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  • 教授
  • 博士生导师
  • 硕士生导师
  • 教师拼音名称:Zhu Chengfeng
  • 电子邮箱:
  • 入职时间:2013-10-30
  • 所在单位:化学与化学学院
  • 学历:博士研究生毕业
  • 联系方式:18256961217
  • 学位:博士学位
  • 在职信息:在职
  • 毕业院校:上海交通大学
  • 学科:应用化学
    化学其他专业
论文成果
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Homochiral Dodecanuclear Lanthanide “Cage in Cage” for Enantioselective Separation
  • DOI码:10.1021/jacs.1c03652
  • 发表刊物:Journal of the American Chemical Society
  • 摘要:It is extremely difficult to anticipate the structure and the stereochemistry of a complex, particularly when the ligand is flexible and the metal node adopts diverse coordination numbers. When trivalent lanthanides (LnIII) and enantiopure amino acid ligands are utilized as building blocks, self-assembly sometimes yields rare chiral polynuclear structures. In this study, an enantiopure carboxyl-functionalized amino acid-based ligand with C3 symmetry reacts with lanthanum cations to give a homochiral porous coordination cage, (Δ/Λ)12-PCC-57.The dodecanuclear lanthanide cage has an unprecedented octahedral “cagein-cage” framework. During the self-assembly, the chirality is transferred from the enantiopure ligand and fixed by the binuclear lanthanide cluster to give 12 metal centers that have either Δ or Λ homochiral stereochemistry. The cage exhibits excellent enantioselective separation of racemic alcohols, 2,3-dihydroquinazolinones, and multiple commercially available drugs. This finding exhibits a rare example of a multinuclear lanthanide complex with a dual-walled topology and homochirality. The highly ordered self-assembly and self-sorting of flexible amino acids and lanthanides shed light on the chiral transformation between different complicated artificial systems that mimic natural enzymes.
  • 论文类型:期刊论文
  • 通讯作者:Zhu Chengfeng* et al.,
  • 学科门类:理学
  • 文献类型:J
  • 卷号:143
  • 期号:32
  • 页面范围:12560-12566
  • 是否译文:
  • 发表时间:2021-08-03
  • 收录刊物:SCI
  • 发布期刊链接:https://pubs.acs.org/doi/10.1021/jacs.1c03652
  • 附件: homochiral-dodecanuclear-lanthanide-cage-in-cage-for-enantioselective-separation.pdf