Search results for "Intermolecular"

showing 10 items of 396 documents

Photochemistry of the H2O/CO System Revisited : The HXeOH···CO Complex in a Xenon Matrix

2017

We report on the complex of a noble-gas hydride HXeOH with carbon monoxide. This species is prepared via the annealing-induced H + Xe + OH···CO reaction in a xenon matrix, the OH···CO complexes being produced by VUV photolysis of the H2O···CO complexes. The H–Xe stretching mode of the HXeOH···CO complex absorbs at 1590.3 cm–1 and it is blue-shifted by 12.7 cm–1 from the H–Xe stretching band of HXeOH monomer. The observed blue shift indicates the stabilization of the H–Xe bond upon complexation, which is characteristic of complexes of noble-gas hydrides. The HXeOH···CO species is the first complex of a noble-gas hydride with carbon monoxide and the second observed complex of HXeOH. On the ba…

chemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencescarbon monoxidechemistry.chemical_compoundXenonmatricesNon-covalent interactionsMoleculegasesPhysical and Theoretical Chemistryta116chemistry.chemical_classificationphotochemistryHydrideIntermolecular forcePhotodissociation021001 nanoscience & nanotechnology0104 chemical sciencesMonomerchemistryH2O/CO system0210 nano-technologyCarbon monoxideJournal of Physical Chemistry C
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Role of Weak Hydrogen Bonds and Halogen Bonds in 5-Halo-1,3-dimethyluracils and Their Cocrystals—A Combined Experimental and Computational Study

2016

Seven single crystals containing either N,N-dimethyluracil (DMHU) or one of its 5-halogenated derivatives (DMXU; X = F, Cl, Br, I) were prepared using N,N-dimethylformamide as the crystallization solvent. Single crystal X-ray diffraction and quantum chemical calculations carried out at the spin component scaled local MP2 level of theory were then used to study the intramolecular halogen and nonconventional hydrogen bonds present in the structures. The results were compared to and contrasted with the previously reported data for uracil and its halogenated derivatives. In particular, the intermolecular interactions in DMIU were compared to the halogen and hydrogen bonds in 5-iodouracil that, …

computational studieshalogen bondsInorganic chemistryhydrogen bonds; computational analysis; computational studieschemistry010402 general chemistry01 natural sciencesGeneral Materials Sciencecocrystalsta116Degree of unsaturationvetysidoksetHalogen bondyhteiskiteet010405 organic chemistryHydrogen bondChemistryIntermolecular forceGeneral ChemistryCondensed Matter Physics0104 chemical sciencesSolventCrystallographycomputational analysisIntramolecular forcehydrogen bondsHalogenhalogeenisidoksetSingle crystalCrystal Growth & Design
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Conformational investigation of α,β‐dehydropeptides Part VI. Molecular and crystal structure of benzyloxycarbonylglycyl‐(Z )‐dehydrophenylalanine

1994

The structure of a peptide containing C-terminal dehydrophenylalanine, Z-Gly-(Z)-delta Phe (C19H18N2O5, MW = 354) was determined from single-crystal X-ray diffraction data. Needle-shaped crystals were grown from a 1:1 mixture of methanol-acetone in the monoclinic space group P2(1) with a = 14.717(4), b = 4.941(2), c = 12.073(4) A, beta = 103.72(4) degrees; V = 852.86(8) A3, Z = 2 and Dc = 1.32 g cm-3. The structure was solved by direct methods using SHELXS-86 and refined to a final R-index of 0.032 for 1714 observed reflections. The peptide adopts a conformation folded at the glycine residue, and principal torsion angles are omega 0 = -167.6(2) degrees, phi 1 = -71.8(3) degrees, psi 1 = -31…

conformationdehydropeptidehydrogen bondProtein ConformationChemistryHydrogen bondhelical conformersIntermolecular forceDipeptidesCrystal structuredehydrophenylalanineBiochemistryZ‐Gly‐(Z )‐APheCrystallographyProtein structureX-Ray DiffractionIntramolecular forceSpectroscopy Fourier Transform InfraredX-ray crystallographyMoleculeinfrared spectroscopyX‐ray structure analysisMonoclinic crystal systemInternational Journal of Peptide and Protein Research
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Reactivity of bis(cyclohexylammonium) 4-nitrophenylphosphate with SnMe3 Cl. X-ray structure of 4-NO2 C6 H4 PO4(SnMe3)2·H2 O

