Search results for "ceramic"

showing 10 items of 2129 documents

Asymmetric [N–I–N]+halonium complexes in solution?

2020

Assessment of the solution equilibria of [bis(pyridine)iodine(I)]+ complexes by ESI-MS and NMR reveals the preference of iodine(I) to form complexes with a more basic pyridine. Mixtures of symmetric [bis(pyridine)iodine(I)]+ complexes undergo statistical ligand exchange, with a predominant entropic driving force favoring asymmetric systems. The influence of ligand basicity, concentration, temperature, and ligand composition is evaluated. Our findings are expected to facilitate the investigations, and the supramolecular and synthetic applications of halonium ions’ halogen bonds. peerReviewed

inorganic chemicals2019-20 coronavirus outbreakliuoksetLigandMetals and AlloysSupramolecular chemistrychemistry.chemical_elementliganditkompleksiyhdisteetGeneral ChemistryIodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonjodichemistry.chemical_compoundchemistryPyridineHalogenMaterials ChemistryCeramics and CompositesHalonium ionChemical Communications
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Potent affinity material for tracing acetone and related analytes based on molecular recognition by halogen bonds.

2014

Affinity materials based on halogen bonds turned out to be a powerful tool for the molecular recognition of acetone or related carbonyl compounds in the presence of ubiquitous protic molecules. The superior selectivity and sensitivity were found by the gravimetric detection of volatile organic compounds by quartz crystal microbalances.

inorganic chemicalsAnalyteMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystalchemistry.chemical_compoundMolecular recognitionchemistryHalogenMaterials ChemistryCeramics and CompositesAcetoneMoleculeOrganic chemistryGravimetric analysisSelectivityChemical communications (Cambridge, England)
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Structural Changes of Titanium Oxide Induced by Chromium Addition as Determined by an X-Ray Diffraction Study

1995

Abstract An X-ray diffraction study has been carried out on a series of polycrystalline TiO 2 (anatase) catalysts containing Cr(III) at different atomic concentrations (0.2-5.0 at. %), prepared by a co-precipitation method. Analysis of the variation of the unit cell parameters of chromium-doped anatase with respect to pure anatase has allowed us to estimate the solubility limit for the system at around 1.4 at. %. There is no evidence for the existence of a separate crystalline chromium oxide phase. Temperature effects on the cell parameter and on the anatase-rutile transformation rate were also analyzed. An increase in temperature produced release of the chromium from the solid solution. At…

inorganic chemicalsAnataseMaterials scienceInorganic chemistrytechnology industry and agricultureAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsTitanium oxideInorganic ChemistryChromiumchemistryPhase (matter)X-ray crystallographyMaterials ChemistryCeramics and CompositesCrystallitePhysical and Theoretical ChemistrySolubilitySolid solutionJournal of Solid State Chemistry
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Iron(iii) oxamato-catalyzed epoxidation of alkenes by dioxygen and pivalaldehyde

1997

A new iron(III)–carbonato monomeric complex of orthophenylenebis( oxamato) (opba) 1 is synthesized, and spectroscopically and structurally characterized; it is a moderately efficient non-heme catalyst for the aerobic epoxidation of alkenes with co-oxidation of pivalaldehyde. Ruiz Garcia, Rafael, Rafael.Ruiz@uv.es ; Fernandez Picot, Isabel, Isabel.Fernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es

inorganic chemicalsDioxygenUNESCO::QUÍMICA::Química inorgánicaUNESCO::QUÍMICAorganic chemicalsIronMetals and AlloysIron ; Dioxygen ; Orthophenylenebis ; Catalyst ; PivalaldehydeGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCeramics and Compositesheterocyclic compoundsCatalystOrthophenylenebisPivalaldehyde
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Tetraiodoethynyl resorcinarene cavitands as multivalent halogen bond donors

2014

The first examples of iodoethynyl resorcinarene cavitands as rigid 3D halogen bond (XB) donor molecules are presented. These concave macrocycles form strong, RXB = 0.78–0.83, halogen bonds with dioxane oxygen, pyridine nitrogen and a bromide anion in tetraproropyl ammonium bromide resulting in deep cavity cavitand structures.

inorganic chemicalsHalogen bondChemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryResorcinarenePhotochemistryOxygenNitrogenCatalysis3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundBromidePolymer chemistryHalogenMaterials ChemistryCeramics and Compositesta116Chemical communications
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Graphitically encapsulated cobalt nanocrystal assemblies

2010

Graphitically encapsulated cobalt nanocrystal assemblies are chemically prepared by one-pot reaction at380 degrees C followed by a reversed etching process to produce porous graphitic structure for revealing their self-assembling nature.

inorganic chemicalsHot TemperatureMaterials sciencefungitechnology industry and agricultureMetals and Alloyschemistry.chemical_elementNanotechnologyCobaltGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMagneticschemistryNanocrystalEtching (microfabrication)Scientific methodMaterials ChemistryCeramics and CompositesNanoparticlesPorosityPorosityCobaltChemical Communications
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Cocrystal trimorphism as a consequence of the orthogonality of halogen- and hydrogen-bonds synthons.

