Search results for "tetrathiafulvalene"

showing 10 items of 159 documents

Quinonoid π-extended tetrathiafulvalenes (TTFs)

2001

Publisher Summary Tetrathiafulvalene (TTF) is a fascinating planar πelectron-donor molecule with a broad range of potential applications. TTF and its derivatives play an important role in the field of organic conductors forming charge-transfer (CT) complexes and radical cation salts (Bechgaard salts) with a huge variety of electron-acceptor molecules and anions in the search for electrically conducting and superconducting materials. The chapter focuses on highly π-extended electron donors with p-quinodimethane structures as interesting precursors of materials with non-conventional properties. The first dimeric examples of π-extended TTF derivatives connected through an oxygen atom are also …

chemistry.chemical_classificationchemistry.chemical_compoundCrystallographyFullerenechemistryRadical ionCovalent bondStereochemistryMoietyMoleculeConjugated systemElectron acceptorTetrathiafulvalene
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Metallic Conductivity in a Polyoxovanadate Radical Salt of Bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF): Synthesis, Structure, and Physical Chara…

2004

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryMechanics of MaterialsMechanical EngineeringMetallic conductivityInorganic chemistryPolymer chemistrySalt (chemistry)General Materials ScienceTetrathiafulvaleneCharacterization (materials science)Advanced Materials
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The first radical salt of the polyoxometalate cluster [P2W18O62]6⊖with bis(ethylenedithio)tetrathiafulvalene (ET): ET11[P2W18O62] · 3H2O

1996

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryMechanics of MaterialsMechanical EngineeringOrganometallic polymerPolyoxometalateCluster (physics)Organic chemistrySalt (chemistry)General Materials ScienceTetrathiafulvaleneAdvanced Materials
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Discrete supramolecular donor-acceptor complexes

2009

The renewed interest in noncovalently associating electroactive molecules arises in part from the quest for new organic materials that convert solar energy into electrical/ chemical equivalents. In this context, the formation of charge-separated states is a key prerequisite. Charge-transfer events triggered by light have been studied in supramolecular donor–acceptor systems based on hydrogen bonds and coordinative metal bonds. Although many of the most widely utilized electroactive fragments feature large pconjugated surfaces, to date the use of p–p aromatic interactions has mainly been limited to the construction of semi-infinite ensembles of chromophores either to achieve charge transport…

chemistry.chemical_compoundChemistryHydrogen bondComputational chemistryTweezersSupramolecular chemistryMoleculePi interactionContext (language use)General ChemistryChromophoreCatalysisTetrathiafulvalene
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Concave Tetrathiafulvalene-Type Donors as Supramolecular Partners for Fullerenes

2007

The cap fits! A new class of concave π-extended tetrathiafulvalene (TTF) derivatives, truxene-TTFs, were prepared and characterized, and their self-assembly with fullerenes was investigated (see picture). Truxene-TTFs represent the first example of TTF-related electron donors that serve, without chemical modification, as monotopic receptors for fullerenes in solution. (Chemical Equation Presented). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

chemistry.chemical_compoundCrystallographyFullerenechemistryStereochemistrySupramolecular chemistryChemical modificationGeneral ChemistrySelf-assemblyGeneral MedicineChemical equationCatalysisTetrathiafulvaleneAngewandte Chemie
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Investigation of Charge-Transfer Interactions Induced by Encapsulating Fullerene in a Mesoporous Tetrathiafulvalene-Based Metal-Organic Framework

2019

<p>The design of Metal-Organic Frameworks (MOFs) incorporating electroactive guest molecules in the pores has become a subject of great interest in order to install additional electrical functionalities within the framework while maintaining porosity. In this direction, understanding the charge-transfer (CT) process between the framework and the guest molecules is crucial towards the design of new electroactive MOFs. Herein, we present the encapsulation of fullerenes (C<sub>60</sub>) in a mesoporous tetrathiafulvalene(TTF)-based MOF. The CT process between the electron-acceptor C<sub>60 </sub>guest and the electron-donor TTF ligand is studied in detail by means…

chemistry.chemical_compoundMaterials scienceFullerenechemistryMoleculeMetal-organic frameworkNanotechnologySorptionDensity functional theoryMesoporous materialPorosityTetrathiafulvalene
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Polyoxometalate-Based Molecular Materials.

