Search results for "bonding"

showing 10 items of 996 documents

Structure and vibrational features of the protic ionic liquid 1,8-diazabicyclo[5.4.0]-undec-7-ene-8-ium bis(trifluoromethanesulfonyl)amide, [DBUH][TF…

2022

Abstract The Protic Ionic Liquid (PIL) formed by neutralization of the super-strong base 1,7-diazabicyclo[5.4.0]undec-7-ene (DBU) with the super-strong acid bis(trifluoromethanesulfonyl)-imide (TFSI), indicated as [DBUH][TFSI], has been investigated. Its chemical physical properties and structural features have been explored using a synergy of experimental and computational tools. Molecular Dynamics-rationalised X-ray diffraction patterns highlight the major role played by hydrogen bonding (HB) in affecting morphology in this PIL. A comparison between HB features in this and in related PILs has been presented, on the base of far-IR experiments and DFT analysis. Indications of a weaker HB in…

Hydrogen bondingMaterials scienceProtic Ionic LiquidBase (chemistry)DFT calculationMolecular Dynamics010402 general chemistry01 natural scienceschemistry.chemical_compoundDFT calculation; Far-ir spectroscopy; Hydrogen bonding; Molecular Dynamics; Protic Ionic Liquid; X-ray scatteringPhase (matter)Materials ChemistryFar-ir spectroscopyPhysical and Theoretical ChemistryConformational isomerismSpectroscopychemistry.chemical_classification010405 organic chemistryHydrogen bondX-ray scatteringCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallography18-Diazabicyclo[5.4.0]undec-7-enechemistryAbsorption bandIonic liquidDispersion (chemistry)Journal of Molecular Liquids
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Crystal structure of the tetraaquabis(thiocyanato-kappa N)cobalt(II)-caffeine-water (1/2/4) co-crystal

2017

In the structure of the title compound, [Co(NCS)2(H2O)4]·2C8H10N4O2·4H2O, the cobalt metal lies on an inversion centre and is coordinated in a slightly distorted octa­hedral geometry. In the crystal, the complex mol­ecules inter­act with the caffeine mol­ecules through O—H⋯N, O—H⋯O, C–H⋯S hydrogen bonds and π–π inter­actions.

Hydrogen bondingSingle-crystal X-ray diffraction analysischemistry.chemical_elementThio-Crystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesResearch CommunicationsCrystallcsh:ChemistryCaffeineGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistrybiologyHydrogen bondCrystal structureGeneral ChemistryCondensed Matter Physicsbiology.organism_classification3. Good health0104 chemical sciencesCrystallographyOxygen atomchemistrylcsh:QD1-999TetraCobalt
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Hydrogen bonding and proton transfer involving the trihydride complexes Cp*M(dppe)H 3 (M = Mo, W) and fluorinated alcohols: the competitive role of t…

2003

International audience; The protonation of complexes Cp*M(dppe)H3 (dppe is ethylenebis(diphenylphosphine), M = Mo (1), W (2)) by a variety of fluorinated alcohols of different acid strength (FCH2CH2OH, CF3CH2OH, (CF3)2CHOH, and (CF3)3COH) was investigated experimentally by the variable temperature spectroscopic methods (IR, NMR) and stopped-flow technique (UV-Vis). The structures of the hydrogen-bonded and proton transfer products were studied by DFT calculations. In agreement with the calculation results, the IR data suggest that the initial hydrogen bond is established with a hydride site for complex 1 and with the metal site for complex 2. However, no intermediate dihydrogen complex foun…

Hydrogen bondingTheoretical studyUv-vis NMR spectroscopyInorganic chemistryTransition metal polyhydridesInfrared spectroscopyProtonation010402 general chemistry01 natural sciencesProton transferMetalchemistry.chemical_compound[CHIM.COOR]Chemical Sciences/Coordination chemistrychemistry.chemical_classificationDiphenylphosphine010405 organic chemistryHydrogen bondChemistryHydrideGeneral Chemistry0104 chemical sciencesCrystallographyAcid strengthvisual_artvisual_art.visual_art_mediumIRDihydrogen complex
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Crystal structures of 2,2′-bipyridin-1-ium 1,1,3,3-tetracyano-2-ethoxyprop-2-en-1-ide and bis(2,2′-bipyridin-1-ium) 1,1,3,3-tetracyano-2-(dicyanometh…

