Search results for "reo"

showing 10 items of 7464 documents

Integral-Imaging display from stereo-Kinect capture

2017

In this paper, we propose a new approach in order to improve the quality of microimages and display them onto an integral imaging monitor. Our main proposal is based on the stereo-hybrid 3D camera system. Originally, hybrid camera system has dissimilarity itself. We interpret our method in order to equalize the hybrid sensor's characteristics and 3D data modification strategy. We generate integral image by using synthetic back-projection mapping method. Finally, we project the integral image onto our proposed display system. We illustrate this procedure with some imaging experiments in order to prove an advantage of our approach.

010302 applied physicsIntegral imagingbusiness.industryComputer scienceComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONPoint cloudStereo display01 natural sciencesÒptica Aparells i instrumentsImage (mathematics)010309 opticsComputer graphics (images)0103 physical sciences3d cameraComputer visionArtificial intelligencebusinessThree-Dimensional Imaging, Visualization, and Display 2017
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Binocular function measures as predictors of user performance in stereoscopic augmented reality

2021

Inconsistency between the binocular and focus cues in stereoscopic augmented reality overburdens the visual system leading to its stress. However, a high individual variability of tolerance for visual stress makes it difficult to predict and generalize the user gain associated with the implementation of alternative visualization technologies. In this study, we investigated the relationship between the binocular function and perceptual judgments in augmented reality. We assessed the task completion time and accuracy of perceptual distance matching depending on the consistency of binocular and focus cues in the stereoscopic environment of augmented reality. The head-mounted display was driven…

010302 applied physicsMatching (statistics)genetic structuresbusiness.industryComputer sciencemedia_common.quotation_subjectStereoscopy01 natural scienceseye diseaseslaw.inventionVisualization010309 opticslawPerception0103 physical sciencesStress (linguistics)Contrast (vision)Computer visionAugmented realityArtificial intelligencebusinessFocus (optics)media_common
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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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A solvent-directed stereoselective and electrocatalytic synthesis of diisoeugenol.

2018

A stereoselective and electrocatalytic coupling reaction of isoeugenol has been reported for the first time in a 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP)/boron-doped diamond (BDD) electrode system. This particular C-C bond formation and diastereoselectivity is driven by a solvate interaction between the radical species and another isoeugenol molecule. Due to an electrocatalytic cycle, only understoichiometric amounts of charge are necessary. Since electric current is directly employed as the oxidant, the reaction is metal and reagent-free. In addition, the electrolysis can be conducted in a very simple undivided beaker-type cell under constant current conditions. Therefore, the protocol is …

010402 general chemistry01 natural sciencesCatalysisCoupling reactionlaw.inventionMetalchemistry.chemical_compoundlawMaterials ChemistryMoleculeElectrolysis010405 organic chemistryMetals and AlloysGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventIsoeugenolchemistryvisual_artElectrodeCeramics and Compositesvisual_art.visual_art_mediumStereoselectivityChemical communications (Cambridge, England)
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A versatile rigid binucleating ligand for Rh2(μ-Cl)2 moieties: its application as a catalyst in hydrogenation and cyclopropanation

2003

A rigid non-deforming "MCl 2 M" binucleating ligand [7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 ] - able to held the two rhodium atoms in a cooperative distance has been synthesized. The original two bridging chlorides are retained in [Rh 2 (C 5 Me 5 ) 2 Cl 2 {7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + . Hydrogenation of 1-hexene is 10 times faster with [Rh 2 (C 5 Me 5 ) 2 Cl 2 {7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + than with [Rh 2 (C 5 Me 5 ) 2 Cl 4 ]. A hydrogenation mechanism has been proposed which assumes that [Rh 2 (C 5 Me 5 ) 2 (Cl)(H){7,8-μ-S(4'-C 6 H 3 (CH 3 ))S-C 2 B 9 H 1 0 }] + is the first generated species in the process.

010405 organic chemistryChemistryCyclopropanationStereochemistryOrganic Chemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryRhodium compounds0104 chemical sciencesCatalysisRhodiumInorganic ChemistryMaterials ChemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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A new hydrogen bonding motif involved in self-recognition in the solid state by functionalised macrocycles

2011

Self-recognition within the crystal lattices of three functionalised macrocycles results in the formation of arrays of remarkably similar hermaphroditic pairs of macrocycles. In the case of two of the macrocycles containing acylhydrazine substituents, a hitherto unknown recognition pattern is found in the interaction of the hydrazine moiety with crown-ether oxygen atoms.

