phenolic compounds) and small biomolecules (such as nucleosides and nucleotide bases) by π-interaction and hydrophobic interaction. It also exhibited good precision, the relative standard deviations of the retention time for intra-day, inter-day runs and column-to-column being &lt;1.6%, 2.8%, and 4.0%, respectively. 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It also exhibited good precision, the relative standard deviations of the retention time for intra-day, inter-day runs and column-to-column being &lt;1.6%, 2.8%, and 4.0%, respectively. 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It also exhibited good precision, the relative standard deviations of the retention time for intra-day, inter-day runs and column-to-column being &lt;1.6%, 2.8%, and 4.0%, respectively. Graphical abstract Schematic presentation of the open-tubular column modified with zinc(II)-derived metal-organic cage by polydopamine-assisted strategy onto the inner wall of capillary for electrochromatographic separations.</abstract><cop>Vienna</cop><pub>Springer Vienna</pub><pmid>31197494</pmid><doi>10.1007/s00604-019-3576-5</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9824-9987</orcidid></addata></record>
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subjects Analytical Chemistry
Characterization and Evaluation of Materials
Chemistry
Chemistry and Materials Science
Chromatography
Diclofenac
Food additives
Infrared spectroscopy
Microengineering
Nanochemistry
Nanotechnology
Original Paper
title Polydopamine-assisted immobilization of a zinc(II)-derived metal-organic cage as a stationary phase for open-tubular capillary electrochromatography
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