Search results for "Intermolecular"

showing 10 items of 396 documents

Decisive influence of substitution positions in molecular self-assembly

2014

Molecular self-assembly provides a versatile tool for creating functional molecular structures at surfaces. A rational design of molecular structure formation requires not only an in-depth understanding of the subtle balance between intermolecular and molecule-surface interactions, but might also involve considering chemical changes of the molecules, such as deprotonation. Here, we present a systematic investigation of a comparatively simple class of molecules, namely dihydroxybenzoic acid, which, nevertheless, enables creating a rich variety of structures when deposited onto calcite (10.4) held at room temperature. Based on non-contact atomic force microscopy measurements in ultra-high vac…

Structure formationChemistryStereochemistrySubstitution (logic)Intermolecular forceRational designGeneral Physics and AstronomyProtonation530CrystallographyDeprotonationMoleculeMolecular self-assemblyPhysical and Theoretical Chemistry
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Printing Life-Inspired Subcellular Scale Compartments with Autonomous Molecularly Crowded Confinement.

2019

A simple, rapid, and highly controlled platform to prepare life-inspired subcellular scale compartments by inkjet printing has been developed. These compartments consist of fL-scale aqueous droplets (few µm in diameter) incorporating biologically relevant molecular entities with programmed composition and concentration. These droplets are ink-jetted in nL mineral oil drop arrays allowing for lab-on-chip studies by fluorescence microscopy and fluorescence life time imaging. Once formed, fL-droplets are stable for several hours, thus giving the possibility of readily analyze molecular reactions and their kinetics and to verify molecular behavior and intermolecular interactions. Here, this pla…

Surface PropertiesDNA hairpinBiomedical EngineeringGeneral Biochemistry Genetics and Molecular BiologyFluorescenceBiomaterialsSettore CHIM/01molecular crowdingbiomolecular confinementlife-like compartmentFluorescence microscopeInkjet printinginkjet printingBiochemistry Genetics and Molecular Biology (all)ChemistryDrop (liquid)Intermolecular forceLife timeDNABiomaterialFluorescencebiomolecular confinement; DNA hairpins; inkjet printing; life-like compartments; molecular crowdingDNA hairpinslife-like compartmentsPrinting Three-DimensionalBiophysicsMolecular probeAdvanced biosystems
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A thermodynamic approach to study hydrogen-bonding interactions in solvent/solvent/polymer ternary systems

2007

Abstract A thermodynamic approach based on both the classical Flory–Huggins (FH) formalism and the association equilibria (AE) theory has been developed to study the solubility properties of a system formed by a proton-donor solvent (A), a proton-acceptor solvent (B) and a proton-acceptor polymer (C). The miscibility of this ternary system is attained by competitive specific interactions via hydrogen-bonding established between the hydroxyl and carbonyl interacting groups of either solvent–solvent (AB) or solvent–polymer (AC) system components. The binary AB and AC specific interactions and their dependence with the system composition as well as with the extent of the association equilibriu…

Ternary numeral systemPolymers and PlasticsChemistryOrganic ChemistryIntermolecular forceSolvationGeneral Physics and AstronomyEntropy of mixingGibbs free energySolventsymbols.namesakeMaterials ChemistrysymbolsPhysical chemistrySolubilityTernary operationEuropean Polymer Journal
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4-Chloro-N-methyl-N-nitroaniline

1998

The molecular structure of (p-ClC 6 H 4 )(CH 3 )NNO 2 (or C 7 H 7 ClN 2 O 2 ) contains a planar NNO 2 nitroamino group which is twisted about the N-C phenyl bond by ca 68° from the plane of the aromatic ring. The structural data are in agreement with the spectral results and indicate that there is no conjugation between the aromatic sextet and the nitroamino group. There are no specific intermolecular interactions.

Tertiary amineChemistryGroup (periodic table)StereochemistryIntermolecular forceMoleculeGeneral MedicineCrystal structureRing (chemistry)Medicinal chemistryGeneral Biochemistry Genetics and Molecular BiologyNitroanilineActa Crystallographica Section C-Crystal Structure Communications
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On the use of ionic liquids as mobile phase additives in high-performance liquid chromatography. A review.

2015

The popularity of ionic liquids (ILs) has grown during the last decades in several analytical separation techniques. Consequently, the number of reports devoted to the applications of ILs is still increasing. This review is focused on the use of ILs (mainly imidazolium-based associated to chloride and tetrafluoroborate) as mobile phase additives in high-performance liquid chromatography (HPLC). In this approach, ILs just function as salts, but keep several kinds of intermolecular interactions, which are useful for chromatographic separations. Both cation and anion can be adsorbed on the stationary phase, creating a bilayer. This gives rise to hydrophobic, electrostatic and other specific in…

TetrafluoroborateHETEROCYCLIC AROMATIC-AMINESBiochemistryHigh-performance liquid chromatographyChlorideAnalytical Chemistrychemistry.chemical_compoundSilanol suppressionAdsorptionSOLUBILIZING ABILITIES[CHIM.ANAL]Chemical Sciences/Analytical chemistryPhase (matter)medicineEnvironmental ChemistryOrganic chemistryOptimisationSpectroscopyHALF-WIDTH PLOTSMechanisms of retentionOVERLOADED BAND PROFILESANALYTICAL-CHEMISTRYSILANOL-SUPPRESSING POTENCYHYDROCARBONACEOUS STATIONARY PHASESIntermolecular forceAdditivesHigh-performance liquid chromatographyIonic liquidsSilanolROOM-TEMPERATURERETENTION MECHANISMChemical engineeringchemistryRP-HPLCIonic liquidmedicine.drugAnalytica chimica acta
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Supramolecular self-assembly on the B-Si(111)-(√3x√3) R30° surface: From single molecules to multicomponent networks

