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Guo, Bingbing

Publications and source records attributed to Guo, Bingbing.

Uncovering Structural Opportunities for Zirconium Metal–Organic Frameworks via Linker Desymmetrization

Abstract 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.

Chemistry↗

Molecular Pivot-Hinge Installation to Evolve Topology in Rare-Earth Metal–Organic Frameworks

Linker desymmetrization has been witnessed as a powerful design strategy for the discovery of highly connected metal–organic frameworks (MOFs) with unprecedented topologies. Herein, we introduce molecular pivot-hinge installation as a linker desymmetrization strategy to evolve the topology of highly connected rare-earth (RE) MOFs, where a pivot group is placed in the center of a linker similar to a hinge. By tuning the composition of pivot groups and steric hindrances of the substituents on various linker rotamers, MOFs with various topologies can be obtained. The combination of L-SO 2 with C 2v symmetry and 12-connected RE9 clusters leads to the formation of a fascinating (4,12)-c dfs new topology. Interestingly, when replacing L-SO 2 with a tetrahedra linker L-O, the stacking behaviors of RE-organic layers switch from an eclipsed mode to a staggered stacking mode, leading to the discovery of an intriguing hjz topology. Additionally, the combination of the RE cluster and a linker [(L-(CH 3 ) 6 )] with more bulky groups gives rise to a flu topology with a new 8-c inorganic cluster. The diversity of these RE-MOFs was further enhanced through post-synthetic installation of linkers with various functional groups. Functionalization of each linker with acidic and basic units in the mesoporous RE-based PCN-90-SO 2 allows for efficient cascade catalytic transformation within the functionalized channels.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