Search results for "molecular symmetry"

showing 9 items of 29 documents

Chemistry of density : extension and structural origin of Carnelley's rule in chloroethanes

2012

Low-density liquids and solids, with all intermolecular contacts longer than the sum of van der Waals radii, are formed by all ethanes chlorinated at one locant: CH2ClCH3, CHCl2CH3 and CCl3CH3. The concepts of molecular symmetry described by Carnelley and that of point groups have been compared. Carnelley's rule, when applied to liquid and solid chloroethanes clearly reveals the density dependence on the presence of intermolecular Cl⋯Cl and H⋯Cl short contacts, or their absence due to steric hindrances of overcrowded substituents. At 2.62 GPa, CH2ClCH3 freezes directly into phase II, with molecules arranged into layers with short Cl⋯Cl, H⋯Cl and H⋯H contacts. Only for CH2ClCH3, both the low…

Steric effectsChemistryIntermolecular forceGeneral ChemistryCondensed Matter PhysicsPoint groupLocantsymbols.namesakeComputational chemistryChemical physicsPhase (matter)Molecular symmetrysymbolsMoleculeGeneral Materials ScienceVan der Waals radiusCrystEngComm
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Halogen...halogen interactions in pressure-frozen ortho- and meta-dichlorobenzene isomers.

2007

Isomers 1,2-dichlorobenzene (o-DCB) and 1,3-dichlorobenzene (m-DCB) were high-pressure frozen in-situ in a Merrill–Bassett diamond–anvil cell and their structures determined at room temperature and at 0.18 (5) GPa for o-DCB, and 0.17 (5) GPa for m-DCB by single-crystal X-ray diffraction. The patterns of halogen...halogen intermolecular interactions in these structures can be considered to be the main cohesive forces responsible for the molecular arrangements in these crystals. The molecular packing of dichlorobenzene isomers, including three polymorphs of 1,4-dichlorobenzene (p-DCB), have been compared and relations between their molecular symmetry, packing arrangements, intermolecular inte…

Steric effectspressure-crystallization methodhigh-pressure crystal structureStereochemistryChemistryIntermolecular forcehalogen...halogen intermolecular interactionsstructure-property relationsGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular BiologyDichlorobenzeneCrystallographyMolecular geometryMolecular symmetryMelting pointMoleculeActa crystallographica. Section B, Structural science
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Bond-based 3D-chiral linear indices: Theory and QSAR applications to central chirality codification

2008

The recently introduced non-stochastic and stochastic bond-based linear indices are been generalized to codify chemical structure information for chiral drugs, making use of a trigonometric 3D-chirality correction factor. These improved modified descriptors are applied to several well-known data sets to validate each one of them. Particularly, Cramer's steroid data set has become a benchmark for the assessment of novel quantitative structure activity relationship methods. This data set has been used by several researchers using 3D-QSAR approaches such as Comparative Molecular Field Analysis, Molecular Quantum Similarity Measures, Comparative Molecular Moment Analysis, E-state, Mapping Prope…

Stochastic ProcessesQuantitative structure–activity relationshipIndolesProperty (programming)ChemistryComparabilityQuantitative Structure-Activity RelationshipAngiotensin-Converting Enzyme InhibitorsStereoisomerismGeneral ChemistrySet (abstract data type)Data setComputational MathematicsModels ChemicalPiperidinesComputational chemistryDrug DesignBenchmark (computing)Molecular symmetryCombinatorial Chemistry TechniquesReceptors sigmaThermodynamicsTrigonometryAlgorithmJournal of Computational Chemistry
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Key Role of the Cation in the Crystallization of Chiral Tris(Anilato)Metalate Magnetic Anions

2015

A complete study of the role played by the usually considered “innocent” cation in the synthesis of chiral tris(anilato)metalate magnetic complexes is presented. This study is based on the rational synthesis of the family of compounds formulated as A3[MIII(C6O4X2)3] with A+ = [PPh3Et]+, [PPh3Pr]+, [PBu4]+, [NHep4]+, and [PPh4]+; MIII = CrIII, FeIII, and GaIII; and [C6O4X2]2– (X = Cl, Br, and NO2; [C6O4X2]2– = dianion of the 3,6-disubstituted derivatives of 2,5-dihydroxy-1,4-benzoquinone, H4C6O4). We show and explain the unexpected key role played by the cations in isolating chiral or achiral crystals of these [MIII(C6O4X2)3]3– anions with D3 point group symmetry. Thus, among the 18 new comp…

