Search results for " molecule"

showing 10 items of 1523 documents

Single Molecule Spectroscopy of Oriented Recombinant Trimeric Light Harvesting Complexes of Higher Plants

2002

The bleaching dynamics of reconstituted single light-harvesting chlorophyll a/b investigated. The complexes containing one histidine6 tag per monomeric subunit were immobilised predominantly in a defined orientation with their symmetry axis perpendicular to a Ni-ion-containing surface allowing for the first time the examination of single LHCIIb in an aqueous environment. Most complexes exhibit photobleaching in one step, indicating coupling between the monomeric subunits leading to an energy transfer between adjacent subunits. Differences in bleaching behaviour between these and previous observations with single LHCIIb are discussed.

Aqueous solutionProtein subunitClinical BiochemistryGeneral ChemistryPhotochemistryPhotobleachingGeneral Biochemistry Genetics and Molecular BiologySingle Molecule Spectroscopylaw.inventionLight-harvesting complexCoupling (electronics)chemistry.chemical_compoundCrystallographyMonomerchemistrylawRecombinant DNAMolecular BiologySingle Molecules
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Marine organisms as source of bioactive molecules applied in restoration projects

2015

Abstract In recent decades research in the conservation and restoration field has provided sustainable alternatives to traditional procedures for cleaning or controlling the microbial colonization of works of art. In the present study, for the first time novel bioactive molecules extracted from marine invertebrate organisms (Anthozoa) were tested instead of chemical compounds for removing protein layers or as a biocide for controlling fungal or bacterial colonization. In particular, Bioactive Molecules with Protease activity (BMP), acting in a temperature range of 4- 30°C, were tested for the hydrolysis of protein layers on laboratory specimens. The cleaning protocol provides a selective pr…

ArcheologyBiocideProteaseMarine invertebrate Biocleaning Protein layer Protease Antimicrobial peptides Biodegradation controlbiologymedicine.medical_treatmentMicrococcusBioactive moleculesConservationBacterial growthAspergillus sojaebiology.organism_classificationAntimicrobialMinimum inhibitory concentrationMarine organismPenicilliumSettore BIO/03 - Botanica Ambientale E ApplicatamedicineFood science
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Reorientations and translations in a fragile glass-former: magnetic resonance studies of meta-fluoroaniline

1999

Abstract The rotational dynamics in supercooled liquid and glassy meta-fluoroaniline was studied using proton and fluorine spin-lattice relaxation times. It is shown that while proton relaxation is dominated by homonuclear relaxation, for fluorine heteronuclear relaxation prevails. The results could be well described using a distribution of correlation times. The mean correlation times show pronounced deviations from the simple Arrhenius law. In addition translational self-diffusion coefficients were measured for T>200 K using a static magnetic field gradient technique.

Arrhenius equationCondensed matter physicsProtonChemistryOrganic ChemistrySpin–lattice relaxationMagnetostaticsHomonuclear moleculeAnalytical ChemistryInorganic ChemistrySpin–spin relaxationsymbols.namesakeHeteronuclear moleculesymbolsRelaxation (physics)SpectroscopyJournal of Molecular Structure
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Oxygen depletion in dense molecular clouds: a clue to a low O2 abundance?

2011

Context: Dark cloud chemical models usually predict large amounts of O2, often above observational limits. Aims: We investigate the reason for this discrepancy from a theoretical point of view, inspired by the studies of Jenkins and Whittet on oxygen depletion. Methods: We use the gas-grain code Nautilus with an up-to-date gas-phase network to study the sensitivity of the molecular oxygen abundance to the oxygen elemental abundance. We use the rate coefficient for the reaction O + OH at 10 K recommended by the KIDA (KInetic Database for Astrochemistry) experts. Results: The updates of rate coefficients and branching ratios of the reactions of our gas-phase chemical network, especially N + C…

