Search results for "Intermolecular"

showing 10 items of 396 documents

SURFACE EFFECTS ON THE GROWTH OF SOLUTION PROCESSED PENTACENE THIN FILMS

2008

13,6-N-Sulfinylacetamidopentacene (SAP) has been transferred on solid substrates both by water-rich environment and organic solvents without altering his chemical structure. Thermal conversion of SAP to pentacene leads to crystals showing similar features of vacuum-sublimated pentacene both in the bulk and thin-film phases. The thin-film phase is strongly affected by the substrate surface properties. Low energy Si-CH3 rich surfaces allow for the formation of compact micrometric crystals following a Volmer-Weber like growth with orientation suitable for field-effect carrier mobility. Screw dislocations along with straight edges are found on these systems as an indication of a loose interlaye…

Electron mobilitySpin coatingMaterials scienceIntermolecular forcecrystal growthpentacene precursorsolution depositionCrystal growthSurfaces and Interfacesspin-coatingCondensed Matter PhysicsLangmuir–Blodgett filmSurfaces Coatings and FilmsPentacenechemistry.chemical_compoundLangmuir-BlodgettchemistryChemical physicsPhase (matter)Materials ChemistryOrganic chemistryThin filmthin films pentacene electronic devices interfaces
researchProduct

Thermodynamic Interaction Parameters of Tetra-n-undecylcalix[4]resorcinarenes with Selected Solvents Studied by Inverse Gas Chromatography

2004

The basic thermodynamic parameters, characterising intermolecular interactions of tetra-n-undecylcalix[4]resorcinarene and its octaacetate derivative with simple organic solutes, were calculated by using the inverse gas chromatography method. Free energy, enthalpy and entropy of sorption were determined.

Entropy (classical thermodynamics)biologyChemistryIntermolecular forceEnthalpyInverse gas chromatographyPhysical chemistryTetraSorptionThermodynamic databases for pure substancesPhysics::Chemical PhysicsResorcinarenebiology.organism_classificationJournal of Inclusion Phenomena
researchProduct

Unveiling the Intramolecular Ionic Diels–Alder Reactions within Molecular Electron Density Theory

2021

The intramolecular ionic Diels–Alder (IIDA) reactions of two dieniminiums were studied within the Molecular Electron Density Theory (MEDT) at the ωB97XD/6-311G(d,p) computational level. Topological analysis of the electron localization function (ELF) of dieniminiums showed that their electronic structures can been seen as the sum of those of butadiene and ethaniminium. The superelectrophilic character of dieniminiums accounts for the high intramolecular global electron density transfer taking place from the diene framework to the iminium one at the transition state structures (TSs) of these IIDA reactions, which are classified as the forward electro density flux. The activation enthalpy ass…

Exergonic reaction010405 organic chemistryChemistryintramolecular ionic Diels–Alder reactionsmolecular electron density theorydieniminiumsIntermolecular forceIminiumIonic bondingGeneral Medicine010402 general chemistry01 natural sciencesElectron localization function0104 chemical sciencesGibbs free energyChemistryCrystallographysymbols.namesakeglobal electron density transferIntramolecular forcesuperelectrophilessymbolsSingle bondQD1-999Chemistry
researchProduct

Weighting non-covalent forces in the molecular recognition of C60. Relevance of concave–convex complementarity

2008

The relative contributions of several weak intermolecular forces to the overall stability of the complexes formed between structurally related receptors and [60]fullerene are compared, revealing a discernible contribution from concave–convex complementarity. Viruela Martin, Pedro Manuel, Pedro.M.Viruela@uv.es ; Viruela Martin, Rafael, Rafael.Viruela@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es

