Search results for "intermolecular interaction"

showing 10 items of 32 documents

Brownian dynamics simulation of grafted polymer brushes

1995

We present results of computer simulations by the method of Brownian dynamics of polymeric brushes attached to impenetrable planes. For testing both model and method we have used one polymer brush attached to a repulsive plane and compare some results with Monte Carlo results of Lai and Binder on the bond fluctuation model. We have also studied two polymeric brushes attached to two parallel planes at different distances between planes, and investigate the interplay between the interpenetration of the brushes and the configurational properties of the grafted chains.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsChemistryPlane (geometry)Organic ChemistryMonte Carlo methodPolymerCondensed Matter PhysicsPolymer brushdigestive systemCondensed Matter::Soft Condensed MatterInorganic ChemistryComputer Science::GraphicsIntermolecular interactionChemical physicsMaterials ChemistryBrownian dynamicsStatistical physicsStructure factorBond fluctuation modelMacromolecular Theory and Simulations
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Crystal structure, Hirshfeld surface analysis and HOMO–LUMO analysis of (E)-4-bromo-N′-(4-methoxybenzylidene)benzohydrazide

2018

The title Schiff base compound, C15H13BrN2O2, displays an E configuration with respect to the C=N double bond, which forms a dihedral angle of 58.06 (9)° with the benzene ring. In the crystal, the molecules are linked into chains parallel to the b axis by N—H...O and C—H...O hydrogen bonds, giving rise to rings with an R 2 1(6) graph-set motif. The chains are further linked into a three-dimensional network by C—H...π interactions. A Hirshfeld surface analysis indicates that the most important contributions to the crystal packing are from C...H (33.2%), H...H (27.7%), Br...H/H...Br (14.2%) and O...H/H...O (13.6%) interactions. The title compound has also been characterized by frontier molecu…

crystal structureDouble bondCrystal structureDihedral angle010402 general chemistryRing (chemistry)01 natural sciencesCrystalSchiff basechemistry.chemical_compoundHirshfeld surface analysisGeneral Materials ScienceHOMO/LUMOchemistry.chemical_classificationCrystallographySchiff baseintermolecular interactions010405 organic chemistryHydrogen bondGeneral ChemistryCondensed Matter Physics0104 chemical sciencesCrystallographyHOMO–LUMO calculationchemistryQD901-999Acta Crystallographica Section E Crystallographic Communications
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Crystal structure, Hirshfeld surface analysis and HOMO–LUMO analysis of (E)-N′-(3-hydroxy-4-methoxybenzylidene)nicotinohydrazide monohydrate

2019

The title Schiff base compound displays an E configuration with respect to the C=N double bond. The pyridine and benzene rings subtend a dihedral angle of 29.63 (7)°. In the crystal, the mol­ecules are linked by N—H⋯O, C—H⋯O, O—H⋯O and O—H⋯N hydrogen-bonding inter­actions.

crystal structureSchiff baseCrystallographyintermolecular interactionsSupramolecular chemistryGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsResearch CommunicationsCrystalchemistry.chemical_compoundCrystallographySchiff basechemistryQD901-999PyridineHirshfeld surface analysisGeneral Materials ScienceBenzeneinter­molecular inter­actionsHOMO/LUMOActa Crystallographica Section E: Crystallographic Communications
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Intramolecular 1,5-S...N σ-hole interaction in (E)-N′-(pyridin-4-ylmethylidene)thiophene-2-carbohydrazide

2020

The hydrazide-hydrazone forms inverse dimers via hydrogen bonding, but its conformation is defined by the presence of an intra­molecular chalcogen bond. Electrostatic forces dominate in the crystal packing and give rise to a layered supra­molecular structure.

crystal structurehirshfeld surfaceDouble bondImineStackingCrystal structureCarbohydrazide010402 general chemistryRing (chemistry)01 natural sciencesResearch Communicationsenergy frameworkslcsh:Chemistrychemistry.chemical_compoundchalcogen bondingGeneral Materials Sciencechemistry.chemical_classificationQuantitative Biology::Biomoleculesintermolecular interaction energies010405 organic chemistryHydrogen bondGeneral Chemistryinter­molecular inter­action energieshydrogen bondingCondensed Matter Physics4-pyridinecarboxaldehyde 2-thienyl hydrazone0104 chemical sciencesCrystallographylcsh:QD1-999chemistry4-pyridine­carboxaldehyde 2-thienyl hydrazoneMonoclinic crystal systemActa Crystallographica Section E Crystallographic Communications
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Bis{4-[(2-hydroxy-5-methoxy-3-nitrobenzylidene)amino]phenyl} ether

2020

The mol­ecule of the title oxybis compound lies on a twofold rotational axis. The conformation of the title compound is discussed and compared to those of related structures. In the crystal, mol­ecules of the title compound are assembled into layers parallel to the ab plane through C—H⋯O hydrogen bonds.