AstrochemistryChemical models[SDU.ASTR.CO]Sciences of the Universe [physics]/Astrophysics [astro-ph]/Cosmology and Extra-Galactic Astrophysics [astro-ph.CO]Analytical chemistrychemistry.chemical_elementFOS: Physical sciencesAstrophysicsAstrophysicsKinetic energy01 natural sciencesOxygen[PHYS.ASTR.CO]Physics [physics]/Astrophysics [astro-ph]/Cosmology and Extra-Galactic Astrophysics [astro-ph.CO]0103 physical sciencesSolar and Stellar Astrophysics010303 astronomy & astrophysicsSolar and Stellar Astrophysics (astro-ph.SR)Astrophysics::Galaxy AstrophysicsPhysics010304 chemical physics[SDU.ASTR.SR]Sciences of the Universe [physics]/Astrophysics [astro-ph]/Solar and Stellar Astrophysics [astro-ph.SR]Molecular cloudAstronomy and Astrophysicsastrochemistry; ISM; abundances; ISM; molecules; ISM; individual objects; L134N; ISM; individual objects; TMC-1[PHYS.ASTR.SR]Physics [physics]/Astrophysics [astro-ph]/Solar and Stellar Astrophysics [astro-ph.SR]NitrogenchemistryAstrophysics - Solar and Stellar Astrophysics13. Climate actionSpace and Planetary ScienceMolecular oxygenChemical network
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The hyperfine structure in the rotational spectrum of CF+

2012

Context. CF+ has recently been detected in the Horsehead and Orion Bar photo-dissociation regions. The J=1-0 line in the Horsehead is double-peaked in contrast to other millimeter lines. The origin of this double-peak profile may be kinematic or spectroscopic. Aims. We investigate the effect of hyperfine interactions due to the fluorine nucleus in CF+ on the rotational transitions. Methods. We compute the fluorine spin rotation constant of CF+ using high-level quantum chemical methods and determine the relative positions and intensities of each hyperfine component. This information is used to fit the theoretical hyperfine components to the observed CF+ line profiles, thereby employing the h…

AstrochemistryFOS: Physical sciencesContext (language use)Astrophysics010402 general chemistryRotation01 natural sciencesISM: clouds0103 physical sciencesSpin (physics)010303 astronomy & astrophysicsHyperfine structureAstrophysics::Galaxy AstrophysicsLine (formation)PhysicsNebularadio lines: ISMastrochemistryAstronomy and AstrophysicsAstrophysics - Astrophysics of GalaxiesISM: molecules0104 chemical sciences[PHYS.ASTR.GA]Physics [physics]/Astrophysics [astro-ph]/Galactic Astrophysics [astro-ph.GA]Space and Planetary ScienceAstrophysics of Galaxies (astro-ph.GA)ISM: individual objects: Horsehead nebula[SDU.ASTR.GA]Sciences of the Universe [physics]/Astrophysics [astro-ph]/Galactic Astrophysics [astro-ph.GA]Atomic physicsBar (unit)
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Compact two-electron wave function for bond dissociation and Van der Waals interactions: A natural amplitude assessment

2014

Electron correlations in molecules can be divided in short range dynamical correlations, long range Van der Waals type interactions and near degeneracy static correlations. In this work we analyze for a one-dimensional model of a two-electron system how these three types of correlations can be incorporated in a simple wave function of restricted functional form consisting of an orbital product multiplied by a single correlation function $f(r_{12})$ depending on the interelectronic distance $r_{12}$. Since the three types of correlations mentioned lead to different signatures in terms of the natural orbital (NO) amplitudes in two-electron systems we make an analysis of the wave function in t…

Atomic Physics (physics.atom-ph)General Physics and AstronomyFOS: Physical sciencesPhysics - Atomic Physicssymbols.namesakeCondensed Matter - Strongly Correlated ElectronsAtomic orbitalQuantum mechanicsPhysics - Chemical PhysicsPhysics::Atomic PhysicsSDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryWave functionAnsatzPhysicsChemical Physics (physics.chem-ph)Quantum Physics/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyta114Electronic correlationStrongly Correlated Electrons (cond-mat.str-el)Computational Physics (physics.comp-ph)Diatomic molecule3. Good healthBond lengthAmplitudesymbolsvan der Waals forceQuantum Physics (quant-ph)Physics - Computational Physics
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Optical Shielding of Destructive Chemical Reactions between Ultracold Ground-State NaRb Molecules

2020

Polar quantum gases represent promising platforms for studying many-body physics and strongly correlated systems with possible applications e.g. in quantum simulation or quantum computation. Due to their large permanent electric dipole moment polar molecules in electric field exhibit strong long-range anisotropic dipole-dipole interactions (DDIs). The creation and trapping of ultracold dipolar diatomic molecules of various species are feasible in many experimental groups nowadays. However long time trapping is still a challenge even in the case of the so called nonreactive molecules which are supposed to be immune against inelastic collisions in their absolute ground state [1] . Various hyp…

