Search results for "X-Ray"

showing 10 items of 4234 documents

Comparative analysis of numerical and experimental data of orthodontic mini-implants

2011

The purpose of this study was to compare numerical simulation data derived from finite element analysis (FEA) to experimental data on mini-implant loading. Nine finite element (FE) models of mini-implants and surrounding bone were derived from corresponding experimental specimens. The animal bone in the experiment consisted of bovine rib. The experimental groups were based on implant type, length, diameter, and angle of insertion. One experimental specimen was randomly selected from each group and was digitized in a microCT scanner. The FE models consisted of bone pieces containing Aarhus mini-implants with dimensions 1.5 × 7 mm and 1.5 × 9 mm or LOMAS mini-implants (dimensions 1.5 × 7 mm, …

Dental Stress AnalysisMaterials science9 mm caliberFinite Element AnalysisOrthodontics610 Medicine & health10067 Clinic for Orthodontics and Pediatric DentistryDisplacement (vector)Stress (mechanics)Imaging Three-DimensionalOrthodontic Anchorage ProceduresPerpendicularAnimalsOrthodontic Appliance DesignDental ImplantsModels Statisticalbusiness.industry3505 OrthodonticsBiomechanicsExperimental dataX-Ray MicrotomographyStructural engineeringFinite element methodBiomechanical PhenomenaCattleStress MechanicalbusinessRotation (mathematics)
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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
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Dynamic chemical devices: photoinduced electron transfer and its ion-triggered switching in nanomechanical butterfly-type bis(porphyrin)terpyridines.

2005

A series of butterfly-type molecular constructs has been prepared in good yield by using a double Stille coupling synthetic protocol. They are composed of a terpyridine (terpy) scaffold and two wings composed of appended porphyrins that are capable of switching from an extended W geometry to a compact U geometry upon cation coordination of the terpy unit. The porphyrin moieties exist in the constructs either as free bases or they can be sequentially metallated, thus giving rise to wings of different "colours". Stationary and time-resolved emission studies of the HZn, ZnAu and Zn2Au constructs show that the electronic properties are strongly dependent on the geometry. In the extended W confo…

DenticityMagnetic Resonance SpectroscopyPorphyrinsChemical PhenomenaPhotochemistryPyridinesMolecular ConformationElectronsPhotochemistryCrystallography X-RayLigandsCatalysisPhotoinduced electron transferchemistry.chemical_compoundElectron transferLigandHydrogen bondChemistry PhysicalOrganic ChemistryTemperatureGeneral ChemistryHydrogen-Ion ConcentrationPorphyrinZincSpectrometry FluorescencechemistryExcited stateSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIndicators and ReagentsSpectrophotometry UltravioletTerpyridineChemistry (Weinheim an der Bergstrasse, Germany)
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Field-Induced Slow Magnetic Relaxation in a Mononuclear Manganese(III)-Porphyrin Complex

2015

We report on a novel manganese(III)-porphyrin complex with the formula [Mn(III) (TPP)(3,5-Me2 pyNO)2 ]ClO4 ⋅CH3 CN (2; 3,5-Me2 pyNO=3,5-dimethylpyridine N-oxide, H2 TPP=5,10,15,20-tetraphenylporphyrin), in which the Mn(III) ion is six-coordinate with two monodentate 3,5-Me2 pyNO molecules and a tetradentate TPP ligand to build a tetragonally elongated octahedral geometry. The environment in 2 is responsible for the large and negative axial zero-field splitting (D=-3.8 cm(-1) ), low rhombicity (E/|D|=0.04) of the high-spin Mn(III) ion, and, ultimately, for the observation of slow magnetic-relaxation effects (Ea =15.5 cm(-1) at H=1000 G) in this rare example of a manganese-based single-ion ma…