010405 organic chemistryChemistryHydrogen bondStereochemistryHydrazineAcylhydrazineSolid-stateGeneral ChemistrySelf recognitionCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences3. Good health0104 chemical scienceschemistry.chemical_compoundOxygen atomPolymer chemistryMoiety[CHIM]Chemical SciencesGeneral Materials Scienceta116ComputingMilieux_MISCELLANEOUS
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Sulfur, tin and gold derivatives of 1-(2'-pyridyl)-ortho-carborane, 1-R-2-X-1,2-C2B10H10 (R = 2'-pyridyl, X = SH, SnMe3 or AuPPh3).

2004

Reaction of the lithium salt of 1-(2'-pyridyl)-ortho-carborane, Li[1-R-1,2-C(2)B(10)H(10)](R = 2'-NC(5)H(4)), with sulfur, followed by hydrolysis, gave the mercapto-o-carborane, 1-R-2-SH-1,2-C(2)B(10)H(10) which forms chiral crystals containing helical chains of molecules linked by intermolecular S-H...N hydrogen bonds. The cage C(1)-C(2) and exo C(2)-S bond lengths (1.730(3) and 1.775(2)[Angstrom], respectively) are indicative of exo S=C pi bonding. The tin derivative 1-R-2-SnMe(3)-1,2-C(2)B(10)H(10), prepared from Li[1-R-1,2-C(2)B(10)H(10)] and Me(3)SnCl, crystallises with no significant intermolecular interactions. The pyridyl group lies in the C(1)-C(2)-Sn plane, oriented to minimise th…

010405 organic chemistryChemistryHydrogen bondStereochemistryIntermolecular forcechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryBond lengthCrystallographyTrigonal bipyramidal molecular geometryCarboraneMoleculeTinDalton transactions (Cambridge, England : 2003)
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Access to α-Aminophosphonic Acid Derivatives and Phosphonopeptides by [Rh(P–OP)]-Catalyzed Stereoselective Hydrogenation

2020

The hydrogenation of N-substituted vinylphosphonates using rhodium complexes derived from P–OP ligands L1, ent-L1, or (R,R)-Me-DuPHOS as catalysts has been successfully accomplished, achieving very high levels of stereoselectivity (up to 99% ee or de). The described synthetic strategy allowed for the efficient preparation of α-aminophosphonic acid derivatives and phosphonopeptides, which are valuable building blocks for the preparation of biologically relevant molecules.

010405 organic chemistryChemistryLigandOrganic Chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisRhodiumDerivative (finance)MoleculeStereoselectivityJournal of Organic Chemistry
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Structural, photophysical and magnetic properties of transition metal complexes based on the dipicolylamino-chloro-1,2,4,5-tetrazine ligand

2015

International audience; The ligand 3-chloro-6-dipicolylamino-1,2,4,5-tetrazine (Cl-TTZ-dipica) 1, prepared by the direct reaction between 3,6-dichloro-1,2,4,5-tetrazine and di(2-picolyl)-amine, afforded a series of four neutral transition metal complexes formulated as [Cl-TTZ-dipica-MCl2]2, with M = Zn(II), Cd(II), Mn(II) and Co(II), when reacted with the corresponding metal chlorides. The dinuclear structure of the isostructural complexes was disclosed by single crystal X-ray analysis, clearly indicating the formation of [MII–(μ-Cl)2MII] motifs and the involvement of the amino nitrogen atom in semi-coordination with the metal centers, thus leading to distorted octahedral coordination geome…

010405 organic chemistryChemistryLigandStereochemistrySubstituentSupramolecular chemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundTetrazineCrystallographyTransition metalvisual_artIntramolecular forceddc:540visual_art.visual_art_medium[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryIsostructuralComputingMilieux_MISCELLANEOUSDALTON TRANSACTIONS
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Regioselective Synthesis of Mono- and Dispiropyrazoline Derivatives via 1,3-dipolar Cycloaddition with Nitrilimines

2016

The 1,3-dipolar cycloaddition reaction of (E,E)-1,3-bis(arylidene)indan-2-one with diarylnitrilimines, generated in situ via dehydrohalogenation of the corresponding hydrazonoyl chlorides , affords predominantly monospiropyrazolines and as a mixture of diastereoisomers. Also dispiropyrazolines are formed in moderate yields. The structure and stereochemistry of cycloadducts were confirmed by 1H and 13C-NMR spectroscopy, elemental analyses data, and single-crystal X-ray diffraction studies of and .

010405 organic chemistryChemistryOrganic ChemistryDiastereomerRegioselectivity010402 general chemistry01 natural sciencesMedicinal chemistryCycloaddition0104 chemical sciences13-Dipolar cycloadditionDehydrohalogenationOrganic chemistrySpectroscopyJournal of Heterocyclic Chemistry
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