Search results for " Force"

showing 10 items of 2250 documents

Intramolecular electronic excitation energy transfer in donor∕acceptor dyads studied by time and frequency resolved single molecule spectroscopy

2008

Electronic excitation energy transfer has been studied by single molecule spectroscopy in donor/acceptor dyads composed of a perylenediimide donor and a terrylenediimide acceptor linked by oligo(phenylene) bridges of two different lengths. For the shorter bridge (three phenylene units) energy is transferred almost quantitatively from the donor to the acceptor, while for the longer bridge (seven phenylene units) energy transfer is less efficient as indicated by the occurrence of donor and acceptor emission. To determine energy transfer rates and efficiencies at the single molecule level, several methods have been employed. These comprise time-correlated single photon counting techniques at r…

AnthracenesTime FactorsLightMolecular StructurePhotochemistryChemistryTemperatureGeneral Physics and AstronomyElectronsP680ElectronImidesAcceptorMolecular electronic transitionSpectrometry FluorescenceEnergy TransferPhenyleneIntramolecular forceExcited statePolycyclic Aromatic HydrocarbonsPhysical and Theoretical ChemistryAtomic physicsPeryleneExcitationThe Journal of Chemical Physics
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Novel isoquinoline derivatives as antimicrobial agents.

2013

The wide variety of potent biological activities of natural and synthetic isoquinoline alkaloids encouraged us to develop novel antimicrobial isoquinoline compounds. We synthesized a variety of differently functionalized 1-pentyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolines (THIQs), including dihydroisoquinolinium salts (2 and 5), methyl pentanoate-THIQ (6), 1-pentanol-THIQ (7), ester derivatives (8-15) and carbamate derivatives (16-23). We employed classic intramolecular Bischler-Napieralski cyclodehydration to generate the isoquinoline core. All the structures were characterized by nuclear magnetic resonance and mass spectrometry. The bactericide and fungicide activities were evaluated f…

AntifungalCarbamateAntifungal Agentsmedicine.drug_classmedicine.medical_treatmentClinical BiochemistryPharmaceutical ScienceMicrobial Sensitivity TestsGram-Positive BacteriaBiochemistrychemistry.chemical_compoundStructure-Activity RelationshipAnti-Infective AgentsDrug DiscoveryGram-Negative BacteriamedicineOrganic chemistryStructure–activity relationshipIsoquinolineMolecular BiologyEster derivativesChemistryOrganic ChemistryFungiAntimicrobialIsoquinolinesAnti-Bacterial AgentsIntramolecular forceMolecular MedicineBioorganicmedicinal chemistry
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Structure of chloroantimonates(III) with an imidazolium cation: (C3H5N2)[SbCl4] and (C3H5N2)2[SbCl5]

2003

Abstract Two different chloroantimonates(III) with an imidazolium cation have been synthesized by the reaction of antimony trichloride and imidazole in an aqueous solution of hydrochloric acid. The crystals of (C3H5N2)[SbCl4] are monoclinic, space group C2/c, while (C3H5N2)2[SbCl5] crystallizes in the orthorhombic system, space group Pbcn. Both crystals are built of one dimensional zig-zag chains composed of [SbCl6]3− octahedra connected by edges and corners, respectively. The cavities between inorganic chains are filled by imidazolium cations. In both structures, one crystallographically independent imidazolium cation is rotationally disordered, and the positions of all atoms are split bet…

Antimony trichlorideHydrogen bondStereochemistryOrganic ChemistryIntermolecular forcedisorderAnalytical ChemistryInorganic ChemistryBond lengthCrystallographychemistry.chemical_compoundchloroantimonates(III)chemistryOctahedronoctahedral deformationhydrogen bondsImidazoleOrthorhombic crystal systemimidazolium cationSpectroscopyMonoclinic crystal systemJournal of Molecular Structure
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Correlation spectroscopy in molten and supercooled antimony trichloride.

