4.6 Article

Post-modification of covalent organic framework for gas chromatographic separation of isomers

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1673, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.chroma.2022.463085

关键词

Post-modification; Gas chromatography; Isomers; Covalent organic frameworks; Separation

资金

  1. National Natural Science Foundation of China [22176073, 220760 6 6]
  2. Fundamental Research Funds for the Central Universities [JUSRP221002]
  3. Program of Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province

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Separation of isomers is crucial in various fields, but remains challenging due to their similar properties. In this study, a new hydroxyl-functionalized covalent organic framework (COF) was post-modified with [(1-phenylethyl)amino]acetic acid (PEAA) to construct a functionalized COF for the efficient gas chromatographic separation of isomers. The introduced functional groups significantly improved the resolution of isomers.
Separation of isomers is important in diverse areas such as life science, chemical industry, pharmaceutical and environmental science, but still challenging due to their similar physicochemical properties. Devel-opment of new stationary phases is an effective way to improve the performance of chromatography for the separation of isomers. Here, we report the post-modification of a new hydroxyl-functionalized cova-lent organic framework (COF) TzDHNDA with [(1-phenylethyl)amino]acetic acid (PEAA) via esterification reaction to construct PEAA functionalized COF (TzDHNDA-PEAA). The prepared TzDHNDA-PEAA was sta-ble up to 380 & DEG;C and used as stationary phase to make TzDHNDA-PEAA coated capillary column for gas chromatographic separation of isomers. The TzDHNDA-PEAA coated capillary column showed a high col-umn efficiency for n-dodecane (12417 plates m -1, 120 & DEG;C) and high resolution separation of the isomers of fluoroaniline (Rm-/o- = 3.2, Rp-/m- = 2.4), chloroaniline (Rm-/o- = 5.7, Rp-/m- = 1.8), nitrotoluene (Rp-/o-= 2.2, Rm-/p-= 1.7), pinene (R beta-/alpha-= 2.4), ionone (R beta-/alpha-= 4.8) and 1,3-dichloropropene (RE-/Z- = 2.0). The fabricated column offered better separation of chloroaniline isomers than commercial capillary columns InertCap WAX, InertCap 1701 and InertCap 5. The introduced benzene ring, secondary amine and carbonyl groups of PEAA into the COF TzDHNDA significantly improved the resolution of isomers due to the enhanced hydrogen-bonding and pi-pi interactions. This work shows that post-modification strategy is an effective way to prepare novel COFs for chromatographic separation of isomers.(C) 2022 Published by Elsevier B.V.

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