DenticityPorphyrinsMetalloporphyrinsPyridineschemistry.chemical_elementManganese010402 general chemistryCrystallography X-RayLigands01 natural sciencesCatalysisIonlaw.inventionchemistry.chemical_compoundlawOctahedral molecular geometryMoleculeElectron paramagnetic resonanceComputingMilieux_MISCELLANEOUS[PHYS]Physics [physics]Manganese010405 organic chemistryLigandOrganic ChemistryElectron Spin Resonance SpectroscopyTemperatureGeneral ChemistryPorphyrin0104 chemical sciencesCrystallographychemistryMagnets
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Preparation and structural characterization of Ph3Sn(IV)+ complexes with pyridinecarboxylic acids or hydroxypyridene, -pyrimidine and –quinoline.

2006

A number of [Ph3Sn(IV)](+) complexes formed with ligands containing -OH (-C=O), or -COOH group(s) and aromatic IN) donor atom have been prepared. The binding sites of the ligands were identified by FT-IR spectroscopic measurements. In the complexes containing hydroxy and carboxylate functions, the carboxylato group is coordinated to the organotin(IV) centres in monodentate or bridging bidentate manner. It was also found that in the hydroxypyridine and -pyrimidine complexes the [Ph3Sn(IV)]+ moiety in most cases reacts with the phenolic form of the ligands. The rationalisation of the experimental Sn-119 Mossbauer nuclear quadrupole splittings, vertical bar Delta(exp)vertical bar - according t…

DenticityPyrimidineStereochemistrytriphenyltin(IV)BiochemistryMedicinal chemistryInorganic ChemistryMossbauerchemistry.chemical_compound2-HYDROXYPYRIDINEPyridineMaterials ChemistryMoietyCarboxylatePhysical and Theoretical ChemistryCOORDINATIONDERIVATIVESOrganic ChemistryQuinolineX-ray diffraction DICARBOXYLIC-ACIDShydroxypyridine -pyrimidine and pyridinecarboxylato complexeFT-IRTrigonal bipyramidal molecular geometryOctahedronchemistryLIGANDS
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A dinuclear rhodium(III) complex with the N,N′-ethylenebis(salicylideneiminato) (salen) ligand in a bridging bis-bidentate mode of coordination. Crys…

1990

In this communication we describe the synthesis and crystal structure of the complex [{Rh(η 2 -(C 6 H 4 )PPh 2 )(η 2 -P(o-ClC 6 H 4 )Ph 2 )} 2 (salen)]-(SbF 6 ) 2 , showing the bridging configuration of the salen ligand

DenticitySchiff baseStereochemistrychemistry.chemical_elementCrystal structureRhodiumInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMetal salen complexesSalen ligandX-ray crystallographyMaterials ChemistryMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
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Biomimetic Mn-catalases based on dimeric manganese complexes in mesoporous silica for potential antioxidant agent

2015

Two new structural and functional models of the Mn-catalase with formula [{Mn(III)(bpy)(H2O)}(μ-2-MeOC6H4CO2)2(μ-O){Mn(III)(bpy)(X)}]X, where X = NO3 (1) and ClO4 (2) and bpy = 2,2'-bipyridine, were synthesized and characterized by X-ray diffraction. In both cases, a water molecule and an X ion occupy the monodentate positions. The magnetic properties of these compounds reveal a weak antiferromagnetic behavior (2J = -2.2 cm(-1) for 1 and -0.7 cm(-1) for 2, using the spin Hamiltonian H = -2J S1·S2) and negative zero-field splitting parameter DMn (-4.6 cm(-1) and -3.0 cm(-1) for 1 and 2, respectively). This fact, together with the nearly orthogonal orientation of the Jahn-Teller axes of the M…