1990

Correlation spectroscopy measurements performed on molten and supercooled antimony trichloride with the homodyne technique show correlation functions that have a nonexponential behavior. Two well-defined distributions of correlation times can be observed in different temporal regions. This behavior is discussed in terms of a structural relaxation of clusters dynamically formed by intermolecular and interchain bonds. The Arrhenius plot of these correlation times shows a linear behavior with the same activation energy for both. In contrast, the activation energy of shear viscosity has a different value, showing that the processes determining the temperature behavior of \ensuremath{\tau} and $…

Antimony trichloridePhysicsCondensed matter physicsIntermolecular forceRelaxation (NMR)ThermodynamicsActivation energyAtomic and Molecular Physics and OpticsArrhenius plotchemistry.chemical_compoundchemistryCorrelation functionSupercoolingEnergy (signal processing)Physical review. A, Atomic, molecular, and optical physics
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Sievietes militārajā dienestā: Dienējošu sieviešu pieredze vīriešu dominējošā vidē

2021

Militārā joma vēsturiski un sociāli tiek definēta kā tradicionāli vīrišķīga – tā ir, iespējams, viena no arhetipiski vīrišķīgākajām sociālajām struktūrām Rietumu sabiedrībā (Segal 1995). Taču militārajā dienestā un karadarbībā tik un tā sastopamas arī sievietes. Šajā bakalaura darbā pētīta 23 sieviešu pieredze, kuras visas dienē vai dienējušas Kanādas Bruņotajos spēkos (KBS) pēdējo četrdesmit gadu laikā. Šo sieviešu pieredze apkopota daļēji strukturētās intervijās, kas veiktas gan klātienē, gan rakstiskā formātā. Izmantojot Pjēra Burdjē teoriju par maskulīno dominanci un Reivinas Konelas koncepciju par maskulīno hegemoniju, darbā esmu pētījusi, kā sievietes pieredz militāro vidi caur dzimtē…

AntropoloģijaCanadian Armed ForcesFemale soldiersHegemonic masculinityGendered discrimination
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Resonance frequency analysis after the placement of 133 dental implants

2006

Introducción: La estabilidad primaria del implante dental está relacionada con el hueso que se encuentra en contacto con él y se puede medir mediante el análisis de frecuencia de resonancia. Material y métodos: En 133 implantes (62 en maxilar y 71 en mandíbula) se midió la frecuencia de resonancia y la fuerza de inserción para conocer la estabilidad de los implantes el día de la cirugía, y estudiar su relación con distintas variables. Resultados: El cociente de estabilidad del implante obtenido el día de la cirugía fue de 62’1 y el de la fuerza de inserción fue de 35’7 Nw. La fuerza de inserción fue proporcional al análisis de la frecuencia de resonancia, a mayor fuerza de inserción mayor c…

Análisis de la frecuencia de resonancia (AFR)insertion force (IF)implantes dentalesdental implantsimplant stability quotient (ISQ)UNESCO::CIENCIAS MÉDICASfuerza de inserción (FI):CIENCIAS MÉDICAS [UNESCO]cociente de estabilidad del implante (valor ISQ)Resonance frequency analysis (RFA)
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Energetic coupling between plastids and mitochondria drives CO2 assimilation in diatoms.

2015

International audience; Diatoms are one of the most ecologically successful classes of photosynthetic marine eukaryotes in the contemporary oceans. Over the past 30 million years, they have helped to moderate Earth's climate by absorbing carbon dioxide from the atmosphere, sequestering it via the biological carbon pump and ultimately burying organic carbon in the lithosphere. The proportion of planetary primary production by diatoms in the modern oceans is roughly equivalent to that of terrestrial rainforests. In photosynthesis, the efficient conversion of carbon dioxide into organic matter requires a tight control of the ATP/NADPH ratio which, in other photosynthetic organisms, relies prin…

Aquatic Organismschemistry.chemical_compoundAdenosine TriphosphateSettore BIO/04 - Fisiologia VegetaleCYCLIC ELECTRON FLOWPlastidsPhotosynthesisPHAEODACTYLUM-TRICORNUTUMPlant Proteinschemistry.chemical_classificationMultidisciplinarymicroalgaeRespirationCarbon fixationEnergetic interactionsProton-Motive ForceMitochondriametabolic mutantPhenotypeATP/NADPH ratioOXYGEN PHOTOREDUCTIONCarbon dioxideOxidoreductasesOxidation-ReductionOceanOceans and SeasElectron flowMarine eukaryotesBiologyPhotosynthesisCHLAMYDOMONAS-REINHARDTIICarbon cycleCarbon CycleMitochondrial ProteinsEnergetic exchangesBotanyOrganic matterEcosystem[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology14. Life underwaterPlastidEcosystemDiatomsChemiosmosisfungiECSCarbon Dioxidechemistry13. Climate actionNADP
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Towards the understanding at the molecular level of the structured-water absorption and fluorescence spectra: a fingerprint of π-stacked water

