Search results for "Spectral line"

showing 10 items of 1453 documents

Synthesis and Electronic Spectra of Substitutedp-Distyrylbenzenes for the Use in Light-Emitting Diodes

2000

The influence of substitution on the absorption and Luminescence spectra of oligo(phenylenevinylene)s has been studied using distyrylbenzene (DSB) as a model compound. The degree, character, and pattern of substitution was varied systematically, altering the electronic properties of the DSB, the wavelength of the emitted light could be tuned over a range of 100 nm. The syntheses of 6b—h were performed by twofold Wittig Horner-olefinations of bisphoshonates 1a, b with substituted benzaldehydes 2a—i, 6ivia Heck-reaction of the dibromosulfonylbenzene 3, 6k by Siegrist-reaction of 4 with N-phenylbenzaldimine and the Knoevenagel-reaction of benzyl cyanide with 5 led to 6l.

chemistry.chemical_compoundWavelengthUltraviolet visible spectroscopyChemistrylawWittig reactionBenzyl cyanideAbsorption (electromagnetic radiation)PhotochemistryFluorescence spectroscopySpectral lineLight-emitting diodelaw.inventionJournal für praktische Chemie
researchProduct

Comparison of the molecular structure and spectra of benzene and borazine

1970

Ab initio SCF MO and CI calculations for two different gaussian basis sets are carried out for the isoelectronic molecules benzene C6H6 and borazine B3N3H3 in order to investigate the effect of increasing the flexibility in the representation of their respective π systems. In the process it is found from comparison of orbital charge density contour diagrams and inner shell orbital energies of borazine with analogous data for other systems that the BN bonds of this compound are considerably less polar (B+N−) than that of ammonia borane BNH6 (B−N+). CI calculations employing the larger basis set produce generally better agreement with the experimental transition energies of benzene than do th…

chemistry.chemical_compoundchemistryBorazineAb initioCharge densityMoleculeChiropracticsPhysical and Theoretical ChemistryAtomic physicsBenzeneExcitationBasis setSpectral lineTheoretica Chimica Acta
researchProduct

Mass spectrometry of 3,4-dihydroquinazolin-4-ones of pharmaceutical interest. Part3. Electron ionization mass spectra of 2-substituted-3-(5′-pyrazoly…

1992

The fragmentation reactions induced by electron impact of eighteen title compounds has been investigated with the aid of low beam energy spectra (14 eV, nom. value), metastable ion detection, high resolution measurements and labelling experiments. The loss of the 4-carbonyl oxygen together with the 3-substituent, which constitutes a characteristic fragmentation route of 3-aryl and 3-heteroaromatic substituted-4(3H)-quinazolinones, is again observed, but the presence of a carboxyethyl group at the 4′-position of the pyrazole ring is responsible of an anomalous loss of 47 daltons from the molecular ion. Lastly, a comparison with the previously described behaviour of 3-(5′-isoxazolyl) derivati…

chemistry.chemical_compoundchemistryFragmentation (mass spectrometry)Organic ChemistryPolyatomic ionMass spectrumPhysical chemistryPyrazoleMass spectrometryElectron ionizationSpectral lineIonJournal of Heterocyclic Chemistry
researchProduct

Magneto-structural correlations and DFT calculations in two rare tetranuclear copper(II)-clusters with doubly phenoxo and end-on azido bridges: Synth…

2010

International audience; By slightly changing the synthetic conditions, we have prepared two closely related linear tetranuclear CuII complexes with the symmetrical ONNO donor tetradentate Schiff-base ligand [H2L = (OH)C6H4(CH3)Cdouble bond; length as m-dashN(CH2)3Ndouble bond; length as m-dashC(CH3)C6H4(OH)] and with azide ions. These two distinctly coloured crystalline products were characterized by elemental analysis, IR and UV–Vis spectroscopy, CV, EPR spectra and variable temperature magnetic measurements. Single crystal X-ray diffraction studies of the green [Cu4(μ-L)2(μ1,1-N3)2(N3)2] (1) and the red [Cu4(μ-L)2(μ1,1-N3)2(N3)2(H2O)2] (2) crystals show that the coordination environment o…

