Search results for "METASTABILITY"

showing 10 items of 262 documents

A new improved synthesis of the 110 K bismuth superconducting phase: freeze-drying of acetic solutions

1992

Abstract Metastability has greatly hindered the separated synthesis of the high-temperature superconducting phases represented as (Bi1−x, Pbx)2Sr2Can−1CunO4 + 2n (n = 2, 2-2-1-2, Tc≈80 K, and n = 3, 2-2-2-3, Tc≈110 K). By careful control of the synthetic variables, it becomes possible to obtain the 110 K phase as the only superconducting one through processing of freeze-dried acetic solutions. This technique leads to homogeneously sized (5–10 μm) micaceous platelets of the superconducting material.

chemistry.chemical_classificationSuperconductivityAqueous solutionMaterials scienceMechanical EngineeringInorganic chemistryAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsBismuthchemistryMechanics of MaterialsPhase (matter)MetastabilityGeneral Materials ScienceInorganic compoundStoichiometrySolid solutionMaterials Letters
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Inside Back Cover: N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates (Ange…

2020

chemistry.chemical_compoundCrystallographyMaterials sciencechemistryMetastabilitySupramolecular chemistryCover (algebra)General ChemistryJ-aggregateCatalysisPeryleneAngewandte Chemie International Edition
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Innenrücktitelbild: N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates (Ang…

2020

chemistry.chemical_compoundCrystallographychemistryMetastabilitySupramolecular chemistryGeneral MedicinePeryleneAngewandte Chemie
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Differentiation of isomeric cyclic diamides by electron impact mass spectra

1976

The behaviour under electron impact of two series of isomeric cyclopentane- and cyclohexane-1, 2- and -1, 3-dicarboxylic acid dipiperidides was studied. Diagnostic fragmentation pathways were found to differentiate the isomeric diamides. Additional evidence was obtained from the metastable transitions.

chemistry.chemical_compoundFragmentation (mass spectrometry)chemistryComputational chemistryMetastabilityMass spectrumAnalytical chemistryMolecular MedicineCyclopentaneInstrumentationBiochemistrySpectroscopyElectron ionizationOrganic Mass Spectrometry
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Solubility-Driven Isolation of a Metastable Nonagold Cluster with Body-Centered Cubic Structure.

2020

The conventional synthetic methodology of atomically precise gold nanoclusters using reduction in solutions offers only thermodynamically most stable nanoclusters. We report herein a solubility‐driven isolation strategy to access the synthesis of a metastable gold cluster. The cluster, with the composition of [Au 9 (PPh 3 ) 8 ] + ( 1 ), displays an unusual, nearly perfect body‐centered‐cubic (bcc) structure. As revealed by ESI‐MS and UV/Vis measurement, the cluster is metastable in solution and converts to the well‐known [Au 11 (PPh 3 ) 8 Cl 2 ] + ( 2 ) within just 90 min. DFT calculations revealed that while both 1 and 2 are eight‐electron superatoms, there is a driving force to convert 1 …

cluster transformationBand gapnanoclusterCubic crystal system010402 general chemistry01 natural sciencesCatalysiskultaNanoclusterslaw.inventionMetalklusteritlawMetastabilityCluster (physics)metastable compoundsAu9CrystallizationGold cluster010405 organic chemistryChemistryOrganic ChemistryGeneral Chemistrygold0104 chemical sciencesCrystallographyvisual_artvisual_art.visual_art_mediumnanohiukkasetChemistry (Weinheim an der Bergstrasse, Germany)
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The [Fe(etz)6](BF4)2 Spin-Crossover System—Part One: High-Spin ⇌ Low-Spin Transition in Two Lattice Sites

1996

The [Fe(etz),](BF,), spin-cross-over system (etz = 1-ethyl-1 H-tetrazole) crystallizes in space group P1, with the following lattice constants at 298 K: a 10.419(3), b=15.709(1), c = 18.890(2) A = = 71.223(9), =77.986(10), and = 84.62(1)° V = 2862.0(9) A3 and Z = 3. Two nonequivalent lattice sites, one without (site A) and one with (site B) inversion symmetry, are observed. The population of the two sites nA:nB is 2:l. Iron(II) on site A undergoes a thermal low-spin (LS) high-spin (HS) transition with T1/2I, = 105 K. whereas that on site B remains in the high-spin state down to cryogenic temperatures. Application of external pressure of up to 1200 bar between 200 and 60 K does not cause for…

education.field_of_studyChemistryOrganic ChemistryPopulationPoint reflectionSpin transitionGeneral ChemistryCatalysisExternal pressureCrystallographyNuclear magnetic resonanceLattice constantSpin crossoverMetastabilityLattice (order)educationChemistry - A European Journal
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Lifetime measurements of the 3D3/2 and 3D5/2 metastable states in CaII

