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Journal ArticleDOI

MOFs, MILs and more: concepts, properties and applications for porous coordination networks (PCNs)

Christoph Janiak, +1 more
- 01 Nov 2010 - 
- Vol. 34, Iss: 11, pp 2366-2388
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TLDR
In this paper, a review of metal-organic frameworks (MOFs) and porous coordination polymers (PCPs) with selected examples of their structures, concepts for linkers, syntheses, post-synthesis modifications, metal nanoparticle formations in MOFs, porosity and zeolitic behavior for applications in gas storage for hydrogen, carbon dioxide, methane and applications in conductivity, luminescence and catalysis.
Abstract
This review (over 380 references) summarizes metal–organic frameworks (MOFs), Materials Institute Lavoisier (MILs), iso-reticular metal–organic frameworks (IR-MOFs), porous coordination networks (PCNs), zeolitic metal–organic frameworks (ZMOFs) and porous coordination polymers (PCPs) with selected examples of their structures, concepts for linkers, syntheses, post-synthesis modifications, metal nanoparticle formations in MOFs, porosity and zeolitic behavior for applications in gas storage for hydrogen, carbon dioxide, methane and applications in conductivity, luminescence and catalysis.

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Citations
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Journal ArticleDOI

Carbon dioxide capture-related gas adsorption and separation in metal-organic frameworks

TL;DR: In this article, the authors review the research progress in metal-organic frameworks (MOFs) for CO 2 adsorption, storage, and separations that are directly related to CO 2 capture.
Journal ArticleDOI

Metal Azolate Frameworks: From Crystal Engineering to Functional Materials

TL;DR: A comparison study of 3D Networks Based on Polypyrazolates, Metal 1,2,4-Triazolate Frameworks, and Univalent Coinage-Metal Tetrazolate Framework 1025.
Journal ArticleDOI

Multifunctional metal–organic framework catalysts: synergistic catalysis and tandem reactions

TL;DR: In this review, the applications of MOFs with multiple active sites in synergistic organic catalysis, photocatalysis and tandem reactions are discussed and proposed mechanisms are presented in detail.
References
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Journal ArticleDOI

A Coordination Network That Catalyzes O2-Based Oxidations

TL;DR: IR and powder X-ray diffraction of Tb1 before and after catalysis indicate the catalyst maintains an open framework structure during the catalytic reactions, indicating a catalytically active open-framework pillared layer-type coordination polymer.
Journal ArticleDOI

Mixed-ligand coordination polymers from 1,2-bis(1,2,4-triazol-4-yl)ethane and benzene-1,3,5-tricarboxylate: Trinuclear nickel or zinc secondary building units for three-dimensional networks with crystal-to-crystal transformation upon dehydration

TL;DR: The hydrothermal reaction of M(NO3)2.6H2O with benzene-1,3,5-tricarboxylic acid and 1,2-bis(1,2,4-triazol-4-yl)ethane produced the mixed-ligand coordination polymers (MOFs) that feature trinuclear secondary building units (SBU) within the three-dimensional frameworks.
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Flexible sorption and transformation behavior in a microporous metal-organic framework.

TL;DR: Single-crystal X-ray diffraction experiments show that the ladder structure of the framework is maintained after desolvation of the material, resulting in the production of a porous solid stable to 215(4) degrees C.
Journal ArticleDOI

A New Type of Two-Dimensional Metal Coordination Systems: Hydrothermal Synthesis and Properties of the First Oxalate−bpy Mixed-Ligand Framework [M(ox)(bpy)] (M = Fe(II), Co(II), Ni(II), Zn(II); ox = C2O42-; bpy = 4,4‘-bipyridine)

TL;DR: In this article, a new family of two-dimensional metal coordination polymers with the general formula [M(ox)(bpy) have been designed and synthesized via hydrothermal routes.
Journal ArticleDOI

Loading of MOF-5 with Cu and ZnO Nanoparticles by Gas-Phase Infiltration with Organometallic Precursors : Properties of Cu/ZnO@MOF-5 as Catalyst for Methanol Synthesis

TL;DR: The loading of [Zn4O(bdc)3] (MOF-5; bdc = 1,4-benzenedicarbocylate) with nanocrystalline Cu and ZnO species was achieved in a two-step process as discussed by the authors.
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