Search results for "ddc:54"

showing 10 items of 218 documents

PyDSC: a simple tool to treat differential scanning calorimetry data

2020

AbstractHerein, we describe an open-source, Python-based, script to treat the output of differential scanning calorimetry (DSC) experiments, called pyDSC, available free of charge for download at https://github.com/leonardo-chiappisi/pyDSC under a GNU General Public License v3.0. The main aim of this program is to provide the community with a simple program to analyze raw DSC data. Key features include the correction from spurious signals, and, most importantly, the baseline is computed with a robust, physically consistent approach. We also show that the baseline correction routine implemented in the script is significantly more reproducible than different standard ones proposed by propriet…

Computer science030303 biophysicsDSC03 medical and health sciencesSoftwareDifferential scanning calorimetryprotein conformationPhysical and Theoretical ChemistrySpurious relationshipReliability (statistics)0303 health sciencesReproducibilityInstrument controlSIMPLE (military communications protocol)business.industry030302 biochemistry & molecular biologypolymer stabilityCondensed Matter PhysicsKey featuresbaseline correction540 Chemie und zugeordnete Wissenschaftenphase transitionddc:540businessAlgorithmPython
researchProduct

Peculiarities of the local structure in new medium- and high-entropy, low-symmetry tungstates

2022

G. Bakradze acknowledges financial support provided by the Latvian Council of Science for project no. 1.1.1.2/VIAA/3/19/444 (agreement no. 1.1.1.2/16/I/001) realized at the Institute of Solid State Physics, University of Latvia. The Institute of Solid State Physics, University of Latvia, as a centre of excellence, has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement no. 739508, project CAMART2.

Condensed Matter - Materials ScienceHigh-entropy oxidesMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences:NATURAL SCIENCES::Physics [Research Subject Categories]TungstatesGeneral ChemistryCondensed Matter Physics540ddc:540Reverse Monte Carlo methodGeneral Materials ScienceSolid solutionsExtended X-ray absorption fine structure
researchProduct

Ultrafast decay of the excited singlet states of thioxanthone by internal conversion and intersystem crossing.

2010

The experimental ultrafast photophysics of thioxanthone in several aprotic organic solvents at room temperature is presented, measured using femtosecond transient absorption together with high-level ab initio CASPT2 calculations of the singlet- and triplet-state manifolds in the gas phase, including computed state minima and conical intersections, transition energies, oscillator strengths, and spin-orbit coupling terms. The initially populated singlet pi pi* state is shown to decay through internal conversion and intersystem crossing processes via intermediate n pi* singlet and triplet states, respectively. Two easily accessible conical intersections explain the favorable internal conversio…

Conical intersectionsChemistryTransition statesQuantum yieldInternal conversion (chemistry)Atomic and Molecular Physics and OpticsPhotophysicsIntersystem crossingExcited stateddc:540Solvent effectsUltrafast laser spectroscopySinglet fissionAb initio calculationsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet stateChemphyschem : a European journal of chemical physics and physical chemistry
researchProduct

Kinetic control in the chiral recognition of three-bladed propellers

2010

The ion pair of the stereolabile C(3)-symmetric, i(+)o proton complex [1H](+) of diaza-macropentacycle 1 and the configurationally stable Delta-TRISPHAT ([Delta-3](-)) anion exists in the form of two diastereomers, namely, [Delta-(1.H)][Delta-3] and [Lambda-(1.H)][Delta-3], the ratio of which, in terms of diastereomeric excess (de) decreases in the order [D(8)]THF (28%)CD(2)Cl(2) (22%)CDCl(3) (20%)[D(8)]toluene (16%)C(6)D(6) (7%)[D(6)]acetone (0%) at thermodynamic equilibrium. Except in the case of [D(6)]acetone, the latter is reached after a period of time that increases from 1 h ([D(8)]THF) to 24 h (CDCl(3)). Moreover, the initial value of the de of [1.H][Delta-3] in CDCl(3), before the t…