FULLERENESUNESCO::QUÍMICANon covalentBUILDING-BLOCK12-TETRACYANO-9:QUÍMICA [UNESCO]CatalysisMolecular recognitionCHEMISTRYSYSTEMSMaterials ChemistryUNESCO::QUÍMICA::Química orgánicaCARBON NANORINGSChemistryCARBON NANORINGS; BUILDING-BLOCK; FULLERENES; 11111212-TETRACYANO-910-ANTHRAQUINODIMETHANE; COMPLEXATION; DERIVATIVES; RECEPTORS; CHEMISTRY; SYSTEMSCOMPLEXATIONDERIVATIVESIntermolecular force:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysRegular polygonMolecular recognition ; Concave-convex ; Stability ; C60 ; Intermolecular forcesGeneral ChemistrySettore CHIM/06 - Chimica Organica11Intermolecular forcesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWeighting12Concave-convexbody regionsRECEPTORSC60CrystallographyChemical physicsComplementarity (molecular biology)10-ANTHRAQUINODIMETHANECeramics and CompositesMolecular recognitionStability
researchProduct

Controlling Molecular Self-Assembly on an Insulating Surface by Rationally Designing an Efficient Anchor Functionality That Maintains Structural Flex…

2013

Molecular self-assembly on surfaces is dictated by the delicate balance between intermolecular and molecule-surface interactions. For many insulating surfaces, however, the molecule-surface interactions are weak and rather unspecific. Enhancing these interactions, on the other hand, often puts a severe limit on the achievable structural variety. To grasp the full potential of molecular self-assembly on these application-relevant substrates, therefore, requires strategies for anchoring the molecular building blocks toward the surface in a way that maintains flexibility in terms of intermolecular interaction and relative molecule orientation. Here, we report the design of a site-specific anch…

Flexibility (engineering)Surface (mathematics)Materials scienceelectrostatic anchoringIntermolecular forceGeneral EngineeringGeneral Physics and AstronomyAnchoringNanotechnologyself-assembly02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciencesbulk insulatorsubstrate templatingNC-AFM0104 chemical sciencesIntermolecular interactionMolecular self-assemblyMoleculeGeneral Materials ScienceSelf-assembly0210 nano-technologyACS Nano
researchProduct

Halogen and Hydrogen Bonded Complexes of 5-Iodouracil

2013

Three derivatives of 5-iodouracil were prepared, and their complexation properties, supplemented by 5-iodouracil under the same conditions, were studied with and without halogen bond acceptors in N,N-dimethylformamide, N,N-diethylformamide, N-methylformamide, formamide, dimethylsulfoxide, and water. The intermolecular halogen and hydrogen bonding interactions observed in the solid state were investigated using single crystal X-ray diffraction and quantum chemical calculations, and the acquired data were contrasted with bonding interactions previously reported for 5-iodouracil in the Cambridge Structural Database. It was found that the polarized iodine atom and the amidic NH functionality ac…

FormamideHalogen bondvetysidoksetHydrogenHydrogen bondInorganic chemistryIntermolecular forcechemistry.chemical_element5-jodourasiili5-iodouracilGeneral ChemistryCrystal structureCondensed Matter Physicshydrogen bondingCrystallographychemistry.chemical_compoundchemistryhalogen bondingHalogenhalogeenisidoksetGeneral Materials ScienceSingle crystalta116
researchProduct

Crystal structure and Hirshfeld surface analysis of (E)-4-chloro-N-{2-[2-(4-nitro­benzyl­idene)hydrazin-1-yl]-2-oxoeth­yl}benzene­sulfonamide N,N-di­…

2018

Reaction of N-(4-chloro­benzene­sulfon­yl)glycinyl hydrazide with 4-nitro­benzaldehyde gives the N,N-di­methyl­formamide monosolvated N-acyl­hydrazone derivative, (E)-N-{2-[2-(4-nitro­benzyl­idene)- hydrazine-1-yl]-2-oxoeth­yl}-4-χhloro­benzene­sulfonamide. Rings of (10) and (11) graph-set motifs are formed in the crystal structure by N—H⋯O and C—H⋯O hydrogen bonds. The two-dimensional fingerprint (FP) plots for significant inter­molecular inter­actions indicate that the greatest contribution is from the O⋯H/H⋯O contacts (31.3%), corresponding to N⋯H⋯O/C⋯H⋯O inter­actions.

