A Redox-Active Bistable Molecular Switch Mounted inside a Metal-Organic Framework

被引:119
作者
Chen, Qishui [1 ]
Sun, Junling [1 ]
Li, Peng [1 ]
Hod, Idan [1 ]
Moghadam, Peyman Z. [2 ,4 ]
Kean, Zachary S. [1 ]
Snurr, Randall Q. [2 ]
Hupp, Joseph T. [1 ]
Farha, Omar K. [1 ,3 ]
Stoddart, J. Fraser [1 ]
机构
[1] Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[3] King Abdulaziz Univ, Fac Sci, Dept Chem, Jeddah 21589, Saudi Arabia
[4] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge, England
关键词
MECHANICALLY INTERLOCKED MOLECULES; DONOR-ACCEPTOR; THIN-FILM; MACHINES; DYNAMICS; SHUTTLE; MOTORS; ROTAXANES; NU-1000; ETHERS;
D O I
10.1021/jacs.6b09880
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe the incorporation of a bistable mechanically interlocked molecule (MIM) into a robust Zr-based metal organic framework (MOF), NU-1000, by employing a post-synthetic functionalization protocol On average, close to two bistable [2]catenanes can be incorporated per repeating unit of the hexagonal channels of NU-1000. The reversible redox-switching of the bistable [2]catenanes is retained inside the MOF, as evidenced by solid-state UV-vis-NIR reflectance spectroscopy and cyclic voltammetry. This research demonstrates that bistable MIMs are capable of exhibiting robust dynamics inside the nanopores of a MOF;
引用
收藏
页码:14242 / 14245
页数:4
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