Search results for "quantum theory"

showing 10 items of 234 documents

DFT studies of COOH tip-functionalized zigzag and armchair single wall carbon nanotubes

2011

Structure and energy calculations of pristine and COOH-modified model single wall carbon nanotubes (SWCNTs) of different length were performed at B3LYP/6-31G* level of theory. From 1 to 9 COOH groups were added at the end of the nanotube. The differences in structure and energetics of partially and fully functionalized SWCNTs at one end of the nanotube are observed. Up to nine COOH groups could be added at one end of (9,0) zigzag SWCNT in case of full functionalization. However, for (5,5) armchair SWCNT, the full functionalization was impossible due to steric crowding and rim deformation. The dependence of substituent attachment energy on the number of substituents at the carbon nanotube ri…

Steric effectsNanotubeMaterials scienceBiomedicine generalCarboxylic AcidsSubstituentHealth InformaticsCarbon nanotubeDFTCatalysislaw.inventionEnd-substitutionInorganic Chemistrychemistry.chemical_compoundCarboxylation energylawOrganic chemistryComputer SimulationComputer Applications in ChemistryPhysical and Theoretical ChemistryAnthracenesLife Sciences generalOriginal PaperNanotubes CarbonOrganic ChemistryZigzag and armchair SWCNTBenzoic AcidPhenanthrenesComputer Science ApplicationsChemistryCrystallographyModels ChemicalComputational Theory and MathematicschemistryZigzagComputer Appl. in Life SciencesQuantum TheoryThermodynamicsMolecular MedicineSurface modificationCOOH functionalization
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Hypoxia-Selective Dissociation Mechanism of a Nitroimidazole Nucleoside in a DNA Environment

2019

Photodynamic therapy is a promising approach to treat a variety of superficial tumors and other diseases. One of its major limitations arises from its dependence on molecular oxygen, which decreases the efficiency of the therapy in hypoxia conditions commonly developed by solid tumors. The present contribution reveals the molecular mechanism of a modified thymine bearing a nitroimidazole substituent, a photosensitizer able to produce highly harmful interstrand cross-links in the DNA double strand after irradiation selectively in absence of oxygen. The mechanism is resolved at a fully atomistic and electronic level relying on quantum mechanics (CASPT2, coupled-cluster, DFT, and TD-DFT method…

SubstituentMolecular Dynamics Simulation010402 general chemistry01 natural scienceschemistry.chemical_compoundMolecular dynamics[CHIM]Chemical SciencesGeneral Materials SciencePhotosensitizerA-DNAPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSPhotosensitizing AgentsNitroimidazole010405 organic chemistryHydrogen bondHydrogen BondingDNA0104 chemical sciencesThyminechemistryNitroimidazolesBiophysicsNucleic Acid ConformationQuantum TheoryDNAThe Journal of Physical Chemistry Letters
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A surface hopping algorithm for nonadiabatic minimum energy path calculations

2015

The article introduces a robust algorithm for the computation of minimum energy paths transiting along regions of near-to or degeneracy of adiabatic states. The method facilitates studies of excited state reactivity involving weakly avoided crossings and conical intersections. Based on the analysis of the change in the multiconfigurational wave function the algorithm takes the decision whether the optimization should continue following the same electronic state or switch to a different state. This algorithm helps to overcome convergence difficulties near degeneracies. The implementation in the MOLCAS quantum chemistry package is discussed. To demonstrate the utility of the proposed procedur…

Surface PropertiesComputationSurface hoppingCASSCFretinalHeterocyclic Compounds 1-RingHeterocyclic CompoundsasulamConvergence (routing)dioxetaneAdiabatic processWave functionSchiff BasesChemistrysurface hopping algorithmGeneral ChemistryKineticsComputational MathematicsExcited statePath (graph theory)RetinaldehydeQuantum TheoryThermodynamicsCarbamatesCASSCF; asulam; dioxetane; minimum energy path; retinal; surface hopping algorithm; thymineProtonsDegeneracy (mathematics)Algorithmminimum energy pathAlgorithmsThymineJournal of Computational Chemistry
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The mechanism of aquaporin inhibition by gold compounds elucidated by biophysical and computational methods

2017

The inhibition of water and glycerol permeation via human aquaglyceroporin-3 (AQP3) by gold(iii) complexes has been studied by stopped-flow spectroscopy and, for the first time, its mechanism has been described using molecular dynamics (MD), combined with density functional theory (DFT) and electrochemical studies. The obtained MD results showed that the most effective gold-based inhibitor, anchored to Cys40 in AQP3, is able to induce shrinkage of pores preventing glycerol and water permeation. Moreover, the good correlation between the affinity of the Au(iii) complex to Cys binding and AQP3 inhibition effects was highlighted, while no influence of the different oxidative character of the c…

