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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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Electron transfer in the confined environments of metal-organic coordination supramolecular systems.

TL;DR: An overview of significant progress in the photophysical and catalytic applications of supramolecular host-guest systems with electron-transfer processes in confined environments and special emphasis is placed on the action modes and regulatory factors that affect electron transfer between different components to produce enhanced photophysical or redox catalytic performance.
Journal ArticleDOI

Polyoxometalates paneling through {Mo2O2S2} coordination: cation-directed conformations and chemistry of a supramolecular hexameric scaffold.

TL;DR: Density functional methodology (DFT) has been applied to compute the geometries and energies of dimer (3), tetramer (2), and hexamer (1) based on {AsW(9)O(33)} (POM) and {Mo(2)O (2)S(2)} (L) units.
Journal ArticleDOI

Time‐Resolved Assembly of Cluster‐in‐Cluster {Ag12}‐in‐{W76} Polyoxometalates under Supramolecular Control

TL;DR: Time-resolved supramolecular assembly of a series of nanoscale polyoxometalate clusters of the form of [H(10+m)Ag18Cl(Te3W38O134)2]n is reported, demonstrating the crucial role that TeO3(2-), Cl(-), and Ag(+) play in the self-assembly of compounds 1-3.
Journal ArticleDOI

Unprecedented high-nuclear transition-metal-cluster-substituted heteropolyoxoniobates: synthesis by {V8 } ring insertion into the POM matrix and antitumor activities.

TL;DR: Nickel and zinc cations have been introduced into HPNs for the first time, which might promise a more diverse set of structures in this family of heteropolyoxoniobates.
Journal ArticleDOI

Supramolecular architectures assembled from amphiphilic hybrid polyoxometalates

TL;DR: The current progresses are summarized and some perspectives are provided, from colloidal chemists' point of view, on the self-assembly of the amphiphilic POM-organic hybrids in solution and at interfaces, as well as the related consequent novel features such as enhanced fluorescent properties.
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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