Atomic Physics (physics.atom-ph)Inelastic collisionGeneral Physics and AstronomyFOS: Physical sciencesQuantum simulator01 natural sciences7. Clean energyMolecular physicslaw.inventionPhysics - Atomic Physics[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]law0103 physical sciencesMoleculeSpontaneous emissionPhysics::Atomic Physics010306 general physicsComputingMilieux_MISCELLANEOUSPhysics[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]Rotational–vibrational spectroscopyLaserDiatomic moleculeDipoleElectric dipole momentQuantum Gases (cond-mat.quant-gas)Excited stateAtom optics[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsCondensed Matter - Quantum GasesGround state
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Ab initio angle- and energy-resolved photoelectron spectroscopy with time-dependent density-functional theory

2012

We present a time-dependent density-functional method able to describe the photoelectron spectrum of atoms and molecules when excited by laser pulses. This computationally feasible scheme is based on a geometrical partitioning that efficiently gives access to photoelectron spectroscopy in time-dependent density-functional calculations. By using a geometrical approach, we provide a simple description of momentum-resolved photoemission including multiphoton effects. The approach is validated by comparison with results in the literature and exact calculations. Furthermore, we present numerical photoelectron angular distributions for randomly oriented nitrogen molecules in a short near-infrared…

Atomic Physics (physics.atom-ph)Photoemission spectroscopyAb initioFOS: Physical sciences02 engineering and technology01 natural sciences7. Clean energySpectral lineSettore FIS/03 - Fisica Della MateriaPhysics - Atomic PhysicsX-ray photoelectron spectroscopyTDDFTABOVE-THRESHOLD IONIZATION; LASER FIELDS; WAVE-FUNCTIONS; PHOTOEMISSION; CLUSTERS; SYSTEMS; PULSESMesoscale and Nanoscale Physics (cond-mat.mes-hall)0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersPhysics::Atomic Physics010306 general physicsPhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsAtoms in moleculesTime-dependent density functional theory021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics3. Good healthStrong field ionizationExcited stateDensity functional theoryAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)0210 nano-technology
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The role of Aurora-A inhibitors in cancer therapy

2007

Recently, new chemotherapy agents which target the non-structural components of mitosis have been developed. An important protein involved in several mitotic phases is the Aurora-A protein. By means of the phosphorylation of different substrates, Aurora-A regulates the correct development of the various phases of mitosis. The kinase activity of this protein makes Aurora-A an excellent candidate as an oncogene. The first data of Aurora-A involvement in cancer regarded the identification of Aurora-A overexpression in primary breast and colon tumour samples. With regard to the predictive role of Aurora-A, it has been shown that its overexpression disrupts the spindle checkpoint activated by pa…

Aurora inhibitorAntineoplastic Agentsmacromolecular substancesProtein Serine-Threonine KinasesBiologychemistry.chemical_compoundAurora kinaseAurora KinasesNeoplasmsAnimalsHumansKinase activityProtein Kinase InhibitorsMitosisHematologyCell biologyZM447439Aurora-A cancer treatment kinase inhibitor mitosis small moleculeenzymes and coenzymes (carbohydrates)Spindle checkpointNocodazoleOncologyAurora kinase inhibitor MK-0457chemistryembryonic structuresbiological phenomena cell phenomena and immunity
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The characterization of molecular alkaly metal azides

2006

Matrix isolation infrared (IR) studies have been carried out on the vaporisation of the alkali-metal azides MN(3) (M = Na, K, Rb and Cs). The results show that under high vacuum conditions, molecular KN(3), RbN(3) and CsN(3) are present as stable high-temperature vapour species, together with variable amounts of nitrogen gas and the corresponding metal atoms. The characterisation of these molecular azides is supported by ab initio molecular orbital calculations and density functional theory (DFT) calculations, and for CsN(3) in particular, by the detection of the isotopomers CS((14)N(15)N(14)N) and Cs((15)N(14)N(14)N). The IR spectra are assigned to a "side-on" (C(2v)) structure by comparis…

AzidesAlkali metalsInfraredChemistryOrganic ChemistryMatrix isolationAb initioAnalytical chemistryInfrared spectroscopyTheoretical calculationsGeneral ChemistryMatrix isolationCatalysisIsotopomersIR spectroscopyddc:540AtomCASSCF azides single moleculeDensity functional theoryMolecular orbital
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