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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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Luminescent dimeric polyoxotungstate [Ho(C4H2O6)(α-PW11O39)]216− with magnetism and reversible photochromism

TL;DR: A new organic-inorganic hybrid dimeric phosphotungstate was obtained by the reaction of [P2W19O69(H2O)]14− precursor with Ho3+ ions in the tartaric acid aqueous medium, which was characterized by IR spectrum, X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), energy-dispersive Xray spectrography (EDX), elemental analyses, single-crystal Xray diffraction as discussed by the authors.
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Implications of Crystal Structure on Organotin Carboxylate Photoresists

TL;DR: In this article, a series of five organotin carboxylates of the type [RSn(O)O2CR']6 containing n-butyl ligands and carboxesylates ranging in size from formate to diphenylacetate were synthesized and examined by single crystal X-ray diffraction.
Journal ArticleDOI

Polyanionic clusters embedded in lattice-type hydrogen bonding networks involving in situ bond activation and coupling of organic cations

TL;DR: Two inorganic-organic supramolecular polyoxometalates, (H2chtpy)2[SiW12O40] (1) (chtpy = 1,3,4,6-tetra(4-pyridyl)cyclohexane-1,3-diol) and [Co(Hbztpy), 2]H[AlW12 O40]·3H2O (2) (bztppy =1,2
References
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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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