Formamidecrystal structureHydrazoneCrystal structureDihedral angle010402 general chemistry010403 inorganic & nuclear chemistryRing (chemistry)01 natural sciencesMedicinal chemistryResearch Communicationslcsh:Chemistrychemistry.chemical_compoundhydrazoneHirshfeld surface analysisGeneral Materials Sciencechemistry.chemical_classificationSchiff baseHydrogen bondinter­molecular hydrogen bondsAromaticityGeneral ChemistryCondensed Matter Physics0104 chemical sciencesintermolecular hydrogen bondslcsh:QD1-999chemistryinversion dimersActa Crystallographica Section E: Crystallographic Communications
researchProduct

Raman spectroscopy of formic acid and its dimers isolated in low temperature argon matrices

2009

Raman spectroscopy combined with matrix isolation technique was employed to study formic acid monomer and its dimers. Nine fundamentals of the HCOOH monomer were identified. Additionally, the OH torsion overtone is observed and it is engaged in Fermi resonance with the δCOH mode. Several bands of the cyclic (C2h) dimer were identified and assigned. The less stable open form (Cs) of the dimer was also present in the experiment. Three intermolecular modes for the cyclic and one mode for the open dimer were found in the low frequency region. The experimental studies were supported by harmonic and anharmonic DFT calculations.

Formic acidDimerOvertoneIntermolecular forceMatrix isolationAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_compoundsymbols.namesakeMonomerchemistryPhysics::Atomic and Molecular ClusterssymbolsPhysical chemistryCondensed Matter::Strongly Correlated ElectronsFermi resonancePhysics::Chemical PhysicsPhysical and Theoretical ChemistryRaman spectroscopyChemical Physics Letters
researchProduct

Substrate templating guides the photoinduced reaction of C60on calcite

2014

cited By 7; International audience; A substrate-guided photochemical reaction of C60 fullerenes on calcite, a bulk insulator, investigated by non-contact atomic force microscopy is presented. The success of the covalent linkage is evident from a shortening of the intermolecular distances, which is clearly expressed by the disappearance of the moiré pattern. Furthermore, UV/Vis spectroscopy and mass spectrometry measurements carried out on thick films demonstrate the ability of our setup for initiating the photoinduced reaction. The irradiation of C60 results in well-oriented covalently linked domains. The orientation of these domains is dictated by the lattice dimensions of the underlying c…

Fullerenescanning probe microscopysurface chemistry02 engineering and technologyMicroscopy Atomic Force010402 general chemistry01 natural sciencesChemical reaction530CatalysisCalcium CarbonateScanning probe microscopychemistry.chemical_compoundSpectroscopyCalcite[PHYS]Physics [physics]Spectrum AnalysisIntermolecular forcefullerenesGeneral Chemistrycovalent networksself-assemblyPhotochemical Processes021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographychemistryChemical physicsCovalent bondSelf-assembly0210 nano-technology
researchProduct

Synthesis, X-ray Structure, Conformational Analysis, and DFT Studies of a Giant s-Triazine bis-Schiff Base

2021

The current work involves the synthesis of 2,2′-(6-(piperidin-1-yl)-1,3,5-triazine-2,4-diyl)bis(hydrazin-2-yl-1-ylidene))bis(methanylylidene))diphenol 4, characterization, and the DFT studies of the reported compound. The crystal unit cell parameters of 4 are a = 8.1139(2) Å, b = 11.2637(2) Å, c = 45.7836(8) Å. The unit cell volume is 4184.28(15) Å3 and Z = 4. It crystallized in the orthorhombic crystal system and Pbca space group. The O…H, N…H, C…H, H…H and C…C intermolecular contacts which affect the crystal stability were quantitatively analyzed using Hirshfeld calculations. Their percentages were calculated to be 9.8, 15.8, 23.7, 46.4, and 1.6% from the whole contacts occurred in the cr…

General Chemical EngineeringInorganic ChemistryCrystalchemistry.chemical_compounds-triazineNBOGeneral Materials Sciencebis-Schiff basetyppiyhdisteetheterosykliset yhdisteetConformational isomerismkemiallinen synteesiSchiff baseCrystallography<i>s</i>-triazineChemistryHydrogen bondtiheysfunktionaaliteoriaIntermolecular forceconformational analysisHirshfeld analysiskiteetCondensed Matter Physics<i>bis</i>-Schiff baseCrystallographyQD901-999Intramolecular forceOrthorhombic crystal systemröntgenkristallografiaNatural bond orbitalCrystals
researchProduct