2019

True trimorphic cocrystals, i.e. multi-component molecular crystals of identical composition that exhibit three polymorphic structures, are exceedingly rare and so far no halogen-bonded cocrystal system has been reported to exhibit trimorphism. Here we describe a unique example of a trimorphic cocrystal exhibiting both hydrogen and halogen bonds in which the differences between polymorphs reveal their orthogonality, evident by the apparently independent variation of well-defined hydrogen- and halogen-bonded motifs. peerReviewed

inorganic chemicalsHydrogenchemistry.chemical_element010402 general chemistry01 natural sciencesCocrystalCatalysiskemialliset sidoksetOrthogonalityTrimorphismMaterials Chemistrysupramolekulaarinen kemiavetysidokset010405 organic chemistryHydrogen bondSynthonMetals and Alloysorthogonality halogen bond hydrogen bond cocrystal trimorphismGeneral Chemistrykiteet0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryHalogenCeramics and CompositesChemical communications (Cambridge, England)
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Creation of glass-characteristic point defects in crystalline SiO2 by 2.5 MeV electrons and by fast neutrons

2019

The support from M -ERANET project “MyND” is acknowledged. K.K. was partially supported by the Collaborative Research Project of Laboratory for Materials and Structures, Tokyo Institute of Technology . Visiting researcher support from Ecole Polytechnique, Palaiseau is appreciated. Mr. Olivier Cavani is thanked for the expert help with irradiations.

inorganic chemicalsLuminescenceMaterials science02 engineering and technologyCrystal structure01 natural sciencesMolecular physicsCrystal0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]Materials ChemistryElectron beam processingIrradiationDangling bonds[PHYS]Physics [physics]010302 applied physicstechnology industry and agricultureDangling bondElectron irradiationQuartz021001 nanoscience & nanotechnologyCondensed Matter PhysicsCrystallographic defectAmorphizationNeutron temperatureElectronic Optical and Magnetic MaterialsAmorphous solidCeramics and CompositesSilica glass0210 nano-technologyJournal of Non-Crystalline Solids
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Influence of Ge doping level on the EPR signal of Ge(1), Ge(2) and E'Ge defects in Ge-doped silica

2011

Abstract We present an experimental investigation on the Ge doping level dependence of the Electron Paramagnetic Resonance (EPR) signal spectral features of the Ge(1), Ge(2) and E'Ge defects induced in Ge doped silica. We have studied samples produced by sol–gel or PCVD techniques and doped with different amounts of Ge up to 20% by weight. The samples were gamma or beta ray irradiated and successively they were thermally treated to isolate the EPR signals of the different point defects. The data show that the EPR line shapes of the Ge(1) and the Ge(2) centers are progressively modified for doping level higher than 1%, whereas the line shape of the E'Ge defect appears independent from the do…

inorganic chemicalsMaterials scienceAnalytical chemistrychemistry.chemical_elementGermaniumSilica paramagnetic point defects Ge-doped silicasilice drogata difetti di punto risonanza magneticalaw.inventionsymbols.namesakeraman spectroscopylawCondensed Matter::SuperconductivityBeta particleMaterials ChemistryIrradiationElectron paramagnetic resonanceSol-gelSettore FIS/01 - Fisica SperimentaleDopingtechnology industry and agricultureCondensed Matter PhysicsCrystallographic defectElectronic Optical and Magnetic MaterialschemistryCeramics and Compositessymbolslipids (amino acids peptides and proteins)Condensed Matter::Strongly Correlated ElectronsRaman spectroscopyhuman activitiesJournal of Non-Crystalline Solids
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Synthesis and Characterisation of Functionalized borosilicate nanoparticles for boron neutron capture therapy applications

2012

Boron Neutron Capture Therapy (BNCT) is a promising therapy for the cure of diffuse tumors. The successful clinical application of BNCT requires finding new boron-based compounds suitable for an efficient 10B delivery to the cancerous tissues. The purpose of this work is to synthesize borosilicate nanoparticles by a sol–gel recipe, and to functionalize them with folic acid in order to promote their capture by the tumor cells. Whereas sol–gel is a promising technique for the synthesis of nanoparticles, in case of borosilicate systems this approach is affected by significant boron loss during preparation. Here we show that functionalization of borosilicate nanoparticles with folic acid can re…

inorganic chemicalsMaterials scienceBiocompatibilityFolic acidNanoparticles Borosilicate Folic acid BNCTchemistry.chemical_elementNanoparticleNanotechnologyBiomaterialsNanoparticleBorosilicateMaterials ChemistryReactivity (chemistry)BoronBorosilicate glassGeneral ChemistryCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsNeutron capturechemistryFolic acidCeramics and CompositesBNCTSurface modificationNanoparticlesNuclear chemistry
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