1993

The lifetime of the metastable 3D3/2 and 3D5/2 states of Ca+ ions is determined in a r.f. ion trap by laser excitation of this levels and subsequent time delayed probing of the state population by a second laser. In a buffer gas atmosphere of about 10−5−10−6 mbar of He we observe quenching to the ground state and strong finestructure mixing of the two D-states. This mixing allowes only the determination of the combined lifetime. Our result of τ(3D)=1.24(39) s is in good agreement with theoretical calculations.

education.field_of_studyMaterials scienceBuffer gasPopulationLaserAtomic and Molecular Physics and OpticsIonlaw.inventionlawExcited stateMetastabilityIon trapAtomic physicsGround stateeducationZeitschrift f�r Physik D Atoms, Molecules and Clusters
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Energy transfer in diiodoBodipy-grafted upconversion nanohybrids.

2015

Steady-state and time-resolved emission studies on nanohybrids consisting of NaYF4:Yb,Er and a diiodo-substituted Bodipy (UCNP-IBDP) show that the Yb(3+) metastable state, formed after absorption of a near-infrared (NIR) photon, can decay via two competitive energy transfer processes: sensitization of IBDP after absorption of a second NIR photon and population of Er(3+) excited states.

education.field_of_studyPhotonMaterials scienceEnergy transferPopulationPhysics::OpticsNanotechnologyAstrophysics::Cosmology and Extragalactic Astrophysics02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesPhoton upconversion0104 chemical scienceschemistry.chemical_compoundchemistryExcited stateMetastabilityGeneral Materials ScienceBODIPY0210 nano-technologyAbsorption (electromagnetic radiation)educationAstrophysics::Galaxy AstrophysicsNanoscale
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Equilibrium fluid-crystal interfacial free energy of bcc-crystallizing aqueous suspensions of polydisperse charged spheres

2015

The interfacial free energy is a central quantity in crystallization from the meta-stable melt. In suspensions of charged colloidal spheres, nucleation and growth kinetics can be accurately measured from optical experiments. In previous work, from this data effective non-equilibrium values for the interfacial free energy between the emerging bcc-nuclei and the adjacent melt in dependence on the chemical potential difference between melt phase and crystal phase were derived using classical nucleation theory. A strictly linear increase of the interfacial free energy was observed as a function of increased meta-stability. Here, we further analyze this data for five aqueous suspensions of charg…

fluid-crystalMaterials scienceNucleationFOS: Physical sciencesThermodynamicsNon-equilibrium thermodynamicsCondensed Matter - Soft Condensed Matter01 natural scienceslaw.inventionColloidlawMetastability0103 physical sciencesCrystallization010306 general physicsCondensed Matter - Statistical MechanicsCondensed Matter - Materials ScienceAqueous solutionStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsMaterials Science (cond-mat.mtrl-sci)Condensed Matter::Soft Condensed Matterpolydisperseinterfacial free energySoft Condensed Matter (cond-mat.soft)SPHERESClassical nucleation theoryPhysical Review E
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Triggering a transient organo-gelation system in a chemically active solvent

2021

A transient organo-gelation system with spatiotemporal dynamic properties is described. Here, the solvent actively controls a complex set of equilibria that underpin the dynamic assembly event. The observed metastability is due to the in situ formation of a secondary solvent, acting as an antagonist against the primary solvent of the organogel. peerReviewed

geelitPhysics::Biological PhysicsQuantitative Biology::BiomoleculesChemistryEvent (relativity)Metals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventliukeneminenCondensed Matter::Soft Condensed MatterChemical physicstermodynamiikkaMetastabilityMaterials ChemistryCeramics and CompositesTransient (oscillation)Physics::Chemical Physicsorgaaniset yhdisteet
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