2017

Abstract Understanding the physical and chemical processes in which local interactions lead to ordered structures is of particular relevance to the realization of supramolecular architectures on surfaces. While spectacular patterns have been demonstrated on metal surfaces, there have been fewer studies of the spontaneous organization of supramolecular networks on semiconductor surfaces, where the formation of covalent bonds between organics and adatoms usually hamper the diffusion of molecules and their subsequent interactions with each other. However, the saturation of the dangling bonds at a semiconductor surface is known to make them inert and offers a unique way for the engineering of m…

Two-dimensional molecular networkSupramolecular chemistryNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesLondon dispersion forcelaw.invention[SPI.MAT]Engineering Sciences [physics]/MaterialsMultiscale modellinglawMaterials ChemistryMolecule[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsScanning tunneling microscopyTopology (chemistry)[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]ChemistryIntermolecular forceSemiconductor surfacesMetals and AlloysDangling bondSurfaces and InterfacesGeneral ChemistrySelf-assembly Intermolecular forces021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSelf-assemblyScanning tunneling microscope0210 nano-technology
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New insights in chemical reactivity from quantum chemical topology.

2021

International audience; Based on the quantum chemical topology of the modified electron localization function ELFx, an efficient and robust mechanistic methodology designed to identify the favorable reaction pathway between two reactants is proposed. We first recall and reshape how the supermolecular interaction energy can be evaluated from only three distinct terms, namely the intermolecular coulomb energy, the intermolecular exchange‐correlation energy and the intramolecular energies of reactants. Thereafter, we show that the reactivity between the reactants is driven by the first‐order variation in the coulomb intermolecular energy defined in terms of the response to changes in the numbe…

Water dimerQuantum Chemical TopologyMaterials science010304 chemical physicsHydrogen bondIntermolecular forceGeneral ChemistryInteraction energy010402 general chemistryTopology01 natural scienceselectrophile0104 chemical sciencesComputational Mathematicselectron localization functionIntramolecular force0103 physical sciences[CHIM]Chemical SciencesMoleculeChemical ReactivityFrontier Molecular Orbital Theory[INFO]Computer Science [cs]Reactivity (chemistry)nucleophileTopology (chemistry)Journal of computational chemistryREFERENCES
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Rotational coherence imaging and control for CN molecules through time-frequency resolved coherent anti-Stokes Raman scattering

2011

Numerical wave packet simulations are performed for studying coherent anti-Stokes Raman scattering (CARS) for CN radicals. Electronic coherence is created by femtosecond laser pulses between the X²Σ and B²Σ states. Due to the large energy separation of vibrational states, the wave packets are superpositions of rotational states only. This allows for a specially detailed inspection of the second- and third-order coherences by a two-dimensional imaging approach. We present the time-frequency domain images to illustrate the intra- and intermolecular interferences, and discuss the procedure to rationally control and experimentally detect the interferograms in solid Xe environment. peerReviewed

Wave packetvibraatiotilatGeneral Physics and Astronomyrotaatiotilatvapaat radikaalit01 natural sciencesMolecular physicslaw.inventionsymbols.namesakeNuclear magnetic resonancecoherent antiStokes Raman scatteringlaw0103 physical sciencesCoherent anti-Stokes Raman spectroscopyPhysical and Theoretical Chemistry010306 general physicsta116010304 chemical physicsta114rotationla statesChemistryIntermolecular forcekoherentti anti-Stokes Raman spektroskopiaLaserTime–frequency analysisFemtosecondsymbolshiiliyhdisteetcarbon comboundsnumeerinen analyysivibrational statesRaman scatteringCoherence (physics)The Journal of Chemical Physics
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Theoretical characterization of the photochemical reaction CO2+O(3P)→CO+O2 related to experiments in solid krypton

2020

Formation and decomposition of the complex of carbon dioxide and atomic oxygen are characterized by quantum chemistry methods aiming to rationalize experimental studies in solid krypton. The observed FTIR spectra reflected the temporal evolution of the system after irradiation showing the bands of reactants, intermediates and products. Advanced quantum chemistry calculations show that the T-shape complex CO2…O(3P) can be formed in the matrix. Its excitation by the 193 nm light results in the charge-transfer state CO2+…O-, which evolves to the reaction intermediate CO3. The latter species decomposes to CO + O2 following pathways on the excited state energy surfaces. peerReviewed

atomic oxygenquantum chemistryhiilidioksidiphotochemistryhappikvanttikemiacarbon dioxidematrix isolationmolekyylitintermolecular complexesvalokemiaexcited states
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Theoretical and experimental studies of some main group compounds : from closed shell interactions to singlet diradicals and stable radicals

2012

Acquiring knowledge of different interactions within and between molecules is a fascinating undertaking as it not only deepens our understanding of chemical bonding but also offers insight into electronic structures, molecular properties and the connections between these two. This dissertation combines together three main group chemistry related topics within the aforementioned theme. Research presented in the first third of this dissertation describes wave function and density functional theory studies of weak inter- and intramolecular interactions in pnictogen-based dimers X3Pn···PnX3 (Pn = N-Bi; X = F-I), dithallenes RTlTlR (R = H, Me, tBu, Ph) and octachalcogen dications Ch82+ (Ch = S, …

atomitkemialliset sidoksetstable radicalssynthesisintermolecular interactionskemiatheoretical and computational chemistrysinglet diradical characterintramolecular interactionsmolekyylitsynteesimain group chemistryclosed shell interactions
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