Search results for "Molecular symmetry"

showing 10 items of 29 documents

Applications of Bond-Based 3D-Chiral Quadratic Indices in QSAR Studies Related to Central Chirality Codification

2009

The concept of bond-based quadratic indices is generalized to codify chemical structure information for chiral drugs, making use of a trigonometric 3D-chirality correction factor. In order to evaluate the effectiveness of this novel approach in drug design, we have modeled several well-known data sets. In particularly, Cramer's steroid data set has become a benchmark for the assessment of novel QSAR methods. This data set has been used by several researchers using 3D-QSAR approaches. Therefore, it is selected by us for the shake of comparability. In addition, to evaluate the effectiveness of this novel approach in drug design, we model the angiotensin-converting enzyme inhibitory activity o…

Quantitative structure–activity relationshipTheoretical computer scienceComputer scienceChemistryOrganic ChemistryComparabilityComputer Science ApplicationsData setSet (abstract data type)Quadratic equationComputational chemistryDrug DiscoveryMolecular symmetryBenchmark (computing)TrigonometryQSAR & Combinatorial Science
researchProduct

Tetra-p-tolyl-verbindungen p-Tol4Si und p-Tol4Ge: Ein beitrag zur konfiguration der tetraaryl-methan-analoga Ar4M (M = C, Si, Ge, Sn, Pb)

1992

Abstract p-Tol4Si and p-Tol4Ge have been obtained from the reaction of p-TolLi with SiCl4 and of p-TolMgBr with GeCl4, respectively. The crystal structures have been determined and compared with those of the homologous compounds p-Tol4Sn and p-Tol4Pb. The latter two molecules (space group I 4 ) exhibit a S4 axis running between the aromatic groups and are shortened along this axis: all four p-Tol groups are closer together than in an undistorted tetrahedron. In the cases of the silane and germane (space group Pc), the tetrahedron is lengthened along one of the bond axes CM: only three of the four p-Tol groups are closer together, and the set up of a special molecular symmetry is blocked. A…

StereochemistryOrganic ChemistryCrystal structureCarbon-13 NMRBiochemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyAtomic radiuschemistryGroup (periodic table)GermaneMaterials ChemistryTetrahedronMolecular symmetryMoleculePhysical and Theoretical ChemistryJournal of Organometallic Chemistry
researchProduct

Molecular association in low-temperature and high-pressure polymorphs of 1,1,1,2-tetrachloroethane

2010

Interactions and aggregation of 1,1,1,2-tetrachloroethane molecules, Cl3CCH2Cl, have been investigated at low temperature and high pressure. Isobaric and isochoric crystallizations led to two polymorphs, characterized by single-crystal X-ray diffraction. The low-temperature polymorph α is monoclinic, space group C2/c, with molecules orientationally disordered in two sites at the temperature independent 70:30 rate. In isothermal conditions (295 K) 1,1,1,2-tetrachloroethane freezes at 0.73 GPa. The high-pressure polymorph β is monoclinic, space group P21/c, with the molecules fully ordered. The molecular aggregation at varied thermodynamic conditions results from the interplay of halogen inte…

CrystallographyIsochoric processChemistryIntermolecular forceMolecular symmetryMelting pointMoleculeIsobaric processGeneral Materials ScienceGeneral ChemistryCondensed Matter PhysicsIsothermal processMonoclinic crystal systemCrystEngComm
researchProduct

Does Ligand Symmetry Play a Role in the Stabilization of DNA G-Quadruplex Host-Guest Complexes?

2014

In efforts to find agents with improved biological activity against cancer cells, recent years have seen an increased interest in the study of small molecules able to bind the deoxyribonucleic acid (DNA) when it assumes secondary structures known as G-quadruplexes (G4s) preferring them over the B form. Currently, several compounds reported in literature have already shown to be good candidates as G4s DNA stabilizers. Even though some specific features for the G4s affinity are known, such as a π-delocalized system able to stack at the top/end of a G-tetrad and positively charged substituents able to interact with the grooves, it is not clear yet what kind of structural features affect more t…

PharmacologyGene isoformLigandStereochemistryOrganic ChemistryAntineoplastic AgentsDNATelomereLigandsG-quadruplexSettore CHIM/08 - Chimica FarmaceuticaBiochemistrySmall moleculeG-Quadruplexeschemistry.chemical_compoundOrder (biology)chemistrySettore CHIM/03 - Chimica Generale E InorganicaAnticancer drugs DNA G-quadruplex host-guest complexes ligand symmetry point group symmetryDrug DiscoveryMolecular symmetryHumansMolecular MedicineDNAStabilizer (chemistry)Current Medicinal Chemistry
researchProduct

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
researchProduct

Crystal structure of the coordination polymer [FeIII2{PtII(CN)4}3]

