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Journal ArticleDOI

Hybrid Organic−Inorganic Polyoxometalate Compounds: From Structural Diversity to Applications

TLDR
Polyoxometalates (POMs) are discrete anionic metaloxygen clusters which can be regarded as soluble oxide fragments which play a great role in various areas ranging from catalysis, medicine, electrochemistry, photochromism,5 to magnetism.
Abstract
Polyoxometalates (POMs) are discrete anionic metaloxygen clusters which can be regarded as soluble oxide fragments. They exhibit a great diversity of sizes, nuclearities, and shapes. They are built from the connection of {MOx} polyhedra, M being a d-block element in high oxidation state, usually VIV,V, MoVI, or WVI.1 While these species have been known for almost two centuries, they still attract much interest partly based on their large domains of applications. They play a great role in various areas ranging from catalysis,2 medicine,3 electrochemistry,4 photochromism,5 to magnetism.6 This palette of applications is intrinsically due to the combination of their added value properties (redox properties, large sizes, high negative charges, nucleophilicity...). Parallel to this domain, the organic-inorganic hybrids area has followed a similar expansion during the last 10 years. The concept of organic-inorganic hybrid materials * To whom correspondence should be addressed. E-mail: dolbecq@ chimie.uvsq.fr. Chem. Rev. 2010, 110, 6009–6048 6009

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{Mn14W48} aggregate: the perspective of isopolyanions as ligands

TL;DR: The assembly of a tetradeca-manganese magnetic cluster, containing two high spin Mn(7) cores and supported exclusively by isopolytungstate ligands, demonstrates the promising perspective of using "defect" isopolyanions as ligands/synthons to construct large aggregated structures and model the surface deposition of molecular magnets.
Journal ArticleDOI

Structure and bifunctional electrocatalytic activity of a novel 3D framework based on dimeric monocopper-substituted polyoxoanions as ten-connected linkages

TL;DR: In this paper, a unique hybrid compound with dimeric monocopper-substituted Keggin polyoxoanions as ten-connected linkages, [Cu5(en)9][(PW11CuO39)2]·18H2O (1) (en = ethylenediamine), has been synthesized and characterized by elemental analysis, IR, TG analysis, powder X-ray diffraction and single-crystal X-Ray diffraction.
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Polyoxometalate anion–π interaction-directed assembly of a three-dimensional hydrogen-bonded supramolecular framework with nanoscale porosity

TL;DR: In this article, a rare three-dimensional hydrogen-bonded supramolecular framework composed of octahedral [Cr(H3O)3(H2O)6+ ions and linear π-electron-deficient N,N′-di(4-pyridyl)-1,4,5,8-naphthalenediimide (DPNDI) tectons was formed in the presence of electron-rich polyoxometalates by less common noncovalent anion-π interactions, indicating that poly
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Coassembly of Mixed Weakley-Type Polyoxometalates to Novel Nanoflowers with Tunable Fluorescence for the Detection of Toluene

TL;DR: The results provide a new avenue to the facile construction of fluorescent composites and demonstrate that the POM complexes can be further used in supramolecular chemistry and nanomaterials.
References
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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.
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Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides.

TL;DR: A novel regiospecific copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes to azides on solid-phase is reported, and the X-ray structure of 2-azido-2-methylpropanoic acid has been solved, to yield structural information on the 1, 3-dipoles entering the reaction.
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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.
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