Search results for "bond"

showing 10 items of 3527 documents

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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Iodinatedortho-Carboranes as Versatile Building Blocks to Design Intermolecular Interactions in Crystal Lattices

2009

[EN] The crystal structures of numerous iodinated ortho-carboranes have been studied, which has revealed the diversity of intermolecular interactions that these substances can adopt in the solid state. The nature-mostly as it relates to hydrogen and/or halogen bonds-and relative strength of such interactions can be adjusted by selectively introducing substituents onto the cluster, thus enabling the rational design of crystal lattices. In this work we present the newly determined crystal structures of the following iodinated ortho-carboranes: 9-I-1,2-closo-C2B10H11, 4,5,7,8,9,10,11,12-I-8-1,2-closo-C2B10H4, 3,4,5,6,7,8,9,10,11,12-I-10,-1,2-closo-C2B10H2, 1-Me-8,9,10,12-I-4-1,2-closo-C2B10H7,…

HydrogenStereochemistrySupramolecular chemistryCrystal engineeringchemistry.chemical_elementCrystal structure010402 general chemistryCrystal engineering01 natural sciencesCatalysisHydrogen bondsHalogensQUIMICA ANALITICACluster (physics)Carboranes010405 organic chemistryChemistryHydrogen bondOrganic ChemistryIntermolecular forceGeneral Chemistry0104 chemical sciencesCrystallographyHalogenSupramolecular chemistryChemistry - A European Journal
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Host-Guest Complexes of C-Ethyl-2-methylresorcinarene and Aromatic N,N′-Dioxides

2017

The C‐ethyl‐2‐methylresorcinarene (1) forms 1:1 in‐cavity complexes with aromatic N,N′‐dioxides, only if each of the aromatic rings has an N−O group. The structurally different C‐shaped 2,2′‐bipyridine N,N′‐dioxide (2,2′‐BiPyNO) and the linear rod‐shaped 4,4′‐bipyridine N,N′‐dioxide (4,4′‐BiPyNO) both form 1:1 in‐cavity complexes with the host resorcinarene in C4v crown and C2v conformations, respectively. In the solid state, the host–guest interactions between the 1,3‐bis(4‐pyridyl)propane N,N′‐dioxide (BiPyPNO) and the host 1 stabilize the unfavorable anti‐gauche conformation. Contrary to the N,N′‐dioxide guests, the mono‐N‐oxide guest, 4‐phenylpyridine N‐oxide (4PhPyNO), does not form an…

HydrogenStereochemistrySupramolecular chemistryNN′-dioxideschemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistryBipyridinechemistry.chemical_compoundN′-dioxidessupramolekulaarinen kemiaConformationWeak interactionsta116ta114Resorcinarenes010405 organic chemistryHydrogen bondAromaticityGeneral ChemistryResorcinareneN0104 chemical scienceschemistryDeuteriumMethanolSupramolecular chemistry
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Effect of a Rigid Sulfonamide Bond on Molecular Folding: A Case Study

2015

A disulfonamide compound with bulky aromatic side chains was prepared, and its properties as a potential building block for foldamers were evaluated. Two different solvate crystal forms of the compound were identified and compared to the structures of an analogous oligoamide and related disulfonamides. The disulfonamide is unfolded in one of the solvates, whereas in the other one, a loosely folded conformer stabilized by an intramolecular hydrogen bond is found. Density functional calculations indicated that the loosely folded conformer is slightly more stable than its unfolded isomer. The calculations also identified a third, more tightly folded and more extensively hydrogen bonded, confor…

HydrogenStereochemistrychemistry.chemical_elementmolecular foldingkonformeeritorgaaninen synteesiCrystalSide chainmolecular conformersGeneral Materials Sciencemolekyylien laskostuminenta116sulfonamidisidosConformational isomerismX-ray crystallographychemistry.chemical_classificationHydrogen bondsulfonamide bondGeneral Chemistryorganic synthesisCondensed Matter PhysicsSulfonamideFolding (chemistry)chemistryIntramolecular forceröntgenkristallografiaCrystal Growth & Design
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ChemInform Abstract: Exploring the 2,2′-Diamino-5,5′-bipyrimidine Hydrogen-Bonding Motif: A Modular Approach to Alkoxy-Functionalized Hydrogen-Bonded…

2010

The programmed self-association of 2,2’-diamino-4,4’-dialkoxy-5,5’-bipyrimidines allows for the de novo construction of alkoxy-functionalized H-bonded ribbons and sheets as evidenced by X-ray crystallographic analysis. The data provide insight into the interplay of the different structural and interactional features of the molecular components to the generation of the supramolecular assembly. Hydrophobicity of the didodecyl side chains of 4c leads to the dominance of the H-bonding factor, resulting in the formation of a fully interconnected array. These results define the utility of the of 2,2’-diamino-4,4’-dialkoxy-5,5’-bipyrimidines as a potential scaffold for the attachment of electro- o…

Hydrogenbusiness.industryChemistryHydrogen bondAlkoxy groupSupramolecular chemistrySide chainchemistry.chemical_elementGeneral MedicineModular designbusinessCombinatorial chemistrySupramolecular assemblyChemInform
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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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Systematic Construction of Ternary Cocrystals by Orthogonal and Robust Hydrogen and Halogen Bonds

2016

A carefully designed strategy is presented for the construction of ternary cocrystals, based on the orthogonality of two supramolecular interaction modes: hydrogen bonding between crown ethers and thioureas and the halogen bonding between thioureas and perfluorohalocarbons. Tested on a set comprising two crown ethers, two thioureas and five halogen bond donors, the strategy resulted in a high, 75% success rate, with 15/20 component combinations yielding at least one cocrystal. Crystal structure analysis revealed the interplay between the hydrogen and halogen bonding motifs, also shedding light on the variables affecting their formation. peerReviewed

Hydrogenkemiahalogen bondsSupramolecular chemistrychemistry.chemical_elementCrystal structure010402 general chemistrychemistry01 natural sciencesBiochemistryCocrystalCatalysisColloid and Surface ChemistryOrganic chemistryta116Halogen bond010405 organic chemistryChemistryHydrogen bondGeneral Chemistry0104 chemical sciencesternary cocrystalsCrystallographyvetyhydrogenHalogenTernary operation
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New indications for the potential involvement of C–F-bonds in hydrogen bonding

2006

Abstract Solid state structures of a selection of 2-fluoro-2-phenylcyclopropane derivatives were examined by X-ray crystallography in order to identify short intermolecular contacts of C–F groups to H–X moieties (X=C, N). Particularly, several cis -configured fluorinated phenylcyclopropane derivatives showed extremely close intermolecular contacts. The shortest of such C–H⋯F–C-distances (2.17 A, C–F–H angle 162°) was found in (1 S ,2 R )-(2-fluoro-2-phenylcyclopropyl)methyl N -(4-bromophenyl)carbamate ( 8 ) and the closest N–H⋯F–C-interaction (2.01 A, C–F–H angle 167°) was found in (±)- cis -2-fluoro-2-phenylcyclopropyl carboxamide ( 4 ). Comparison of the structures of several of the fluor…

Hydrogenmedicine.drug_classStereochemistryHydrogen bondOrganic ChemistryIntermolecular forceSolid-statechemistry.chemical_elementCarboxamideAnalytical ChemistryInorganic ChemistryCrystalCrystallographychemistryFluorinemedicineEnantiomerSpectroscopyJournal of Molecular Structure
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