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Journal ArticleDOI

Hybrid coordination polymer constructed from β-octamolybdates linked by quinoxaline and its oxidized product benzimidazole coordinated to binuclear copper(I) fragments

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TLDR
The one-dimensional polymer, which consists of beta-[Mo(8)O(26)](4)(-) anions linked by quinoxaline and its oxidized product benzimidazole ligands coordinated to binuclear copper( I) fragments, provides the first demonstration that the isolated copper(I) complex under hydrothermal conditions "captures" the reduction product of original starting organonitrogen ligand to form a copper-beta-octamolybdate complex
Abstract
The one-dimensional polymer, [Cu2(C8H6N2)2(C7H6N2)]2[Mo8O26] (1), which consists of β-[Mo8O26]4- anions linked by quinoxaline and its oxidized product benzimidazole ligands coordinated to binuclear copper(I) fragments, provides the first demonstration that the isolated copper(I) complex under hydrothermal conditions “captures” the reduction product of original starting organonitrogen ligand to form a copper(I)−β-octamolybdate complex.

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Assembly of the Highest Connectivity Wells-Dawson Polyoxometalate Coordination Polymer: the Use of Organic Ligand Flexibility

TL;DR: The structural analyses reveal that the length of flexible bis(triazole) ligands and metal ion coordination geometries have a synergic influence on the structures of this series of Wells-Dawson polyoxoanion-based hybrid compounds.
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Self-Assembly of Polyoxometalate-Based Metal Organic Frameworks Based on Octamolybdates and Copper-Organic Units: from CuII, CuI,II to CuI via Changing Organic Amine

TL;DR: With step by step increasing of the amount of organic amine, the transformation of Cu(II) ions into Cu(I) ones in different degrees in POMs-based metal-organic frameworks (MOFs) for the first time is achieved.
Journal ArticleDOI

Supramolecular isomerism with polythreaded topology based on [Mo8O26]4- isomers.

TL;DR: Two compounds, namely, [Cu(bbi)](2)[Cu(2)(bbi)(2)(delta-Mo(8)O(26))0.5], where bbi is 1,1'-(1,4-butanediyl)bis(imidazole), were synthesized under hydrothermal conditions at different pH values and their crystal structures were determined by X-ray diffraction.
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Formation of a Spiral-Shaped Inorganic−Organic Hybrid Chain, [CuII(2,2‘-bipy)(H2O)2Al(OH)6Mo6O18]nn-: Influence of Intra- and Interchain Supramolecular Interactions

TL;DR: A novel chainlike coordination polymer [Cu(II)(2,2'-bipy)(H(2)O)(2)Al(OH)(6)Mo(6)O(18)](n)()( n)()(-), provides the first example of an extended structure based on an Anderson type of polyanion and a transition metal complex with organic ligand.
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pH-Dependent Assembly of 1D to 3D Octamolybdate Hybrid Materials Based on a New Flexible Bis-[(pyridyl)-benzimidazole] Ligand

TL;DR: In this article, four octamolybdate hybrid materials based on a new flexible multidentate ligand have been synthesized at different pH values under hydrothermal conditions.
References
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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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Organic-Inorganic Hybrid Materials: From "Simple" Coordination Polymers to Organodiamine-Templated Molybdenum Oxides.

TL;DR: A blueprint for the design of oxide materials is provided by nature and members of the ever-expanding class of polymeric coordination complex cations, novel molybdenum oxide substructures, such as the one shown, may be prepared.
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Synthetic Strategies, Structure Patterns, and Emerging Properties in the Chemistry of Modular Porous Solids†

Abstract: The designed construction of extended porous frameworks from soluble molecular building blocks represents one of the most challenging issues facing synthetic chemistry today. Recently, intense research activities directed toward the development of this field have included the assembly of inorganic metal clusters,1 coordination complexes,2 and organic molecules3 of great diversity into extended motifs that are held together either by strong metal-ligand bonding or by weaker bonding forces such as hydrogen-bonding and π-π interactions. Materials that have been produced in this way are referred to as modular since they are assembled from discrete molecules which can be modified to have well-defined function.4 The fact that the integrity of the building blocks is preserved during the synthesis and ultimately translated into the resulting assembled network offers numerous opportunities for designing frameworks with desirable topologies and architectures, thus paving the way for establishing connections between molecular and solid properties. At least three challenges have emerged in this area that must be reckoned with in order for the ideas of rational and designed synthesis of porous materials to become a reality with routine utility. First, it is difficult to control the orientation and stereochemistry of the building blocks in the solid state in order to achieve a given target molecular topology and architecture. Second, in most cases, the products of such assembly reactions are obtained as poorly crystalline or amorphous solids, thus prohibiting their full characterization by single-crystal X-ray diffraction techniques. Third, access to the pores within open structuressan aspect that is so critical to their utility as porous materialssis often prevented by either selfinterpenetration as observed for very open frameworks or strong host-guest interactions that lead to the destruction of the host framework when removal or exchange of guests is attempted. To define and investigate the parameters contributing to the assembly of materials from molecular building blocks, we have established a program aimed at constructing modular porous networks by linking inorganic metal sulfide clusters and organic molecules with transition metal ions. Our work has focused primarily on studying the issues outlined above, and this Account presents our progress toward finding viable and general solutions to these challenges. This is illustrated by some representative examples chosen from the chemistry developed in our research effort for the three building blocks shown in a-c. Their functionality, shape, size, and
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Molecular Manipulation of Microstructures: Biomaterials, Ceramics, and Semiconductors

TL;DR: Three groups of materials-biomaterials, ceramics, and semiconductors-have been selected to illustrate the concept of organic manipulators as used by nature and by synthetic laboratories exploring its potential in materials technology.
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Conducting Layered Organic-inorganic Halides Containing -Oriented Perovskite Sheets

TL;DR: The ability to control perovskite sheet orientation through the choice of organic cation demonstrates the flexibility provided by organic-inorganic perovSKites and adds an important handle for tailoring and understanding lower dimensional transport in layered perovSkites.
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