2014

The reaction of bis(cyclohexylammonium) 4-nitrophenylphosphate with Me3 SnCl (1:2) under reflux in ethanol yielded the title compound 4-NO2 C6 H4 PO4(SnMe3)2H2 O (1). The X-ray crystallographic analysis achieved on single crystals obtained by slow evaporation at room temperature revealed the formation of an unexpected supramolecular coordination network. The elementary building block can be viewed as two Me3 Sn moieties linked by a bridging 4-nitrophenylphosphate ligand. The two tin atoms are five-coordinated and describe a trans-Me3 SnO2 geometry in a trigonal bipyramidal arrangement. However, the Sn atoms are distinct, exhibiting two different environments. Thus, one is linked to two axia…

coordination-driven self-assemblyHydrogen bondChemistryStereochemistryIntermolecular forceMetals and AlloysSupramolecular chemistryX-raychemistry.chemical_elementGeneral Chemistryhydrogen bondingCondensed Matter PhysicsChemistryCrystallographyX-ray crystallographyAtomtrimethyltin(iv) 4-nitrophenylphosphatoMaterials ChemistryMoleculeTinQD1-999x-ray crystallographyMain Group Metal Chemistry
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Influences of Chemical Functionalities on Crystal Structures and Electrochemical Properties of Dihydro-benzoxazine Dimer Derivatives

2021

Dihydro-1,3,2H-benzoxazine dimer derivatives or dihydro-benzoxazine dimers are a class of compounds typically prepared by ring-opening reactions between dihydro-benzoxazines and phenols. Dihydro-benzoxazine dimers act as chelating agents for several transition and rare-earth cations. To better understand the chelating properties, it is necessary to examine their structural features and electrochemical characteristics thoroughly. However, the electrochemical properties of dihydro-benzoxazine dimers have not been tremendously examined. Herein, eight derivatives of dihydro-benzoxazine dimers possessing different substituents on the benzene ring and the tertiary-amine nitrogen were synthesized …

crystal structureCrystallographyHydrogen bondGeneral Chemical EngineeringDimerHirshfeld surfaceIntermolecular forceCrystal structureCondensed Matter PhysicsRedoxInorganic ChemistryCrystalelectrochemical propertychemistry.chemical_compoundCrystallographychemistryQD901-999General Materials SciencebenzoxazineCyclic voltammetryMethyleneCrystals
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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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Coarse-Graining Intermolecular Interactions in Dispersions of Highly Charged Colloids

2012

International audience; Effective pair potentials between charged colloids, obtained from Monte Carlo simulations of two single colloids in a closed cell at the primitive model level, are shown to reproduce accurately the structure of aqueous salt-free colloidal dispersions, as determined from full primitive model simulations by Linse et al. (Linse, P.; Lobaskin, V. Electrostatic Attraction and Phase Separation in Solutions of Like-Charged Colloidal Particles. Phys. Rev. Lett.1999, 83, 4208). Excellent agreement is obtained even when ion-ion correlations are important and is in principle not limited to spherical particles, providing a potential route to coarse-grained colloidal interactions…

endocrine systemMonte Carlo method02 engineering and technology01 natural sciencescomplex mixturesColloid0103 physical sciencesElectrochemistryGeneral Materials ScienceStatistical physicsSpectroscopyAqueous solution010304 chemical physicsChemistryIntermolecular forcedigestive oral and skin physiologySurface Chemistry and ColloidsSurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsCharged particleCondensed Matter::Soft Condensed Matter[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Chemical physicsGranularity[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyDispersion (chemistry)Pair potential
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