Tris010405 organic chemistryStereochemistryChemistryGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceslaw.inventionCrystallographychemistry.chemical_compoundlawMolecular symmetryGeneral Materials ScienceCrystallizationCrystal Growth & Design
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On the study of the vibrational energy levels of Arsine molecule

2008

Abstract We compare two formalisms applied to the vibrational modes of the molecule of AsH 3 of C 3 v molecular symmetry group. Indeed, the close stretching modes of this molecule may be considered as those of a three-dimensional oscillator whereas the bending modes may be considered either as a one-dimensional oscillator of symmetry A 1 and a two-dimensional oscillator of symmetry E or as an approximate three-dimensional oscillator. So, we have applied the U ( p  + 1) formalism to the both stretching and bending modes and introduced coupling terms acting on an appropriate coupled vibrational basis through a local mode formalism. We have then compared the result of our fitting with those ob…

Unitary group approachVibrational energy[ PHYS.QPHY ] Physics [physics]/Quantum Physics [quant-ph]02 engineering and technology01 natural sciencesHot bandchemistry.chemical_compoundArsine[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Normal mode0103 physical sciencesMolecular symmetryMoleculePhysical and Theoretical Chemistry010306 general physicsSpectroscopyPhysicsVibrational excitationsLocal modeNormal mode021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsVibrationchemistryMolecular vibrationAsH3Atomic physics0210 nano-technology
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Properties and interactions – melting point of tri­bromo­benzene isomers

2021

The melting points of tri­bromo­benzene isomers are correlated with the number, nature and distribution of intermolecular interactions in their structures.

chemistry.chemical_classificationHalogen bondtribromobenzene isomersChemistryIntermolecular forcemelting pointMetals and AlloysClose-packing of equal spheresResearch PapersAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsCrystalmolecular symmetryCrystallographynoncovalent interactionsMaterials ChemistryMelting pointMolecular symmetrystructure-property relationshipNon-covalent interactionsMoleculehalogen bondActa Crystallographica Section B-Structural Science Crystal Engineering and Materials
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Melting point, molecular symmetry and aggregation of tetrachlorobenzene isomers: the role of halogen bonding

2018

Tetrachlorobenzenes represent one of the best known, but not yet fully understood, group of isomers of the structure–melting point relationship. The differences in melting temperatures of these structurally related compounds were rationalized in terms of the hierarchy and nature of formed noncovalent interactions, and the molecular aggregation that is influenced by molecular symmetry. The highest melting point is associated with the highly symmetric 1,2,4,5-tetrachlorobenzene isomer. The structures of less symmetrical 1,2,3,4-tetrachlorobenzene and 1,2,3,5-tetrachlorobenzene, determined at 270 and 90 K, show a distinct pattern of halogen bonds, characterized by the different numbers and typ…

melting pointEnthalpy02 engineering and technology010402 general chemistry01 natural sciencesGroup (periodic table)Materials ChemistryMolecular symmetryNon-covalent interactionschemistry.chemical_classificationHalogen bondstructure–property relationsIntermolecular forceMetals and Alloys021001 nanoscience & nanotechnologytetra­chloro­benzene isomersAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialsmolecular symmetryCrystallographychemistryhalogen bondingHalogenMelting point0210 nano-technologyActa Crystallographica Section B Structural Science, Crystal Engineering and Materials
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Response to comment on Properties and inter­actions – melting point of tri­bromo­benzene isomers

2022

molecular symmetrycohesion forcesmelting pointisomersActa Crystallographica Section B-Structural Science Crystal Engineering and Materials
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Symmetry breaking in ligand-protected gold clusters probed by nonlinear optics

2016

The first hyperpolarizabilities of [Au25(SR)18](-1/0) and Au38(SR)24 clusters were determined by Hyper-Rayleigh Scattering. A strong dependence on the molecular symmetry was observed, and we explore two strategies to destroy the center of inversion in [Au25(SR)18](-1/0), protection by chiral ligands and alloying of the cluster with silver. This may open new avenues to applications of Au : SR clusters in second-order nonlinear optics.

ta114Condensed matter physicsligandsChemistryScatteringLigandnonlinear opticsNonlinear optics02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologygold clusters01 natural sciencesMolecular physics0104 chemical sciencesmolecular symmetryMolecular symmetryCluster (physics)General Materials ScienceSymmetry breaking0210 nano-technologyta116Nanoscale
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