1998

Molecule-based materials with active physical properties, in particular electrical, magnetic, and optical, are a focus of contemporary materials chemistry research. Certainly, one reason for this interest has been the realization that these materials can exhibit cooperative properties typically associated with the inorganic network solids, as for example metallic conduction or even superconductivity,1 ferromagnetism,2 and nonlinear optical properties.3 With respect to the electrical properties, many important achievements were obtained in the 1970s with the discovery of the first molecule-based metal in 1972,4 namely the π-electron donor-acceptor complex [TTF][TCNQ] (TTF ) tetrathiafulvalen…

chemistry.chemical_compoundSolid-state chemistrychemistryFerromagnetismChemical physicsPolyoxometalateNetwork covalent bondingMoleculeGeneral ChemistryTetracyanoethyleneHybrid materialTetrathiafulvaleneChemical reviews
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Crystal structure of bis(ethylenedithio)tetrathiafulvalenium μ2-acetato-bis[tribromidorhenate(III)] 1,1,2-trichloroethane hemisolvate

2016

The crystal structure of a binuclear mono­carboxyl­ato dirhenium(III) complex with a fulvalene derivative is reported. This compound represents a radical cation salt containing a cluster unit with rhenium–rhenium quadruple bond.

crystal structureStereochemistrybis­(ethyl­enedi­thio)­tetra­thia­fulvaleneStackingThio-Crystal structurerhenium010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesResearch CommunicationsCrystalquadruple metal–metal bondbis(ethylenedithio)tetrathiafulvaleneGeneral Materials Scienceradical cation saltCrystallographybiologyHydrogen bondChemistryLigandGeneral ChemistryCondensed Matter Physicsbiology.organism_classification0104 chemical sciencesCrystallographyRadical ionQD901-999TetraActa Crystallographica Section E: Crystallographic Communications
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Magnetic transition metal complexes of tetrathiafulvalene (TTF) derivatives

1997

We have prepared and characterized the transition metal complexes of two different TTF derivatives. We have oxidized the different complexes with electrooxidation and chemical oxidation techniques and the results are discussed. The magnetic properties of the complexes have been studied. TTF-carboxylate chelates are not stable enough, but thioether-TTF shows promising charge transfer salts.

endocrine systemMagnetic measurementsTtf derivativesChemistryMechanical EngineeringInorganic chemistryMetals and AlloysCharge (physics)respiratory systemCondensed Matter PhysicsMagnetic susceptibilityElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundTransition metalMechanics of MaterialslawMaterials ChemistryPhysical chemistryChelationElectron paramagnetic resonanceTetrathiafulvalene
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Self-Assembled Molecular Rafts at Liquid|Liquid Interfaces for Four-Electron Oxygen Reduction

2011

The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetramethylpyridinium porphyrin (CoTMPyP(4+)) and cobalt tetrasulphonatophenyl porphyrin (CoTPPS(4-)), at the interface with an organic solvent to form molecular "rafts", provides an excellent catalyst to perform the interfacial four-electron reduction of oxygen by lipophilic electron donors such as tetrathiafulvalene (TTF). The catalytic activity and selectivity of the self-assembled catalyst toward the four-electron pathway was found to be as good as that of the Pacman type cofacial cobalt porphyrins. The assembly has been characterized by UV-visible spectroscopy, Surface Second Harmonic Generation, and Scanning …

inorganic chemicals2Nd-Harmonic Generationchemistry.chemical_elementPhotochemistryBiochemistryOxygenCatalysisCatalysischemistry.chemical_compoundWater-Soluble PorphyrinsColloid and Surface ChemistryCobalt Porphyrinsheterocyclic compoundsLiquid/Liquid Interface2Nd DerivativesEnergyDioxygenPolarizable Continuum ModelGeneral ChemistryPorphyrinRadical CationchemistryRadical ionSurface second harmonic generationDensity functional theoryImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
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