2015

In each of the title compounds, the anion shows evidence of extensive electronic delocalization. A combination of N—H⋯N and X—H⋯N hydrogen bonds links the ions in (I) into a ribbon of alternating centrosymmetric (18) and (26) rings, and those in (II) into simple (7) chains of alternating cations and anion with further cations pendent from the chain.

Hydrogen bondingcrystal structurebipyridinium cationsCrystal structureDihedral angleRing (chemistry)Research CommunicationsIonchemistry.chemical_compoundDelocalized electronpolynitrile anionsPropaneQDGeneral Materials ScienceEthyl groupmol­ecular conformationta116Crystallographyta114Hydrogen bondCrystal structureDASGeneral ChemistryMolecular conformationhydrogen bondingQD ChemistryCondensed Matter PhysicsBipyridinium cationsCrystallographymolecular conformationMol­ecular conformationchemistryQD901-999Polynitrile anionsActa Crystallographica Section E Crystallographic Communications
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Reversible Supracolloidal Self-Assembly of Cobalt Nanoparticles to Hollow Capsids and Their Superstructures

2017

| openaire: EC/FP7/291364/EU//MIMEFUN The synthesis and spontaneous, reversible supracolloidal hydrogen bond-driven self-assembly of cobalt nanoparticles (CoNPs) into hollow shell-like capsids and their directed assembly to higher order superstructures is presented. CoNPs and capsids form in one step upon mixing dicobalt octacarbonyl (Co2CO8) and p-aminobenzoic acid (pABA) in 1,2-dichlorobenzene using heating-up synthesis without additional catalysts or stabilizers. This leads to pABA capped CoNPs (core ca. 5nm) with a narrow size distribution. They spontaneously assemble into tunable spherical capsids (d≈50-200nm) with a few-layered shells, as driven by inter-nanoparticle hydrogen bonds th…

Hydrogen bondingta221Nanoparticlechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundColloidCapsidsDicobalt octacarbonylta116ta114ChemistryHydrogen bondColloidal self-assemblyGeneral ChemistryGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesSolventCrystallographyElectron tomographycobalt nanoparticlesMagnetic nanoparticlesnanoparticlesSelf-assembly0210 nano-technologyCobaltSuperparamagnetismAngewandte Chemie
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ESI-FTICR investigation of triethylammonium ion-driven resorcin[4]arene dimer formation and structure

2002

In the course of mass spectrometric measurements a self-assembled hydrogen bonded resorcinarene dimer was observed, the formation of which was driven by the binding of triethylammonium ion as a guest and as an ionic label.

HydrogenDimerMetals and Alloyschemistry.chemical_elementIonic bondingmacromolecular substancesGeneral ChemistryResorcinarenePhotochemistryMass spectrometricCatalysisFourier transform ion cyclotron resonanceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonchemistry.chemical_compoundchemistryMaterials ChemistryCeramics and CompositesChemical Communications
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Aluminum Nanocrystals as a Plasmonic Photocatalyst for Hydrogen Dissociation

2016

Hydrogen dissociation is a critical step in many hydrogenation reactions central to industrial chemical production and pollutant removal. This step typically utilizes the favorable band structure of precious metal catalysts like platinum and palladium to achieve high efficiency under mild conditions. Here we demonstrate that aluminum nanocrystals (Al NCs), when illuminated, can be used as a photocatalyst for hydrogen dissociation at room temperature and atmospheric pressure, despite the high activation barrier toward hydrogen adsorption and dissociation. We show that hot electron transfer from Al NCs to the antibonding orbitals of hydrogen molecules facilitates their dissociation. Hot elect…

HydrogenMechanical Engineeringchemistry.chemical_elementBioengineering02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPhotochemistryAntibonding molecular orbital01 natural sciencesDissociation (chemistry)0104 chemical sciencesCatalysisMetalchemistryvisual_artPhotocatalysisvisual_art.visual_art_mediumGeneral Materials Science0210 nano-technologyPlatinumPalladiumNano Letters
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Tautomerism in pyridazin-3(2H)-one: a theoretical study using implicit/explicit solvation models.