2013

An intriguing absorption peak around ∼270 nm (4.59 eV) has been recurrently recorded in aqueous solutions of salts, sugars, amino acids, in the free-solute zone (exclusion zone) adjacent to various hydrophilic surfaces, as well as a transient in the conversion process of ice to water. The corresponding associated fluorescence has been observed in the interval 480–490 nm (2.58–2.53 eV). The spectroscopic features have been related to the presence of structured water but its nature remains incompletely understood. On the basis of high-level ab initio computations, the main absorption feature of structured water is assigned to the presence of two π-stacked ground-state water molecules, prefera…

Aqueous solutionAbsorption spectroscopyChemistryDimerBinding energyIntermolecular forceBiophysicsAnalytical chemistryCondensed Matter Physicschemistry.chemical_compoundExcited stateSinglet statePhysical and Theoretical ChemistryAbsorption (chemistry)Molecular BiologyMolecular Physics
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Polychromatic femtosecond fluorescence studies of metal–polypyridine complexes in solution

2011

Femtosecond-resolved broadband fluorescence studies are reported for[ M(bpy)(3)](2+) (M = Fe, Ru), RuN3 and RuN719 complexes in solution. We investigated the pump wavelength dependence of the fluorescence of aqueous [ Fe(bpy)(3)](2+) and the solvent and ligand dependence of the fluorescence of Ru-complexes excited at 400 nm. For all complexes, the (MLCT)-M-1 fluorescence appears at zero time delay with a mirror-like image with respect to the absorption. It decays in <= 30-45 fs due to intersystem crossing to the (MLCT)-M-3 states, but a longer lived component of similar to 190 fs additionally shows up in RuN719 and RuN3. No solvent effects are detected. The very early dynamics are character…

Aqueous solutionChemistryFluorescence up-conversionSettore FIS/01 - Fisica SperimentaleGeneral Physics and AstronomyIntersystem crossingMetal–polypyridine complexes; IVR; Internal conversion; Intersystem crossing; Ultrafast; Fluorescence up-conversionPhotochemistryFluorescencePhotoinduced electron transferIntersystem crossingInternal conversionUltrafastExcited stateIntramolecular forceFemtosecondIVRMetal–polypyridine complexePhysical and Theoretical ChemistrySolvent effects
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A quantum mechanics-molecular mechanics study of dissociative electron transfer : The methylchloride radical anion in aqueous solution

2002

The dissociative electron transfer reaction CH3Cl+e−→CH3•+Cl− in aqueous solution is studied by using a QM/MM method. In this work the quantum subsystem (a methylchloride molecule plus an electron) is described using density functional theory while the solvent (300 water molecules) is described using the TIP3P classical potential. By means of molecular dynamics simulations and the thermodynamic integration technique we obtained the potential of mean force (PMF) for the carbon–chlorine bond dissociation of the neutral and radical anion species. Combining these two free energy curves we found a quadratic dependence of the activation free energy on the reaction free energy in agreement with Ma…

Aqueous solutionChemistryGeneral Physics and AstronomyThermodynamic integrationFree radicalsMolecular dynamics methodOrganic compounds ; Dissociation ; Charge exchange ;Free radicals ; Negative ions ; Molecular dynamics method ; Digital simulationKinetic energyNegative ionsUNESCO::FÍSICA::Química físicaMolecular dynamicsElectron transferQuantum mechanicsOrganic compoundsMoleculeDensity functional theoryPhysical and Theoretical ChemistryPotential of mean forcePhysics::Chemical PhysicsCharge exchangeDigital simulation:FÍSICA::Química física [UNESCO]Dissociation
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