Search results for "BIC"

showing 10 items of 4569 documents

Atomic structure of manganese-doped yttrium orthoaluminate

2018

Abstract Using hybrid exchange-correlation functional within density functional theory we have performed first-principle total energy calculations of Mn-doped yttrium orthoaluminate (YAlO3). Its equilibrium atomic structure has been predicted through optimization of coordinates of all atoms using a supercell approach. In our research both Mn3+ and Mn2+ ions have been substituted for the host alumina atom at orthorhombic Pbnm unit cell of YAlO3. F-center has been implemented as charge-compensating defect in case, when Mn2+ dopant is under study. In this study we thoroughly analyze the atomic displacements in seven nearest to Mn ion coordination spheres. Insertion of isoelectronic substitutio…

010302 applied physicsNuclear and High Energy PhysicsMaterials scienceCoordination sphereDopantchemistry.chemical_element02 engineering and technologyYttrium021001 nanoscience & nanotechnology01 natural sciencesCrystallographic defectCrystallographychemistryOctahedron0103 physical sciencesAtomOrthorhombic crystal systemDensity functional theory0210 nano-technologyInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Marginal and internal fit evaluation of conventional metal-ceramic versus zirconia CAD/CAM crowns

2019

Background The purpose of this in vivo study was to compare the marginal and internal gap widths of monolithic zirconia crowns fabricated by CAD/CAM technique and metal-ceramic crowns fabricated by conventional technique. Material and methods 10 participants needing a single restoration were selected. Zirconia crowns using CAD/CAM technology (Group A) (n=10) and metal-ceramic crowns (Group B) (n=10) using lost wax casting technique were fabricated for each selected tooth. The marginal and internal gaps of crowns were recorded using a replica technique with light body silicone material stabilized with a regular set putty. Each replica was sectioned buccolingually and mesiodistally and then e…

010302 applied physicsOrthodonticsProsthetic DentistryMaterials scienceResearchMonolithic zirconiaCAD02 engineering and technology:CIENCIAS MÉDICAS [UNESCO]021001 nanoscience & nanotechnology01 natural sciencesMetal ceramicPaired samplesUNESCO::CIENCIAS MÉDICAS0103 physical sciencesStereo microscopeCubic zirconia0210 nano-technologyGeneral DentistryConventional techniqueJournal of Clinical and Experimental Dentistry
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Relaxation of polarization in (K0.5Na0.5)(Nb0.93Sb0.07)O3 ferroelectric ceramics modified by BaTiO3

2017

ABSTRACTA study of low-frequency relaxation of polarization in conventionally prepared ceramic compounds of (1-x)(K0.5Na0.5)(Nb0.93Sb0.07)O3+xBaTiO3+0.5mol.%MnO2 (x = 0.02, 0.04) examined over a wide temperature range is reported. Anomalous behavior of the temperature dependence of the coercive field Ec(T) is detected in the temperature range of the orthorhombic to tetragonal phase transition. The observed features of polarization are assigned to dynamics of the domain structure at the temperature range of phase coexistence.

010302 applied physicsPhase transitionMaterials scienceCondensed matter physicsFerroelectric ceramics02 engineering and technologyCoercivityAtmospheric temperature range021001 nanoscience & nanotechnologyCondensed Matter PhysicsPolarization (waves)01 natural sciencesElectronic Optical and Magnetic MaterialsTetragonal crystal systemNuclear magnetic resonancevisual_art0103 physical sciencesvisual_art.visual_art_mediumOrthorhombic crystal systemCeramic0210 nano-technologyFerroelectrics
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Formation of translucent nanostructured zirconia ceramics

2021

Abstract In this work the mechanisms that affect the optical transparency of nanostructured translucent ZrO2 ceramics are studied. The translucent ceramic samples were obtained from a low agglomeration nanosized powder at low pressure and low temperature sintering. Even low pressures cause structural changes and defect creation in the nanocrystals. Annealing was used to study the grain formation, structure and impact of defects. Significant changes in translucency were observed with increase in pore size. In order to further understand the defect creation, the obtained ceramics were doped with Er3+ ions and studied optically. Photoluminescence studies revealed a change in the ratio of green…

010302 applied physicsQuenchingMaterials sciencePhotoluminescenceScanning electron microscopeAnnealing (metallurgy)Sintering02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesChemical engineeringTransmission electron microscopyvisual_art0103 physical sciencesMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumCubic zirconiasense organsCeramic0210 nano-technologyJournal of the European Ceramic Society
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Crystallographic snapshots of host–guest interactions in drugs@metal–organic frameworks: towards mimicking molecular recognition processes

2018

We report a novel metal–organic framework (MOF) featuring functional pores decorated with hydroxyl groups derived from the natural amino acid L-serine, which is able to establish specific interactions of different natures, strengths and directionalities with organic molecules of technological interest, i.e. ascorbic acid, pyridoxine, bupropion and 17-β-estradiol, based on their different sizes and chemical natures. The ability of 1 to distinctly organize guest molecules within its channels, through the concomitant effect of different directing supramolecular host–guest interactions, enables gaining unique insights, by means of single-crystal X-ray crystallography, into the host–guest intera…

010405 organic chemistryChemistryProcess Chemistry and TechnologySupramolecular chemistrymacromolecular substances010402 general chemistryAscorbic acid01 natural sciences0104 chemical sciencesOrganic moleculesCrystallographyMolecular recognitionMechanics of MaterialsMoleculeGeneral Materials ScienceMetal-organic frameworkElectrical and Electronic EngineeringMaterials Horizons
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Chiral and Racemic Spin Crossover Polymorphs in a Family of Mononuclear Iron(II) Compounds