chemistry.chemical_elementCuII-tetranuclearDFT calculations010402 general chemistry01 natural sciencesSpectral lineIonlaw.inventionInorganic Chemistrychemistry.chemical_compoundlawMaterials Chemistry[CHIM]Chemical SciencesPhysical and Theoretical ChemistrySpectroscopyElectron paramagnetic resonanceLinear-clusters010405 organic chemistryMagnetic studyCopper0104 chemical sciencesCrystallographyMolecular geometrychemistryEPRAzideSingle crystalInorganica Chimica Acta
researchProduct

Conformational investigation of α,β‐dehydropeptides. XV: N‐acetyl‐α,β‐dehydroamino acid N ′N ′‐dimethylamides: conformational properties from infrare…

2005

The FTIR spectra were analysed in the region of the nu(s)(N-H), AI(C=O) and nu(s)(Calpha=Cbeta) bands for a series of Ac-DeltaXaa-NMe2, where DeltaXaa = DeltaAla, (Z)-DeltaAbu, (Z)-DeltaLeu, (Z)-DeltaPhe and DeltaVal, to determine a predominant solution conformation of these alpha,beta-dehydropeptide-related molecules. Measurements were taken in CCl4, DCM and MeCN solutions. In the same way, spectra of saturated analogues Ac-Xaa-NMe2, where Xaa = Ala, Abu, Leu, Phe and Val, were investigated. To help interpret the spectroscopic results, conformational maps were calculated by the B3LYP/6-31+G** method. Also, the relative energies of all conformers of the dehydro compounds in vacuo as well as…

conformationStereochemistryProtein ConformationαPeptideamide/π(Ph) interactionBiochemistrySpectral linechemistry.chemical_compoundStructural BiologyAmideDrug DiscoverySpectroscopy Fourier Transform InfraredSide chainMoleculeC5 hydrogen bondFourier transform infrared spectroscopysolute/solvent interactionMolecular BiologyConformational isomerismβ‐dehydroamino acidsPharmacologychemistry.chemical_classificationChemistryHydrogen bondOrganic ChemistryGeneral MedicineModels TheoreticalAmidestheoretical IR frequenciesFTIR spectroscopyMolecular Medicinedensity functional theory calculationsPeptidesJournal of Peptide Science
researchProduct

$PT$-symmetric graphene under a magnetic field

2016

We propose a $PT$-symmetrically deformed version of the graphene tight-binding model under a magnetic field. We analyze the structure of the spectra and the eigenvectors of the Hamiltonians around the $K$ and $K'$ points, both in the $PT$-symmetric and $PT$-broken regions. In particular we show that the presence of the deformation parameter $V$ produces several interesting consequences, including the asymmetry of the zero-energy states of the Hamiltonians and the breakdown of the completeness of the eigenvector sets. We also discuss the biorthogonality of the eigenvectors, which {turns out to be} different in the $PT$-symmetric and $PT$-broken regions.

deformed grapheneGeneral Mathematicsmedia_common.quotation_subjectMathematicsofComputing_GENERALStructure (category theory)General Physics and AstronomyFOS: Physical sciencesDeformation (meteorology)01 natural sciencesAsymmetrySpectral linelaw.inventionTheoretical physicslawCompleteness (order theory)0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)biorthogonal eigenstate010306 general physicsSettore MAT/07 - Fisica MatematicaEigenvalues and eigenvectorsResearch ArticlesMathematical Physicsmedia_commonPhysicsCondensed Matter - Mesoscale and Nanoscale Physics010308 nuclear & particles physicsGrapheneGeneral Engineering-symmetric HamiltonianMathematical Physics (math-ph)Magnetic field
researchProduct

High-resolution spectroscopy of difference and combination bands of SF6 to elucidate the ν3 + ν1 − ν1 and ν3 + ν2 − ν2 hot band structures in the ν3 …

