RESUMEN
Sequence-defined nucleic acids and proteins with internal monomer sequences and arrangement are vital components in the living world, as a result of billions of years of molecular evolution. These natural hierarchical systems have inspired researchers to develop artificial hierarchical materials that can mimic similar functions such as replication, recognition, and information storage. In this Outlook, we describe the conceptual introduction of hierarchy into the design of metal-organic framework (MOF) materials. Starting with a history and background of hierarchical MOF synthesis and applications, we discuss further mesoscopic assembly strategies of MOF crystallites into hierarchical primary, secondary, tertiary, and quaternary architectures. This is followed by a highlight of the utilization of modular total synthesis for crafting MOFs with hierarchical compositions. The multiscale control over hierarchical MOF architecture formation can be rationally achieved by designing stepwise synthetic routes based on the knowledge from various fields including coordination chemistry, organic chemistry, reticular chemistry, and nanoscience. Altogether, this outlook is expected to shed light on these essential but embryonic materials and might offer inspiration for the development of the next generation of smart MOF materials with controllable heterogeneity and tailorable architectures.
RESUMEN
Sophisticated chemical processes widely observed in biological cells require precise apportionment regulation of building units, which inspires researchers to develop tailorable architectures with controllable heterogeneity for replication, recognition and information storage. However, it remains a substantial challenge to endow multivariate materials with internal sequences and controllable apportionments. Herein, we introduce a novel strategy to manipulate the apportionment of functional groups in multivariate metal-organic frameworks (MTV-MOFs) by preincorporating interlocked linkers into framework materials. As a proof of concept, the imprinted apportionment of functional groups within ZIF-8 was achieved by exchanging imine-based linker templates with original linkers initially. The removal of linker fragments by hydrolysis can be achieved via postsynthetic labilization, leading to the formation of architectures with controlled heterogeneity. The distributions of functional groups in the resulting imprinted MOFs can be tuned by judicious control of the interlocked chain length, which was further analyzed by computational methods. This work provides synthetic tools for precise control of pore environment and functionality sequences inside multicomponent materials.
RESUMEN
The production of two-dimensional (2D) ultrathin metal-organic framework (MOF) nanosheets with functionalized surfaces is significant for extending their applications. To date, no protocol has been developed yet to solve this problem. Herein, we report a facile, mild, and efficient method to produce 2D monolayer MOF nanosheets with hydrophobic surfaces from layer-pillared 3D MOFs. This approach is based on the replacement of weaker coordinating pillar ligands with stronger coordinating capping ligands with the assistance of a high concentration gradient of the latter. Utilizing this method, the replacement of the 4,4'-bipyridine (bpy) pillars in two cadmium-based layer-pillared MOFs with alkylpyridine derivatives has been achieved, producing 2D MOF nanosheets with monolayer thickness and double-sided hydrophobic surfaces. The resulting hydrophobic 2D MOF nanosheets exhibit good performance for the separation of oil and water.