Surfaces Coatings and FilmAquaporinCeramics and CompositeOxidative phosphorylationMolecular Dynamics Simulation010402 general chemistryElectrochemistry01 natural sciencesCatalysisCatalysiMolecular dynamicschemistry.chemical_compoundGold CompoundsJournal ArticleMaterials ChemistryGlycerolHumansOrganic chemistryAquaporin 3Molecular Structure010405 organic chemistryChemistryElectronic Optical and Magnetic MaterialChemistry (all)Metals and AlloysGeneral ChemistryPermeation0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSettore CHIM/03 - Chimica Generale E InorganicaCeramics and CompositesBiophysicsQuantum TheoryDensity functional theoryOrganogold CompoundsChemical Communications
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Electronic properties of graphene: A learning path for undergraduate students

2016

The purpose of this work is to present a learning path aimed at deepening student understanding of the fundamental concepts underlying the electronic properties of new materials, graphene in particular. To achieve this task, we propose a five-week long workshop where students may be introduced to fundamental concepts of advanced physics, rarely used in learning paths, such as the symmetry properties of the crystal lattice, the group theory , the features of the free electron wave functions and energy levels, the relativistic Dirac equation. Particular emphasis is given to the manner of introducing these concepts, since an essential knowledge of solid state physics, quantum physics and relat…

Theoretical computer scienceSolid-state physicsSettore FIS/08 - Didattica E Storia Della FisicaLattice theoryCrystal symmetryElectronSettore FIS/03 - Fisica Della MateriaTask (project management)EducationElectronic propertieRelativitysymbols.namesakeTheory of relativityMathematics educationLinear equationWave functionsPhysicsSequenceSymmetry (physics)Dirac equationQuantum theoryPath (graph theory)symbolsThe Conceptual FrameworkGroup theoryStudent
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New QM/MM implementation of the DFTB3 method in the gromacs package.

2015

The approximate density-functional tight-binding theory method DFTB3 has been implemented in the quantum mechanics/molecular mechanics (QM/MM) framework of the Gromacs molecular simulation package. We show that the efficient smooth particle–mesh Ewald implementation of Gromacs extends to the calculation of QM/MM electrostatic interactions. Further, we make use of the various free-energy functionalities provided by Gromacs and the PLUMED plugin. We exploit the versatility and performance of the current framework in three typical applications of QM/MM methods to solve biophysical problems: (i) ultrafast proton transfer in malonaldehyde, (ii) conformation of the alanine dipeptide, and (iii) el…

Theory methodComputer scienceMolecular simulationGeneral ChemistryExtended samplingFree energy simulationMolecular dynamicsDensity-functional tight-bindingComputational scienceQM/MMComputational MathematicsMolecular dynamicsQuantum TheoryThermodynamicsComputer Simulationta116Quantum mechanics/molecular mechanicsSoftwareProtein BindingJournal of computational chemistry
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An inconvenient influence of iridium(III) isomer on OLED efficiency.

2010

The recently reported heteroleptic cyclometallated iridium(III) complex [Ir(2-phenylpyridine)(2)(2-carboxy-4-dimethylaminopyridine)] N984 and its isomer N984b have been studied more in detail. While photo- and electrochemical properties are very similar, DFT/TDDFT calculations show that the two isomers have different HOMO orbital characteristics. As a consequence, solution processed OLEDs made using a mixture of N984 and isomer N984b similar to vacuum processed devices show that the isomer has a dramatic detrimental effect on the performances of the device. In addition, commonly used thermogravimetric analysis is not suitable for showing the isomerization process. The isomer could impact pe…

Thermogravimetric analysisInjectionMaterials scienceLightchemistry.chemical_elementTransportElectrochemistryPhotochemistryIridiumlaw.inventionPhosphorescent OledsInorganic ChemistryIsomerismComplexeslawOLEDElectrochemistryOrganometallic CompoundsDevicesIridiumDopantMolecular StructureConversionTime-dependent density functional theorychemistryElectrochemistry; Iridium; Isomerism; Molecular Structure; Organometallic Compounds; Light; Quantum TheoryGreenQuantum TheoryBipolar HostIsomerizationLight-emitting diodeLight-Emitting-Diodes
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DFT study on the cycloreversion of thietane radical cations.