2015

[EN] The title complex, poly[dodeca--cyanido-diiron(III)triplatinum(II)], [FeIII2{PtII(CN)4}3], has a three-dimensional polymeric structure. It is built-up from square-planar [PtII(CN)4] 2 anions (point group symmetry 2/m) bridging cationic [FeIIIPtII(CN)4] + 1 layers extending in the bc plane. The FeII atoms of the layers are located on inversion centres and exhibit an octahedral coordination sphere defined by six N atoms of cyanide ligands, while the PtII atoms are located on twofold rotation axes and are surrounded by four C atoms of the cyanide ligands in a square-planar coordination. The geometrical preferences of the two cations for octahedral and square-planar coordination, respectiv…

Coordination sphereCoordination polymerStereochemistryCyanide02 engineering and technologyCrystal structure010402 general chemistry01 natural scienceschemistry.chemical_compoundSpin crossoverMolecular symmetryGeneral Materials ScienceSpin-crossoverCrystallographyCrystal structureCationic polymerizationGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsData Reports0104 chemical sciencesCrystallographychemistryQD901-999FISICA APLICADAPolycyanidometalate0210 nano-technologyActa Crystallographica Section E Crystallographic Communications
researchProduct

Organic Materials for Non-Linear Optics: The 2D Approach

1998

Conventional organic molecules for applications in second-order non-linear optics are donor–acceptor substituted π systems that show only one intense charge-transfer (CT) transition. Thus, only a single element of the second-order polarizability tensor, β, is significant in these one-dimensional systems. The advantages and optimization strategies for two new classes of molecules with multiple CT transitions and two-dimensional second-order polarizability are reviewed. These are donor–acceptor substituted π systems that lack a dipole and have a molecular symmetry of C3 or higher, and dipolar molecules of symmetry C2v. A basic introduction to the field is also given.

DipoleField (physics)ChemistryChemical physicsPolarizabilityMolecular symmetryMoleculeNonlinear opticsNanotechnologySingle elementGeneral MedicinePhysics::Chemical PhysicsSymmetry (physics)Journal f�r Praktische Chemie/Chemiker-Zeitung
researchProduct

Self-assembly, metal binding ability, and magnetic properties of dinickel(II) and dicobalt(II) triple mesocates

2012

Two metallacyclic complexes of general formula Na-8[(M2L3)-L-II]center dot xH(2)O [M = Ni (4) and Co (5) with x = 15 (4) and 17 (5)] have been self-assembled in aqueous solution from N,N'-1,3-phenylenebis(oxamic acid) (H4L) and M2+ ions in a ligand/metal molar ratio of 3 : 2 in the presence of NaOH acting as base. X-Ray structural analyses of 4 and 5 show triple-stranded, dinuclear anions of the meso-helicate-type (so-called mesocates) with C-3h molecular symmetry. The two octahedral metal-tris(oxamate) moieties of opposite chiralities (Delta, Lambda form) are connected by three m-phenylene spacers at intermetallic distances of 6.822(2) (4) and 6.868(2) angstrom (5) to give a metallacryptan…

Spin polarizationChemistryInorganic chemistryGeneral ChemistryCrystal structureCondensed Matter PhysicsMagnetic susceptibilityCrystallographyPhenyleneMolecular symmetryAntiferromagnetismMoleculeGeneral Materials ScienceMolecular orbital
researchProduct

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
researchProduct

Extension of the MIRS computer package for the modeling of molecular spectra : from effective to full ab initio ro-vibrational hamiltonians in irredu…

2012

The MIRS software for the modeling of ro-vibrational spectra of polyatomic molecules was considerably extended and improved. The original version (Nikitin, et al. JQSRT, 2003, pp. 239--249) was especially designed for separate or simultaneous treatments of complex band systems of polyatomic molecules. It was set up in the frame of effective polyad models by using algorithms based on advanced group theory algebra to take full account of symmetry properties. It has been successfully used for predictions and data fitting (positions and intensities) of numerous spectra of symmetric and spherical top molecules within the vibration extrapolation scheme. The new version offers more advanced possib…

ExtrapolationAb initioFOS: Physical sciences02 engineering and technologyPoint group01 natural scienceshigh-resolution infrared spectroscopyTheoretical physicsAb initio quantum chemistry methodsPhysics - Chemical PhysicsQuantum mechanics0103 physical sciencesMolecular symmetrypolyadsSpectroscopycomputational spectroscopyChemical Physics (physics.chem-ph)Physics[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Radiation010304 chemical physicsab initio calculationseffective hamiltoniansRotational–vibrational spectroscopy021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Opticsmolecular symmetryPhysics - Atmospheric and Oceanic Physicsvibration-rotation spectroscopy[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Atmospheric and Oceanic Physics (physics.ao-ph)Curve fittingirreducible tensors0210 nano-technologyGroup theory
researchProduct