2014

The strong infrared absorption in the ν3 S–F stretching region of sulphur hexafluoride (SF6) near 948 cm−1 makes it a powerful greenhouse gas. Although its present concentration in the atmosphere is very low, it is increasing rapidly, due to industrial pollution. The ground state population of this heavy species is only 32% at room temperature and thus many hot bands are present. Consequently, a reliable remote-sensing spectroscopic detection and monitoring of this species require an accurate modelling of these hot bands. We used two experimental set-ups at the SOLEIL French synchrotron facility to record some difference and combination bands of SF6: (1) a new cryogenic multiple pass cell w…

education.field_of_studyAbsorption spectroscopyChemistryPopulationBiophysicsAnalytical chemistryInfrared spectroscopyCondensed Matter PhysicsHot bandSpectral lineSynchrotronlaw.inventionlawPhysical and Theoretical ChemistrySpectroscopyeducationGround stateMolecular BiologyMolecular Physics
researchProduct

Comparative parallel characterization of particle populations with two mass spectrometric systems LAMPAS 2 and SPASS

2006

Abstract Two transportable laser mass spectrometers, Single Particle Analysis and Sizing System (SPASS) and Laser Mass Analyzer for Particles in the Airborne State (LAMPAS 2), have been applied to investigate the dependence of spectra patterns on instrumental parameters and data evaluation procedures in an inter-comparison experiment. Laboratory experiments showed the spectral response of both instruments for mineral particles before and after heterogeneous reactions. During a period of 47 h, both instruments determined size and chemical composition of several thousand single particles of an ambient particle population. Time-resolved evaluation (1-h resolution) of specific ion signals, whic…

education.field_of_studyChemistryPopulationAnalytical chemistrySingle particle analysisCondensed Matter PhysicsMass spectrometrySpectral lineAerosolParticleParticle sizePhysical and Theoretical ChemistryCluster analysisBiological systemeducationInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
researchProduct

Pyrene, a Test Case for Deep-Ultraviolet Molecular Photophysics

2019

We determined the complete relaxation dynamics of pyrene in ethanol from the second bright state, employing experimental and theoretical broadband heterodyne detected transient grating and two-dimensional photon echo (2DPE) spectroscopy, using pulses with duration of 6 fs and covering a spectral range spanning from 250 to 300 nm. Multiple lifetimes are assigned to conical intersections through a cascade of electronic states, eventually leading to a rapid population of the lowest long-living excited state and subsequent slow vibrational cooling. The lineshapes in the 2DPE spectra indicate that the efficiency of the population transfer depends on the kinetic energy deposited into modes requir…

education.field_of_studyMaterials sciencePhotonLetter010304 chemical physicsPopulationRelaxation (NMR)Conical intersection010402 general chemistryKinetic energy01 natural sciencesMolecular physicsSpectral line0104 chemical sciencespyrene 2D-UV computational spectroscopy computational photochemistryExcited state0103 physical sciencesGeneral Materials SciencePhysical and Theoretical ChemistryeducationSpectroscopy
researchProduct

Hartree-Fock calculations and photoelectron spectra of SSO and NSF

1974

Results from ab initio Hartree-Fock calculations on the ground states of SSO and NSF are reported. The calculations employ large basis sets of Gaussian functions of essentially double zeta quality. The photoelectron spectra of the bent triatomic molecules with 18 valence electrons, i.e. SSO, NSF, O3, SO2, NSCl are compared. Further experimental details of the photoelectron spectrum of SSO are presented and an assignment of the observed ionic states of SSO⊕ is attempted. The calculated dissociation energies, dipole moments and the population analyses are given. The correlation effect is qualitatively discussed in connection with the applicability of Koopmans' theorem for the bent tri-atomic …

education.field_of_studyPhotoemission spectroscopyChemistryTriatomic moleculePopulationAb initioHartree–Fock methodSpectral lineDipolePhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsChiropracticsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsValence electroneducationTheoretica Chimica Acta
researchProduct