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作 者:Yue Li Shu-Ming Kang Ge Shi Yi-Fu Chen Bo-Wen Li Jie Zhang Xin-Hua Wan
机构地区:[1]Beijing National Laboratory for Molecular Sciences,Key Laboratory of Polymer Chemistry and Physics of Ministry of Education,College of Chemistry and Molecular Engineering,Peking University,Beijing,100871,China [2]School of Materials Science and Engineering,Henan Joint International Research Laboratory of Living Polymerizations and Functional Nanomaterials,Henan Key Laboratory of Advanced Nylon Materials and Application,Zhengzhou University,Zhengzhou,450001,China
出 处:《Chinese Journal of Polymer Science》2025年第1期61-69,I0007,共10页高分子科学(英文版)
基 金:supported by the National Natural Science Foundation of China(Nos.52273002 and 52333008);the funding of Boya Postdoctoral Fellowship at Peking University,BMS Junior Fellow Program and the National Funding Program for Postdoctoral Researchers(No.GZC20230031).
摘 要:A series of optically active copolymers with various feed ratios have been synthesized through helix-sense-selective copolymerization catalyzed by[Rh(norbornadiene)Cl]2-triethylamine.This process involves two proline-derived acetylene monomers,(S)-N-(4-chlorophenyl)carbamoyl-2-ethynyl pyrrolidine(MCl)and(S)-N-(tert-butoxycarbonyl)-2-ethynyl pyrrolidine,followed by acidic deprotection and neutralization.These copolymers adopt helical conformations with a preferred handedness,as demonstrated by nuclear magnetic resonance spectroscopy and a series of spectroscopic analyses.The chiroptical activity intensity of copolymer has been found to increase with MCl content.Consequently,the enantioseparation capabilities of copolymers containing 95 mol%,90 mol%,and 85 mol%MCl units have been assessed as chiral stationary phases in high-performance liquid chromatography because of their good chiroptical activities.These chiral stationary phases effectively enantioseparate racemic alcohols,sulfoxides,amides,and metal complexes.Notably,the copolymer with 90 mol%MCl shows superior chiral recognition ability,especially for 1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol(α=1.19)and 4-methylbenzenesulfinamide(α=1.47).Insights from molecular dynamic simulation and autodock analysis indicate that hydrogen bonding andπ-πstacking interactions between the chiral stationary phases and enantiomers play a key role for successful chiral separation.Our contribution not only demonstrates the importance of hydrogen bonding donor and copolymer chiroptical activity of chiral stationary phases for chiral resolution,but will also provide valuable insights for the future development of novel stationary phases.
关 键 词:Helical copolyacetylene Chiral stationary phase High performance liquid chromatography ENANTIOSEPARATION Hydrogen bonding
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