Synthesis of a novel chiral DA-TD covalent organic framework for open-tubular capillary electrochromatography enantioseparation-Reference-Cited by-同舟云学术

Synthesis of a novel chiral DA-TD covalent organic framework for open-tubular capillary electrochromatography enantioseparation

Published:2022 Issue:3 Volume:58 Page:403-406
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wang Guoxiu¹²,Lv Wenjuan¹²,Pan Congjie¹²^ORCID,Chen Hongli¹²^ORCID,Chen Xingguo¹²³^ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu 730000, China

2. Department of Chemistry, Lanzhou University, Lanzhou 730000, China

3. Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, Lanzhou University, Lanzhou, Gansu 730000, China

Abstract

A novel chiral covalent organic framework (CCOF), DA-TD COF, with good chemical/thermal stability was synthesized and acts as a chiral stationary phase for open-tubular capillary electrochromatography enantioseparation.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CC/D1CC06420G

Reference21 articles.

1. Enantioseparation and molecular modeling study of eight psychoactive drugs on a coated polysaccharide‐based chiral stationary phase

2. Enantiomers separation by capillary electrochromatography using polysaccharide-based stationary phases

3. Enantioseparation of N‐ acetyl‐glutamine enantiomers by LC–MS/MS and its application to a plasma protein binding study

4. Pico-HPLC system integrating an equal inner diameter femtopipette into a 900 nm I.D. porous layer open tubular column

5. Engineering a homochiral metal–organic framework based on an amino acid for enantioselective separation

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