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Uncovering Structural Opportunities for Zirconium Metal–Organic Frameworks via Linker Desymmetrization
Author(s) -
Wang Yutong,
Feng Liang,
Zhang Kai,
Wang KunYu,
Fan Weidong,
Wang Xiaokang,
Guo Bingbing,
Dai Fangna,
Zhang Liangliang,
Sun Daofeng,
Zhou HongCai
Publication year - 2019
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.201901855
Subject(s) - linker , bent molecular geometry , desymmetrization , topology (electrical circuits) , cluster (spacecraft) , materials science , joins , chemistry , crystallography , combinatorial chemistry , computer science , organic chemistry , catalysis , combinatorics , mathematics , programming language , enantioselective synthesis , operating system
The discovery of metal–organic frameworks (MOFs) mimicking inorganic minerals with intricate topologies requires elaborate linker design guidelines. Herein, the concept of linker desymmetrization into the design of tetratopic linker based Zr‐MOFs is applied. A series of bent tetratopic linkers with various substituents are utilized to construct Zr‐MOFs with distinct cluster connectivities and topologies. For example, the assembly between a bent linker L‐SO 2 with C 2v symmetry and an 8‐connected Zr 6 cluster leads to the formation of an scu topology, while another flu topology can be obtained by the combination of a novel 8‐connected Zr 6 cluster and a bent linker L‐O with C 1 symmetry. Further utilization of restricted bent linker [(L‐(CH 3 ) 6 )] gives rise to a fascinating (4, 6)‐c cor net, originated from the corundum lattice, with an unprecedented 6‐c Zr 6 cluster. In addition, the removal of toxic selenite ions in aqueous solution is performed by PCN‐903‐(CH 3 ) 6 which exhibits rapid and efficient detoxification. This work uncovers new structural opportunities for Zr‐MOFs via linker desymmetrization and provides novel design strategies for the discovery of sophisticated topologies for practical applications.

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