Search results for "Dithiol"

showing 10 items of 143 documents

CCDC 2074278: Experimental Crystal Structure Determination

2021

Related Article: Izar Capel Berdiell, Victor García-López, Mark J. Howard, Miguel Clemente-León, Malcolm A. Halcrow|2021|Dalton Trans.|50|7417|doi:10.1039/D1DT01076J

2-{[5-(12-dithiolan-3-yl)pentanoyl]oxy}ethyl 26-bis(1H-pyrazol-1-yl)pyridine-4-carboxylateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1834563: Experimental Crystal Structure Determination

2018

Related Article: Serhii Krykun, Vincent Croué, Magali Allain, Zoia Voitenko, Juan Aragó, Enrique Ortí, Sébastien Goeb, Marc Sallé|2018|J.Mater.Chem.C|6|13190|doi:10.1039/C8TC04730H

48-bis[45-bis(methylsulfanyl)-2H-13-dithiol-2-ylidene]-48-dihydrobenzo[12-b:45-b']bisthiophene radical cation hexafluorophosphate tetrahydrofuran solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Naphthyridine Derivatives as a Model System for Potential Lithium-Sulfur Energy-Storage Applications

2015

Naphthyridines have been identified as structural elements in sulfurized polyacrylonitrile, which is a common electrode material in lithium–sulfur batteries. Some dibenzonaphthyridine derivatives with a fused dithiolo moiety were prepared as model compounds for battery studies. These heterocyclic systems were prepared via the corresponding diphenyldicarbamide intermediate. Followed by naphthyridione formation, stepwise installation of the dithiolane subunit occurred in a straightforward manner. In the solid state, the heteroaromatic system is completely planar and was thoroughly characterized. Initial battery cycling tests indicated a potential use of such structural motifs in sulfur–lithiu…

Battery (electricity)Organic ChemistryPolyacrylonitrilechemistry.chemical_elementElectrochemistryCombinatorial chemistrySulfurEnergy storageDithiolanechemistry.chemical_compoundchemistryMoietyOrganic chemistryLithiumPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Electrocatalytic Behavior of Tetrathiafulvalene (TTF) and Extended Tetrathiafulvalene (exTTF) [FeFe] Hydrogenase Mimics

2021

TTF- and exTTF-containing [(μ-S2)Fe2(CO)6] complexes have been prepared by the photochemical reaction of TTF or exTTF and [(μ-S2)Fe2(CO)6]. These complexes are able to interact with PAHs. In the absence of air and in acid media an electrocatalytic dihydrogen evolution reaction (HER) occurs, similarly to analogous [(μ-S2)Fe2(CO)6] complexes. However, in the presence of air, the TTF and exTTF organic moieties strongly influence the electrochemistry of these systems. The reported data may be valuable in the design of [FeFe] hydrogenase mimics able to combine the HER properties of the [FeFe] cores with the unique TTF properties

Cultural StudiesHistoryHydrogenaseLiterature and Literary TheoryChemistryFerredoxin HydrogenaseDithiol-Iron(III)-Sulphide ComplexOrganic chemistryQuímicaCombinatorial chemistrychemistry.chemical_compoundQD241-441ComplexTetrathiafulvaleneInorganic chemistryQD146-197ACS Organic & Inorganic Au
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CCDC 162819: Experimental Crystal Structure Determination

2001

Related Article: H.Fleischer, D.Schollmeyer|2001|Acta Crystallogr.,Sect.E:Struct.Rep.Online|57|o330|doi:10.1107/S1600536801004408

Ethanedithiol diacetateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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The effect of tether groups on the spin states of iron(ii)/bis[2,6-di(pyrazol-1-yl)pyridine] complexes

2021

The synthesis of six 2,6-di(pyrazol-1-yl)pyridine derivatives bearing dithiolane or carboxylic acid tether groups is described: [2,6-di(pyrazol-1-yl)pyrid-4-yl]methyl (R)-lipoate (L1), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]ethyl (R)-lipoate (L2), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxy]ethyl (R)-lipoate (L3), N-([2,6-di(pyrazol-1-yl)pyrid-4-ylsulfanyl]-2-aminoethyl (R)-lipoamide (L4), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]acetic acid (L5) and 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]propionic acid (L6). The iron(ii) perchlorate complexes of all the new ligands exhibit gradual thermal spin-crossover (SCO) in the solid state above room temperature, except L4 who…

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundAcetic acidPerchloratechemistrySpin statesCarboxylic acidPyridineFunctional groupRing (chemistry)Medicinal chemistryDithiolaneDalton Transactions
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Preparation and study of silver maleonitriledithiolate complexes

1985

Abstract This paper reports the reaction of Ag2(mnt) and [(NEt4)Ag(mnt)] (mnt2− = maleonitriledithiolate) with PPh3 and 1,2-bis(diphenylphosph

Inorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryDithiolMoleculePhysical and Theoretical ChemistryTriphenylphosphinePhotochemistryPolyhedron
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CCDC 235538: Experimental Crystal Structure Determination

2004

Related Article: J.Vicente, J.-A.Abad, F.S.Hernandez-Mata, B.Rink, P.G.Jones, M.C.R.de Arellano|2004|Organometallics|23|1292|doi:10.1021/om0342964

Iodo-(26-dimethylphenylisocyano)-(25-bis(13-dithiolan-2-yl)-alpha-(26-dimethylphenylimino)benzyl-S)-palladium dichloromethane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Chemically Selective Imaging of Individual Bonds through Scanning Electron Energy-Loss Spectroscopy: Disulfide Bridges Linking Gold Nanoclusters

2020

As proof-of-principle of chemically selective, spatially resolved imaging of individual bonds, we carry out electron energy-loss spectroscopy in a scanning transmission electron microscopy instrument on atomically precise, thiolate-coated gold nanoclusters linked with 5,5'-bis(mercaptomethyl)-2,2'-bipyridine dithiol ligands. The images allow the identification of bridging disulfide bonds (R-S-S-R) between clusters, and X-ray photoelectron spectra support the finding.

Materials scienceScanning electron microscopeDisulfide bondDithiolElectronNanoclusterschemistry.chemical_compoundCrystallographyBipyridinechemistryScanning transmission electron microscopyGeneral Materials SciencePhysical and Theoretical ChemistrySpectroscopyThe Journal of Physical Chemistry Letters
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Group 10 Metal Benzene-1,2-dithiolate Derivatives in the Synthesis of Coordination Polymers Containing Potassium Countercations

2017

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.7b01775

Metal saltsCoordination polymerPotassiumInorganic chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesInorganic ChemistryMetalchemistry.chemical_compoundFirst-principles calculationsGroup (periodic table)Physical and Theoretical ChemistryBenzenechemistry.chemical_classification010405 organic chemistryChemistryPolymerQuímica0104 chemical sciencesCoordination polymersCrystallographyMetal-dithiolene polymersvisual_artvisual_art.visual_art_mediumCoordination compoundsPlatinum
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