2013

Abstract The tautomeric conversion of pyridazin-3(2H)-one 1 into pyridazin-3-ol 2 has been theoretically studied using density functional theory (DFT) methods at the B3LYP/6-311++G** level. Two mechanisms have been considered for this process: (i) one in which the hydrogen is directly transferred through TS12; and (ii) another one in which a double hydrogen transfer takes place via TS1122 upon formation of the corresponding dimer. The former requires a very high activation energy of 42.64 kcal/mol as a consequence of the strain associated with the formation of the four-membered TS12, while the latter requires a much lower activation energy, 14.66 kcal/mol. Implicit, explicit, and a combinat…

HydrogenMolecular StructureChemistryDimerSolvationchemistry.chemical_elementHydrogen BondingActivation energyModels TheoreticalComputer Graphics and Computer-Aided DesignTautomerPyridazineschemistry.chemical_compoundComputational chemistryMaterials ChemistrySolventsPolarThermodynamicsDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsSpectroscopyJournal of molecular graphicsmodelling
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Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case

2015

The association of substituted benzoates and naphthyridine dianions was used to study the complexation of dibutyltriuret. The title molecule is the simplest molecule able to form two intramolecular hydrogen bonds. The naphthyridine salt was used to break two intramolecular hydrogen bonds at a time while with the use of substituted benzoates the systematic approach to study association was achieved. Both, titrations and variable temperature measurements shed the light on the importance of conformational equilibrium and its influence on association in solution. Moreover, the associates were observed by mass spectrometry. The DFT-based computations for complexes and single bond rotational barr…

HydrogenScienceSupramolecular chemistrychemistry.chemical_elementFull Research Papersupramolecular chemistrylcsh:QD241-441QD241-441lcsh:Organic chemistryComputational chemistrysupramolekulaarinen kemiaSingle bondOrganic chemistryMoleculelcsh:Scienceta116ChemistryHydrogen bondQOrganic Chemistryassociationhydrogen bondingNMRBenzoatesChemistryIntramolecular forcelcsh:QrotamerismTitrationBeilstein Journal of Organic Chemistry
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Anharmonicity modeling in hydrogen bonded solvent dimers

2021

Abstract Harmonic and anharmonic frequencies of dimers and mixed dimers of water, methanol and benzene were computed and the results were critically analysed to investigate the anharmonicity of the normal mode vibrations within density functional theory (DFT) with empirically included Grimme correction for dispersion (D3). From several options, the B3LYP-D3/6-31++G* level of theory was selected as a good compromise between accuracy and calculation speed, suitable for future modeling of larger solvent clusters. The obtained raw harmonic and anharmonic second-order perturbation theory of vibrational frequencies (VPT2) were additionally scaled using a two-range procedure (below and above 2000 …

Hydrogenchemistry.chemical_element02 engineering and technology010402 general chemistryDFT01 natural sciencesMolecular physicsQuality (physics)Normal modePhysics::Atomic and Molecular ClustersMaterials ChemistryVPT2Physics::Chemical PhysicsPhysical and Theoretical ChemistryPerturbation theorySpectroscopyPhysicsAnharmonicity021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsFrequency scaling0104 chemical sciencesElectronic Optical and Magnetic MaterialsVibrationchemistrySolvent dimersHarmonicH-BondingDensity functional theoryAnharmonic vibrational frequencies0210 nano-technologyJournal of Molecular Liquids
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