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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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Journal ArticleDOI

Biopolymer@Metal-Organic Framework Hybrid Materials: A Critical Survey

TL;DR: In this article, a review article spotlights the fashionable trend in bridging the field of MOF-based materials through the use of bio-based precursors (mainly biopolymers) and discusses how the holistic association of the MOF crystals and the biopolymer matrices resulted in promising materials with prominent properties.
Journal ArticleDOI

Enhancing CO2 adsorption of a Zn-phosphonocarboxylate framework by pore space partitions.

TL;DR: Using structure-directing agents, pore space partitions of a Zn-phosphonocarboxylate framework have been achieved and selective adsorption of CO(2) over N( 2) has been greatly improved.
Journal ArticleDOI

Selective Adsorption Properties of Cationic Metal–Organic Frameworks Based on Imidazolic Linker

TL;DR: In this article, the imidazolium salt linker H2ImidCl was prepared in five steps and converted with zinc and copper nitrate, respectively, to give two topologically different cationic frameworks.
Journal ArticleDOI

Recent progress on synthesis of ZIF-67-based materials and their application to heterogeneous catalysis

TL;DR: In this paper, the authors summarized the latest strategies of synthesizing ZIF-67-based materials by exploring the prominent examples and shed some light on the large-scale industrial production of Zif-67based materials and their applications.
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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