DenticitySilicon dioxideInorganic chemistrychemistry.chemical_elementManganeseCrystallography X-Ray010402 general chemistryLigands01 natural sciencesAntioxidantsCoordination complexBioinorganic chemistryInorganic ChemistryBipyridinechemistry.chemical_compoundBiomimeticsMoleculeManganèsPhysical and Theoretical ChemistryMaterialsComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationManganese010405 organic chemistryPhotoelectron SpectroscopyMesoporous silicaQuímica bioinorgànicaCatalaseSilicon Dioxide0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyLligandschemistryHybrid materialDimerization
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A novel coordination polymer with an unusual [3×2] oblique copper(II) grid: [Cu2(HBIMAM)2(C4O4)3(H2O)2]n·2nH2O [BIMAM=bis(imidazol-2-yl)methylaminome…

2013

Abstract This paper reports the synthesis, X-ray structure and magnetic characterization of [Cu2(HBIMAM)2(C4O4)3(H2O)2]n·2nH2O [BIMAM = bis(imidazol-2-yl)methylamino methane]. This compound is made of infinite chains – running along the [1 1 0] direction – with copper ions bridged by μ1,3-squarato ligands. Furthermore, these chains are further cross-linked through additional squarate anions (with the same μ1,3-bis(monodentate) bridging mode) to generate two-dimensional sheets parallel to the ab plane. There are inter-chains links every two copper atoms in a chain, forming an unusual (3 × 2) oblique copper(II) grid. Magnetic susceptibility measurements in the range 2–300 K show weak antiferr…

DenticityStereochemistryCoordination polymerX-rayOblique casechemistry.chemical_elementMagnetic susceptibilityCopperIonInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryPolyhedron
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Electronic properties and crystal structure of aqua (mepirizole-oxalato)copper(II)monohydrate: [Cu(C11H14N4O2)C2O4·H2O]H2O

1988

Abstract A Cu(ll) complex with mepirizole: 4-methoxy-2-(5-methoxy-3-methyl-pyrazoll-yl)-6-methylpyrimidine (L) and oxalate as ligands with the formula [CuL(C2O4)(H2O)]·H2O has been synthesized. The crystal structure has been determined by X-ray diffraction analysis: monoclinic, space group P21/n, Z = 4, a = 7.707(1), b = 14.951(3), c = 14.986(2) A,β = 92.40(2)°, V = 1725.2(8) A3, Dm = 1.61(1) g cm−3, Dc = 1.62 g cm−3, R = 0.032 and Rw = 0.035 for 2016 observed reflections. The CuN2O2O′chromophore can be described as square pyramidal strongly distorted towards trigonal bipyramidal. The basal coordination positions are occupied by the two oxygen atoms of the bidentate oxalate group, the coord…

DenticityStereochemistryCrystal structureOxalateSquare pyramidal molecular geometryInorganic Chemistrychemistry.chemical_compoundTrigonal bipyramidal molecular geometryCrystallographychemistryX-ray crystallographyMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryMonoclinic crystal systemPolyhedron
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NMR, X-Ray and MS Investigations of Ethyl 2-Aroyl-and Ethyl 2-Arylcarbamoyl-4,5- dimethyl-1,2,3,6-tetrahydropyridazine-1- carboxylates: Flexible Mult…

1999

The 1H and 13C NMR spectral assignments of ethyl 2-aroyl-4,5-dimethyl-1,2,3,6-tetrahydropyridazine-1-carboxylates (1a-1h) and ethyl 2-arylcarbamoyl-4,5-dimethyl-1,2,3,6-tetrahydropyridazine-1-carboxylates (2a-2k) are given based on DQF COSY, 1H,13C HMQC and 1H,13C HMBC-measurements; the dynamics of the tetrahydropyridazine ring has been studied by 1H, 1H EXSY-technique and the structure of one congener (4′-methylphenyl-derivative, 2a) has been confirmed by X-ray structure analysis.

DenticityStructure analysisStereochemistryChemistry010405 organic chemistryX-rayGeneral ChemistryCarbon-13 NMRRing (chemistry)010402 general chemistryMedicinal chemistry01 natural sciences0104 chemical sciencesJournal of Chemical Research
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