CryptandsIon pairsProtonStereochemistryOrganic ChemistryKineticsDiastereomerProtonationGeneral ChemistryNuclear magnetic resonance spectroscopyTolueneCatalysischemistry.chemical_compoundCrystallographyKineticsDeprotonationchemistryddc:540Solvent effectsSolvent effectsHelical structures
researchProduct

Light-controlled reversible modulation of frontier molecular orbital energy levels in trifluoromethylated diarylethenes

2017

Among bistable photochromic molecules, diarylethenes (DAEs) possess the distinct feature that upon photoisomerization they undergo a large modulation of their π-electronic system, accompanied by a marked shift of the HOMO/LUMO energies and hence oxidation/reduction potentials. The electronic modulation can be utilized to remote-control charge- as well as energy-transfer processes and it can be transduced to functional entities adjacent to the DAE core, thereby regulating their properties. In order to exploit such photoswitchable systems it is important to precisely adjust the absolute position of their HOMO and LUMO levels and to maximize the extent of the photoinduced shifts of these energ…

Cyclic voltammetryBistabilityPhotoisomerizationQuantum yields010402 general chemistryPhotochemistryDiarylethene01 natural sciencesCatalysischemistry.chemical_compoundPhotochromismMoleculeMolecular orbitalHOMO/LUMOquantum yieldsFrontier molecular orbital energiesTrifluoromethyl010405 organic chemistryChemistryFrontier molecular orbital energieOrganic Chemistryfrontier molecular orbital energiesGeneral ChemistryphotochromismPhotochromismcyclic voltammetry0104 chemical sciencesdiarylethenes540 Chemie und zugeordnete WissenschaftenDiarylethenesddc:540IsomerizationChemistry - A European Journal
researchProduct

The electronic spectra of 2-(2′-hydroxybenzoyl)pyrrole and 2-(2′-methoxybenzoyl)pyrrole: a theoretical study

2005

The gas-phase electronic spectra of 2-(2 0 -hydroxybenzoyl)pyrrole and 2-(2 0 -methoxybenzoyl)pyrrole have been determined using multiconfigurational perturbation theory (CASPT2). Solvatochromic spectral shifts for these molecules have been measured in cyclohexane and methanol and the electrostatic components of these shifts have been estimated using the vertical electrostatic model (VEM 4.2) developed for the configuration interaction with single excitations model implemented with the intermediate neglect of differential overlap Hamiltonian (CIS/INDO/ S2). Comparison between theory and experiment and an interpretation of the main spectral differences between the two substituted pyrroles an…

CyclohexaneCASPT2benzoylpyrrolesolvatochromic shiftElectronic spectraSpectral linechemistry.chemical_compoundsymbols.namesakeComputational chemistryBenzoylpyrroleMoleculePhysical and Theoretical ChemistryCIS/INDO/S2PyrroleChemistryOrganic ChemistrySolvatochromismSolvationConfiguration interactionSolvatochromic shiftSettore CHIM/08 - Chimica Farmaceuticaelectronic spectraVEMddc:540symbolsHamiltonian (quantum mechanics)Journal of Physical Organic Chemistry
researchProduct

Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction.

2016

An NHC-catalyzed Michael/Michael/esterification domino reaction via homoenolate/enolate intermediates for the asymmetric synthesis of tetrasubstituted cyclopentanes is described.

CyclopentanesStereochemistry010402 general chemistry01 natural sciencesCatalysisDominoCatalysisStereocenterCascade reactiondomino reactionMaterials Chemistryta116cyclopentane motifs010405 organic chemistryChemistryMetals and AlloysEnantioselective synthesisGeneral Chemistry5400104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemistryddc:540Ceramics and CompositesChemical communications (Cambridge, England)
researchProduct

Enhanced β-turn conformational stability of tripeptides containing Δphe in cis over trans configuration