crystal structureinter­molecular inter­actionImineEtherCrystal structureDihedral angle010402 general chemistry010403 inorganic & nuclear chemistryRing (chemistry)01 natural sciencesResearch Communicationschemistry.chemical_compoundGeneral Materials SciencePhysics::Chemical PhysicsBenzeneoxybis schiff baseCrystallographyChemistryHydrogen bondGeneral Chemistryintermolecular interactionCondensed Matter Physics0104 chemical sciencesCrystallographyQD901-999NitroActa Crystallographica Section E Crystallographic Communications
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The Effect of the Side Chain on Gelation Properties of Bile Acid Alkyl Amides

2021

Abstract Six bile acid alkyl amide derivatives were studied with respect to their gelation properties. The derivatives were composed of three different bile acids with hexyl or cyclohexyl side chains. The gelation behaviour of all six compounds were studied for 36 solvents with varying polarities. Gelation was observed mainly in aromatic solvents, which is characteristic for bile‐acid‐based low molecular weight gelators. Out of 108 bile acid‐solvent combinations, a total of 44 gel systems were formed, 28 of which from lithocholic acid derivatives, only two from deoxycholic acid derivatives, and 14 from cholic acid derivatives. The majority of the gel systems were formed from bile acids with…

geelitintermolecular interactionssupramolecular gelssolvent influenceCholic AcidAmidesBile Acids and Saltssappihapotamiditbile acid amidessupramolekulaarinen kemiaLithocholic AcidGelsResearch ArticlesröntgenkristallografiaResearch ArticleX-ray crystallography
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Halogen Bonds in Square Planar 2,5-Dihalopyridine-Copper(II) Bromide Complexes

2018

halogeenitintermolecular interactions010405 organic chemistryIntermolecular forcestructure elucidationchemistry.chemical_elementkuparikompleksiyhdisteet010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic ChemistryCopper(II) bromidechemistry.chemical_compoundCrystallographyPlanarchemistrycopperHalogenhalogensSquare (unit)bromiditta116European Journal of Inorganic Chemistry
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Experimental FTIR-MI and Theoretical Studies of Isocyanic Acid Aggregates

2023

Homoaggregates of isocyanic acid (HNCO) were studied using FTIR spectroscopy combined with a low-temperature matrix isolation technique and quantum chemical calculations. Computationally, the structures of the HNCO dimers and trimers were optimized at the MP2, B3LYPD3 and B2PLYPD3 levels of theory employing the 6-311++G(3df,3pd) basis set. Topological analysis of the electron density (AIM) was used to identify the type of non-covalent interactions in the studied aggregates. Five stable minima were located on the potential energy surface for (HNCO)2, and nine were located on the potential energy surface for (HNCO)3. The most stable dimer (D1) involves a weak, almost linear N-H⋯N hydrog…

hydrogen bondatmospheric chemistryvetysidoksetOrganic ChemistryspektroskopiaPharmaceutical ScienceHNCOintermolecular interactionlaskennallinen kemiasolid argoncomputational chemistrymatrix isolation (MI)vibrational spectroscopyAnalytical Chemistryilmakemiamolecular complexChemistry (miscellaneous)Drug DiscoveryMolecular MedicinePhysical and Theoretical ChemistryFourier transform infrared (FTIR)Molecules
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Self-assembly mechanism based on charge density topological interaction energies

2017

The packing interactions have been evaluated in the context of the self-assembly mechanism of crystal growth and also for its impacts on the aromaticity of the trimesate anion. The structure of ethylammonium trimesate hydrate (1) measured at 100 K and a charge density model, derived in part from theoretical structures, is reported. Theoretical structure factors were obtained from the geometry-optimized periodic wave function. The trimesic acid portion of 1 is fully deprotonated and participates in a variety hydrogen bonding motifs. Topological analysis of the charge density model reveals the most significant packing interactions and is then compared to a complementary analysis performed by …

intermolecular interactions010405 organic chemistryChemistryHydrogen bondsupramolecular synthonsIntermolecular forceCharge densityAromaticityContext (language use)010402 general chemistryCondensed Matter PhysicsTopology01 natural sciences0104 chemical sciencestopological analysischemistry.chemical_compoundcharge densitySelf-assemblyTrimesic acidPhysical and Theoretical ChemistryHydrateStructural Chemistry
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Halogen Bonds in Square Planar 2,5-Dihalopyridine-Copper(II) Bromide Complexes

2018

Halogen bonding in self-complementary 1:2 metal–ligand complexes obtained from copper(II) bromide (CuBr2) and seven 2,5-dihalopyridines were analyzed using single-crystal X-ray diffraction. All presented discrete complexes form 1D polymeric chains connected with C–X···Br–Cu halogen bonds (XB). In (2-chloro-5-X-pyridine)2·CuBr2 (X = Cl, Br, and I) only the C5-halogen and in (2-bromo-5-X-pyridine)2·CuBr2 (X = Cl, Br, and I) both C2- and C5-halogens form C–X···Br–Cu halogen bonds with the X acting as the XB donor and copper-coordinated bromide as the XB acceptor. The electron-withdrawing C2-chloride in (2-chloro-5-X-pyridine)2·CuBr2 complexes has only a minor effect on the C5–X5···Br–Cu XBs, a…

intermolecular interactionshalogeenitstructure elucidationbromiditkuparikompleksiyhdisteet
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