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Journal ArticleDOI

Postsynthetic modification of metal–organic frameworks

Zhenqiang Wang, +1 more
- 21 Apr 2009 - 
- Vol. 38, Iss: 5, pp 1315-1329
TLDR
The rapid increase in reports on PSM demonstrates this methodology will play an increasingly important role in the development of MOFs for the foreseeable future, and in both scope of chemical reactions and range of suitable MOFs.
Abstract
The modification of metal–organic frameworks (MOFs) in a postsynthetic scheme is discussed in this critical review. In this approach, the MOF is assembled and then modified with chemical reagents with preservation of the lattice structure. Recent findings show amide couplings, isocyanate condensations, ‘click’ chemistry, and other reactions are suitable for postsynthetic modification (PSM). In addition, a number of MOFs, from IRMOF-3 to ZIF-90, are amenable to PSM. The generality of PSM, in both scope of chemical reactions and range of suitable MOFs, clearly indicates that the approach is broadly applicable. Indeed, the rapid increase in reports on PSM demonstrates this methodology will play an increasingly important role in the development of MOFs for the foreseeable future (117 references).

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Citations
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Post-Assembly Transformations of Porphyrin-Containing Metal-Organic Framework (MOF) Films Fabricated Via Automated Layer-By-Layer Coordination

TL;DR: In this article, the robustness of layer-by-layer (LbL)-assembled, pillared-paddlewheel-type MOF films toward conversion to new or modified MOFs via solvent-assisted linker exchange (SALE) and post-assembly linker metalation is demonstrated.
Journal ArticleDOI

Site-directed reduction engineering within bimetal-organic frameworks for efficient size-selective catalysis

TL;DR: In this paper, the reducibility of MOF clusters is first revealed via theoretical calculations from the viewpoint of the reduction potential energy (Ereduction), which serves as the basic principle for the site-directed reduction processing of MOFs.
Journal ArticleDOI

Recent advance in porous coordination polymers from the viewpoint of crystalline-state transformation

TL;DR: Recently, research of crystalline-state transformation involving the removal/inclusion of guest molecules in porous coordination polymers (PCPs) was underway as discussed by the authors, which can reveal the intrinsic relevance and interaction between the framework and guest molecules.
Journal ArticleDOI

Synthesis of Isoreticular Zinc(II)‐Phosphonocarboxylate Frameworks and Their Application in the Friedel–Crafts Benzylation Reaction

TL;DR: The catalytic results reveal that ZnPC-2 is an excellent heterogeneous Lewis acid catalyst with a high selectivity towards less bulky para-oriented products.
Journal ArticleDOI

Tuning the Subunits and Topologies in Cluster-Based Cobalt–Organic Frameworks by Varying the Reaction Conditions

TL;DR: In this paper, three tetra-, penta-, and hexanuclear cluster-based cobalt-organic frameworks, [Co2(L)3(HCO2)·MeOH]n (1), [Co5(L),6(OH)2(NO3)2·2H2O]n(2), and [CoL(H CO2)]n (3) [L = (E)-3-(pyridin-3-yl)acrylate], have been successfully synthesized.
References
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Journal ArticleDOI

Functional porous coordination polymers.

TL;DR: The aim is to present the state of the art chemistry and physics of and in the micropores of porous coordination polymers, and the next generation of porous functions based on dynamic crystal transformations caused by guest molecules or physical stimuli.
Journal ArticleDOI

Click Chemistry: Diverse Chemical Function from a Few Good Reactions.

TL;DR: In this paper, a set of powerful, highly reliable, and selective reactions for the rapid synthesis of useful new compounds and combinatorial libraries through heteroatom links (C-X-C), an approach called click chemistry is defined, enabled, and constrained by a handful of nearly perfect "springloaded" reactions.
Journal ArticleDOI

Reticular synthesis and the design of new materials

TL;DR: This work has shown that highly porous frameworks held together by strong metal–oxygen–carbon bonds and with exceptionally large surface area and capacity for gas storage have been prepared and their pore metrics systematically varied and functionalized.
Journal ArticleDOI

Systematic Design of Pore Size and Functionality in Isoreticular MOFs and Their Application in Methane Storage

TL;DR: Metal-organic framework (MOF-5), a prototype of a new class of porous materials and one that is constructed from octahedral Zn-O-C clusters and benzene links, was used to demonstrate that its three-dimensional porous system can be functionalized with the organic groups and can be expanded with the long molecular struts biphenyl, tetrahydropyrene, pyrene, and terphenyl.
Journal ArticleDOI

Design and synthesis of an exceptionally stable and highly porous metal-organic framework

TL;DR: In this article, an organic dicarboxylate linker is used in a reaction that gives supertetrahedron clusters when capped with monocarboxyates.
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