High-Precision Size Recognition and Separation in Synthetic 1D Nanochannels

被引:64
作者
Wang, Ping [1 ]
Chen, Xinyi [1 ,2 ,3 ]
Jiang, Qiuhong [1 ]
Addicoat, Matthew [4 ]
Huang, Ning [1 ]
Dalapati, Sasanka [1 ]
Heine, Thomas [5 ]
Huo, Fengwei [2 ,3 ]
Jiang, Donglin [1 ,6 ]
机构
[1] Natl Univ Singapore, Dept Chem, Fac Sci, 3 Sci Dr 3, Singapore 117543, Singapore
[2] Nanjing Tech Univ, Key Lab Flexible Elect, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[3] Nanjing Tech Univ, Inst Adv Mat, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[4] Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, England
[5] Tech Univ Dresden, Dept Theoret Chem, Mommsenstr 13, D-01062 Dresden, Germany
[6] Tianjin Univ, Joint Sch Natl Univ Singapore & Tianjin Univ, Int Campus, Fuzhou 350207, Fujian, Peoples R China
基金
英国工程与自然科学研究理事会;
关键词
covalent organic frameworks; molecular recognition; nanochannels; nanostructures; separation; COVALENT ORGANIC FRAMEWORKS;
D O I
10.1002/anie.201909851
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Covalent organic frameworks (COFs) allow elaborate manufacture of ordered one-dimensional channels in the crystal. We defined a superlattice of COFs by engineering channels with a persistent triangular shape and discrete pore size. We observed a size-recognition regime that is different from the characteristic adsorption of COFs, whereby pore windows and walls were cooperative so that triangular apertures sorted molecules of one-atom difference and notch nanogrooves confined them into single-file molecular chains. The recognition and confinement were accurately described by sensitive spectroscopy and femtosecond dynamic simulations. The resulting COFs enabled instantaneous separation of mixtures at ambient temperature and pressure. This study offers an approach to merge precise recognition, selective transport, and instant separation in synthetic 1D channels.
引用
收藏
页码:15922 / 15927
页数:6
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