2011

The molecular mechanism of the cycloreversion (CR) of thietane radical cations has been analyzed in detail at the UB3LYP/6-31G* level of theory. Results have shown that the process takes place via a stepwise mechanism leading to alkenes and thiobenzophenone; alternatively, formal [4 + 2] cycloadducts are obtained. Thus, the CR of radical cations 1a, b(center dot+) is initiated by C2-C3 bond breaking, giving common intermediates INa,b. At this stage, two reaction pathways are feasible involving ion molecule complexes IMCa,b (i) or radical cations 4a,b(center dot+) (ii). Calculations support that 1a(center dot+) follows reaction pathway (leading to the formal [4 + 2] cycloadducts 5a). By cont…

ThietaneSTEADY-STATEFree RadicalsStereoisomerismOXETANEOxetanePhotochemistryPolarizable continuum modelPHOTOINDUCED-ELECTRON-TRANSFERPhotoinduced electron transferchemistry.chemical_compoundQUIMICA ORGANICACICLOREVESIONCationsMolecule(THIA)PYRYLIUM SALTSSulfhydryl CompoundsPhysical and Theoretical ChemistryDNA PHOTOLYASEDFT CALCULATIONREPAIRMolecular StructureTHIETANECLEAVAGEOtras Ciencias QuímicasCiencias QuímicasStereoisomerismRADICAL CATIONchemistryRadical ionEXCITED-STATESPOLARIZABLE CONTINUUM MODELCyclizationDENSITYQuantum TheoryThiobenzophenoneCIENCIAS NATURALES Y EXACTASThe journal of physical chemistry. A
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Fluorescence Properties of the Chromophore-Binding Domain of Bacteriophytochrome from Deinococcus radiodurans

2013

Fluorescent proteins are versatile tools for molecular imaging. In this study, we report a detailed analysis of the absorption and fluorescence properties of the chromophore-binding domain from Deinococcus radiodurans and its D207H mutant. Using single photon counting and transient absorption techniques, the average excited state lifetime of both studied systems was about 370 ps. The D207H mutation slightly changed the excited state decay profile but did not have a considerable effect on the average decay time of the system or the shape of the absorption and emission spectra of the biliverdin chromophore. We confirmed that the fluorescence properties of both samples are very similar in vivo…

Time FactorsFluorescence in the life sciencesPhotochemistrychemistry.chemical_compoundBimolecular fluorescence complementationBacterial ProteinsEscherichia coliMaterials ChemistryPhysical and Theoretical Chemistryta116BiliverdinbiologyPhytochromeBiliverdineta1182Deinococcus radioduransChromophorebiology.organism_classificationFluorescenceRecombinant ProteinsProtein Structure TertiarySurfaces Coatings and FilmschemistryMutationQuantum TheorySpectrophotometry UltravioletDeinococcusBinding domainThe Journal of Physical Chemistry B
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Protein dynamics observed by tunable mid-IR quantum cascade lasers across the time range from 10 ns to 1 s

2017

We have developed a spectrometer based on tunable quantum cascade lasers (QCLs) for recording time-resolved absorption spectra of proteins in the mid-infrared range. We illustrate its performance by recording time-resolved difference spectra of bacteriorhodopsin in the carboxylic range (1800–1700 cm− 1) and on the CO rebinding reaction of myoglobin (1960–1840 cm− 1), at a spectral resolution of 1 cm− 1. The spectrometric setup covers the time range from 4 ns to nearly a second with a response time of 10–15 ns. Absorption changes as low as 1 × 10− 4 are detected in single-shot experiments at t > 1 μs, and of 5 × 10− 6 in kinetics obtained after averaging 100 shots. While previous time-res…

Time FactorsSpectrophotometry InfraredAbsorption spectroscopyAnalytical chemistry010402 general chemistry53001 natural sciencesMolecular physicsSpectral lineAnalytical Chemistrylaw.inventionchannelrhodopsinflash photolysislawSpectral resolutionAbsorption (electromagnetic radiation)InstrumentationSpectroscopyCarbon MonoxidebiologySpectrometerChemistrybacteriorhodopsinLasers010401 analytical chemistry500 Naturwissenschaften und Mathematik::530 Physik::530 PhysikWaterBacteriorhodopsinLasertime-resolved IR spectroscopyAtomic and Molecular Physics and Optics0104 chemical sciencesSolutionsKineticsCascadeBacteriorhodopsinsmyoglobinbiology.proteinQuantum Theory
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