Hybridization of helical poly(phenylacetylene)s bearing <scp>l</scp>-proline tripeptide pendants into porous silica microspheres as a solvent-tolerable chiral stationary phase for liquid chromatography-Reference-Cited by-同舟云学术

Hybridization of helical poly(phenylacetylene)s bearing l-proline tripeptide pendants into porous silica microspheres as a solvent-tolerable chiral stationary phase for liquid chromatography

Published:2023 Issue:8 Volume:148 Page:1877-1886
ISSN:0003-2654
Container-title:The Analyst
language:en
Short-container-title:Analyst

Author:

Huang Jiahe¹,Zhou Zhengjin¹,Zhang Chunhong¹²^ORCID,Wang Chao¹²,Zhou Yanli¹,Liu Lijia¹²^ORCID,Li Junqing¹,Satoh Toshifumi³^ORCID,Okamoto Yoshio¹⁴^ORCID

Affiliation:

1. Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin, 150001, PR China

2. Yantai Research Institute of Harbin Engineering University, Yantai, 264006, P.R. China

3. Faculty of Engineering, Hokkaido University, Sapporo 060-8628, Japan

4. Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan

Abstract

This paper provided a new hybridization strategy for a poly(phenylacetylene)-based CSP. The HCSP exhibited a good solvent tolerability, and the introduction of CHCl3 into the eluent can improve the chiral resolution performance.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

Electrochemistry,Spectroscopy,Environmental Chemistry,Biochemistry,Analytical Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/AN/D3AN00061C

Reference38 articles.

1. Chiral stationary phases based on lactide derivatives for high-performance liquid chromatography

2. Quaternized chitin used as chiral stationary phase for HPLC and the high enantioseparation of 1,2,3,4-tetrahydro-1-naphthalenamine racemates

3. Chiral separation materials based on derivatives of 6‐amino‐6‐deoxyamylose

4. Chromatographic separation of the interconverting enantiomers of imidazo- and triazole-fused benzodiazepines