2013

Conformations of three pairs of dehydropeptides with the opposite configuration of the Delta Phe residue, Boc-Gly-Delta(Z/E)Phe-Phe-p-NA (Z- p -NA and E- p -NA), Boc-Gly-Delta(Z/E)Phe-Phe-OMe (Z-OMe and E-OMe), and Boc-Gly-Delta(Z/E)Phe-Phe-OH (Z-OH and E-OH) were compared on the basis of CD and NMR studies in MeOH, TFE, and DMSO. The CD results were used as the additional input data for the NMR-based calculations of the detailed solution conformations of the peptides. It was found that Z- p -NA, E- p -NA, Z-OMe, and Z-OH adopt the beta-turn conformations and E-OMe and E-OH are unordered. There are two overlapping type III beta-turns in Z- p -NA, type II' beta-turn in E- p -NA, and type II …

Dehydropeptide conformationCircular dichroismMagnetic Resonance SpectroscopyStereochemistryProtein ConformationPhenylalanineClinical BiochemistryTripeptideCircular dichroismTemperature coefficients of amide protonsBiochemistryNuclear magnetic resonancechemistry.chemical_compoundResidue (chemistry)Trans configurationchemistry [Oligopeptides]Amideotorhinolaryngologic diseasesHydrogen bondProtein StabilityDehydropeptidesCircular DichroismOrganic ChemistryStereoisomerismchemistryIntramolecular forceddc:540Dehydrophenylalanine configurationchemical synthesis [Oligopeptides]Conformational stabilitychemistry [Phenylalanine]OligopeptidesAmino Acids
researchProduct

Adsorption mechanism of arsenate by zirconyl-functionalized activated carbon

2007

Arsenate [As(V)] and arsenite [As(III)] sorption at the solid-water interface of activated carbon impregnated with zirconyl nitrate (Zr-AC) was investigated using X-ray absorption spectroscopy (XAS) and surface complexation modeling. The XAS data at the Zr K-edge suggest that the structure of the zirconyl nitrate coating is built from chains of edge-sharing ZrO8 trigonal dodecahedra bound to each other through two double hydroxyl bridges. The 8-fold coordination of each Zr atom is completed by four O atoms, which share a bit less than the two theoretically possible bidentate nitrate groups. On impregnation, two of the O atoms may lose their nitrate group and be transformed to hydroxyl group…

DenticityArsenitesSurface PropertiesInorganic chemistrychemistry.chemical_elementchemistry [Arsenites]Biomaterialschemistry.chemical_compoundColloid and Surface ChemistryAdsorptionOxidation statechemistry [Arsenates]medicineArsenicchemistry [Zirconium]ArseniteNitrateschemistry [Nitrates]Extended X-ray absorption fine structureSpectrum AnalysisX-Rayschemistry [Water]arsenic acidArsenateWaterCarbonchemistry [Carbon]Surfaces Coatings and FilmsElectronic Optical and Magnetic Materialsarsenitechemistryddc:540PotentiometryArsenatesAdsorptionZirconiumActivated carbonmedicine.drugJournal of Colloid and Interface Science
researchProduct

Determination of 129I/127I isotope ratios in liquid solutions and environmental soil samples by ICP-MS with hexapole collision cell

2003

The determination of I-129 in environmental samples at ultratrace levels is very difficult by ICP-MS due to a high noise caused by Xe impurities in argon plasma gas (interference of Xe-129(+)), possible (IH2+)-I-127 interference and an insufficient abundance ratio sensitivity of the ICP mass spectrometer for I-129/I-127 isotope ratio measurement. A sensitive, powerful and fast analytical technique for iodine isotope ratio measurements in aqueous solutions and contaminated soil samples directly without sample preparation using ICP-MS with a hexapole collision cell (ICP-CC-QMS) was developed. Oxygen is used as reaction and carrier gas for iodine thermal desorption via the gas phase from solid…

Detection limitArgonAnalytical chemistryThermal desorptionchemistry.chemical_elementMass spectrometryAnalytical ChemistryJchemistryImpurityDesorptionddc:540Sample preparationInductively coupled plasma mass spectrometrySpectroscopy
researchProduct