2017

[EN] Understanding the origin of cooperativity and the equilibrium temperature of transition (T1/2) displayed by the spin-crossover (SCO) compounds as well as controlling these parameters are of paramount importance for future applications. For this task, the occurrence of polymorphism, presented by a number of SCO complexes, may provide deep insight into the influence of the supramolecular organization on the SCO behavior. In this context, herein we present a novel family of mononuclear octahedral FeII complexes with formula cis- [Fe(bqen)(NCX)2], where bqen is the chelating tetradentate ligand N,N¿-bis(8-quinolyl)ethane-1,2-diamine and X = S, Se. Depending on the preparation method, these…

010405 organic chemistryChemistryStereochemistrySupramolecular chemistryCooperativity010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographyOctahedronPolymorphism (materials science)Spin crossoverFISICA APLICADARacemic mixtureOrthorhombic crystal systemPhysical and Theoretical ChemistryEnantiomerInorganic Chemistry
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From self-inclusion and host-guest complexes to channel structures

2012

Various supramolecular interactions are applied as driving forces in self-assembly and molecular recognition processes. Single crystal X-ray diffraction method is especially important for solid-state studies of non-covalent interactions as it reveals their influence on the molecular and supramolecular structures. This paper discusses structures of two completely different types of compounds in which a variety of intermolecular interactions are involved. It will be shown that strong and weak intermolecular hydrogen bonds in N-alkylammonium resorcinarene salts, depending on the type of anion, inclusion of resorcinarene upper rim pendant group or solvent molecules into the cavity, strongly aff…

010405 organic chemistryChemistryStereochemistryX-ray structure; supramolecular chemistry; hydrogen bonding; hydrophobic interaction; resorcinarene; palladium complexSupramolecular chemistryGeneral ChemistryInclusion (mineral)010402 general chemistryta11601 natural sciencesHost (network)0104 chemical sciencesCommunication channel
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Stepwise Construction of Heterobimetallic Cages by an Extended Molecular Library Approach.

2017

Two novel heterobimetallic complexes, a trigonal-bipyramidal and a cubic one, have been synthesized and characterized using the same C3-symmetric metalloligand, prepared by a simple subcomponent self-assembly strategy. Adopting the molecular library approach, we chose a mononuclear, preorganized iron(II) complex as the metalloligand capable of self-assembly into a trigonal-bipyramidal or a cubic aggregate upon coordination to cis-protected C2-symmetric palladium(II) or unprotected tetravalent palladium(II) ions, respectively. The trigonal-bipyramidal complex was characterized by NMR and UV–vis spectroscopy, electrospray ionization mass spectrometry (ESI-MS), and single-crystal X-ray diffrac…

010405 organic chemistryChemistrytrigonal-bipyramidal and cubic heterobimetallic cagesElectrospray ionizationchemistry.chemical_element010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesIonInorganic ChemistryCrystallographyPhysical and Theoretical ChemistrySpectroscopyta116extended molecular library approachPalladiumInorganic chemistry
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Enhancement of the Intermolecular Magnetic Exchange through Halogen···Halogen interactions in Bisadeninium Rhenium(IV) Salts

2017

Two novel ReIV salts of general formula [H2ade]2[ReIVX6]X2·4H2O [H2ade2+ = 9H-adenine-1,7-diium; X = Cl(1) and Br(2)] have been synthesized and magneto-structurally characterized. 1 and 2 are isostructural salts that crystallize in the orthorhombic system with space group Fdd2. Both compounds are made up of discrete mononuclear [ReIVX6]2- and X- anions and doubly protonated adenine cations. The six-coordinate rhenium(IV) ion is bonded to six halide ligands [X = Cl (1) and Br (2)] in an octahedral geometry. Short intermolecular ReIV−X···X−ReIV interactions, as well as ReIV−X···H−N(H2ade) and ReIV−X···H−Ow hydrogen bonds, are present in the crystal lattice of 1 and 2. Magnetic suscep-tibility…

010405 organic chemistryInorganic chemistryIntermolecular forcechemistry.chemical_elementGeneral ChemistryCrystal structureRhenium010402 general chemistryCondensed Matter Physics01 natural sciencesMagnetic susceptibility0104 chemical sciencesCrystallographychemistryOctahedral molecular geometryHalogenGeneral Materials ScienceOrthorhombic crystal systemIsostructural
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A novel comprehensive procedure for estimating greenhouse gas emissions from water resource recovery facilities

2017

The emissions of the major greenhouse gases (GHGs), i.e. carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) from water resource recovery facilities (WRRFs) are of increasing concern in the water industry. In order to produce useful and comparable information for monitoring, assessing, and reporting GHG emissions from WRRFs, there is a need for a generally accepted methodology for their quantification. This paper aims at proposing the first protocol for monitoring and accounting for GHG emissions from WRRFs, taking into account both direct and indirect internal emissions and focusing the attention on plant sections known to be primarily responsible for GHG emissions (i.e. oxidation…

010504 meteorology & atmospheric sciences0208 environmental biotechnologyNitrous Oxide02 engineering and technologyWastewater01 natural sciencesMethaneCarbon footprint; Methane; Nitrous oxide; Off-gas; Wastewater; Energychemistry.chemical_compoundBiogasOff-ga0105 earth and related environmental sciencesResource recoveryCarbon FootprintEnergy recoveryEnergyWaste managementSettore ICAR/03 - Ingegneria Sanitaria-AmbientaleEnvironmental engineering020801 environmental engineeringAnaerobic digestionchemistryGreenhouse gasCarbon footprintEnvironmental scienceAerationMethane
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