期刊文献+

手性共价有机框架合成的研究进展

Research Progress in the Synthesis of Chiral Covalent Organic Frameworks
下载PDF
导出
摘要 共价有机框架(COFs)是一类由有机小分子单体通过共价键连接而成的晶型有机多孔材料,具有良好的化学稳定性、规则的孔道和大的比表面积等优点。而手性共价有机框架(CCOFs)在具备以上优势的同时,还因具有特殊的手性环境,在手性分离、手性识别和不对称催化等领域具有广泛的应用。综述了近年来CCOFs的设计原理及合成方法,阐述了该领域仍存在的挑战和未来的机遇。 Covalent organic frameworks(COFs)are a class of crystalline organic porous materials constructed by organic monomers via covalent bonds,which has the advantages of good chemical stability,regular pores,large specific surface areas and so on.In addition to the above advantages and their special chiral environment chiral covalent organic frameworks(CCOFs)have been widely used in chiral separation,chiral recognition,asymmetric catalysis,et al.The design principles and synthesis methods of CCOFs in recent years are summarized,and the remaining challenges and future opportunities in this field are expounded.
作者 李京晨 赵腾雪 郭彬 郭靖 白宏雨 张晓袁 王立科 LI Jingchen;ZHAO Tengxue;GUO Bin;GUO Jing;BAI Hongyu;ZHANG Xiaoyuan;WANG Like(School of Chemistry and Chemical Engineering,Zhoukou Normal University,Zhoukou 466000,China)
出处 《河南化工》 CAS 2022年第12期8-11,共4页 Henan Chemical Industry
基金 周口师范学院大学生创新创业训练计划资助(S202110478018) 河南省科技攻关计划项目(212102311062)。
关键词 共价有机框架 合成 手性 covalent organic frameworks synthesis chirality
  • 相关文献

参考文献1

二级参考文献90

  • 1Maier MM, Franco P, Lindner W. Separation of enantiomers: needs, challenges, perspectives. J Chromatogr A, 2001, 906:3-33.
  • 2Afonso CAM, Crespo JG. Recent advances in chiral resolution through membrane-based approaches. Angew Chem lnt Ed, 2004, 43: 5293-5295.
  • 3Breuer M, Ditrich K, Habicher T, Hauer B, Kesseler M, Sturmer R, Zelinski T. Industrial methods for the production of optically active intermediates. Angew Chem Int Ed, 2004, 43:788-824.
  • 4Caner H, Groner E, Levy L, Agranat I. Trends in the development of chiral drugs. Drug Discovery Today, 2004, 9:105-110.
  • 5Davankov VA. Enantioselective ligand exchange in modern separa- tion techniques. J ChromatogrA, 2003, 1000:891-915.
  • 6Hara S, Dobashi A. Liquid chromatographic resolution of enantio- mers on normal-phase chiral amide-bonded silica gel: retentions of optically active a-amino acid derivatives on N-acyl homologues of l-valylaminopropylsilanized silica phases. J Chromatogr A, 1979, 186:543-552.
  • 7Hyun MH. Development and application of crown ether-based HPLC chiral stationary phases. Bull Korean Chem Soc, 2005, 26: 1153-1163.
  • 8Steffeck RJ, Zelechonok Y, Gahm KH. Enantioselective separation of racemic secondary amines on a chiral crown ether-based liquid chromatography stationary phase. J Chromatogr A, 2002, 947: 301-305.
  • 9Fanali S. Enantioselective determination by capillary electrophoresis with cyclodextrins as chiral selectors. J Chromatogr A, 2000, 875: 89-122.
  • 10Muderawan IW, Ong TT, Ng SC. Urea bonded cyclodextrin deriva-tives onto silica for chiral HPLC. J Sep Sci, 2006, 29:1849- 1871.

共引文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部