Search results for "FISICA APLICADA"

showing 10 items of 316 documents

Structural, magnetic and calorimetric studies of a crystalline phase of the spin crossover compound [Fe(tzpy)2(NCSe)2]

2013

The compound [Fe(tzpy)2(NCSe)2] (tzpy = 3-(2-pyridyl)-[1,2,3]triazolo[1,5-a]pyridine)) has been synthesized and its crystal structure, magnetic behavior and calorimetric properties investigated. Samples constituted of single crystals of [Fe(tzpy)2(NCSe) 2] display a relatively cooperative spin-state change centered at T1/2 ¿ 251.7 K with a hysteresis loop 3.5 K wide. The average enthalpy (¿H) and entropy (¿S) changes upon the spin crossover behavior (SCO) obtained from DSC measurements are 11.1 ± 0.4 kJ mol -1 and 44.5 ± 3 J K-1 mol-1, respectively. The magnetic and calorimetric data have been satisfactorily simulated using the mean-field regular solution model (Slichter-Drickamer) and the …

ChemistryIntermolecular forceEnthalpyRegular solutionGeneral ChemistryCrystal structureCondensed Matter Physicschemistry.chemical_compoundCrystallographySpin crossoverIntramolecular forceFISICA APLICADAPyridineGeneral Materials ScienceEntropy (order and disorder)
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{[Hg(SCN)3]2(n-L)}2-: An Efficient Secondary Building Unit for the Synthesis of 2D Iron(II) Spin-Crossover Coordination Polymers

2018

[EN] We report an unprecedented series of two-dimensional (2D) spin-crossover (SCO) heterobimetallic coordination polymers generically formulated as {Fe-II[(He(SCN)(3))(2)](L)(x))}center dot Solv, where x = 2 for L = tvp (trans-(4,4'-vinylenedipyridine)) (1tvp), bpmh ((1E,2E)-1,2-bis(pyridin-4-ylmethylene)hydrazine) (1bpmh center dot nCH(3)OH; n = 0, 1), by eh ( (1E,2E)-1,2-bis (1-(pyridin-4-yl) ethyliden e) hydrazine) (Ibpeh center dot nH(2)O; n = 0, 1) and x = 2.33 for L = 0 0 bpbz (1,4-bis(pyridin-4-yl)benzene) (1bpbz center dot nH(2)O; n = 0, 2/ 3). The results confirm that self-assembly of Fell, [Hg-II(SCN)(4)](2-), and ditopic rodlike bridging ligands L containing 4-pyridyl moieties f…

ChemistryLigandEnthalpySolvation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesLIESST0104 chemical sciencesInorganic ChemistrySolventchemistry.chemical_compoundCrystallographySpin crossoverFISICA APLICADAMoleculePhysical and Theoretical Chemistry0210 nano-technologyBenzene
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Spin crossover in iron(II) complexes with ferrocene-bearing triazole-pyridine ligands.

2015

In the search for new multifunctional spin crossover molecular materials, here we describe the synthesis, crystal structures and magnetic and photomagnetic properties of the complexes trans-[Fe(Fctzpy)2(NCX)2]·CHCl3 where Fc-tzpy is the ferrocene-appended ligand 4-(2-pyridyl)-1H-1,2,3-triazol- 1-ylferrocene, X = S (1) and X = Se (2). Both complexes display thermal- and light-induced (LIESST) spin crossover properties characterised by T1/2 = 85 and 168 K, ΔS = 55 and 66 J K−1 mol−1 , ΔH = 4.7 and 11.1 kJ mol−1 and TLIESST = 47 K and 39 K for 1 and 2 respectively. The crystal structure of 1 and 2 measured at 275 K is consistent with the iron(II) ion in the high-spin state while the crystal st…

ChemistryLigandTriazoleCrystal structureLIESSTPyridine ligandIonInorganic Chemistrychemistry.chemical_compoundCrystallographyNuclear magnetic resonanceFerroceneSpin crossoverFISICA APLICADADalton transactions (Cambridge, England : 2003)
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Organocatalytic asymmetric addition of naphthols and electron-rich phenols to isatin-derived ketimines: highly enantioselective construction of tetra…

2015

A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols and activated phenols to ketimines derived from isatins. The reaction afforded chiral 3-amino-2-oxindoles with a quaternary stereocenter in high yields (up to 99%) with excellent enantioselectivity (up to 99% ee). To the best of our knowledge, this transformation is the first highly enantioselective addition of naphthols to ketimines

ChemistryOrganocatalysisIsatinIsatin-derived ketiminesEnantioselective synthesisAsymmetric synthesisGeneral ChemistryNaphtholsGeneral MedicineCatalysisStereocenterReaccions químiqueschemistry.chemical_compoundThioureaCatàlisiOrganocatalysisFISICA APLICADAOrganic chemistryPhenolsFriedel-Crafts reactionsQuímica orgànicaAngewandte Chemie (International ed. in English)
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Diastereoselective Michael addition of (S)-mandelic acid enolate to 2-arylidene-1,3-diketones: enantioselective diversity-oriented synthesis of dense…

2006

[EN] A diversity-oriented approach to enantiomerically pure densely substituted pyrazoles, ¿-aryl-¿-pyrazolylatrolactic acid and ¿-aryl-¿-pyrazolylacetophenones has been developed. The approach utilises the conjugated addition of the lithium enolate of the (2S,5S)-cis-1,3-dioxolan-4-one derived from optically active (S)-mandelic acid and pivalaldehyde to several 2-arylidene-1,3-diketones, which proceeds readily to give the corresponding Michael adducts in good yields and diastereoselectivities. The cyclocondensation of the 1,3-diketone moieties present in Michael adducts with several hydrazines leads to enantiomerically pure densely substituted pyrazoles. Subsequent basic hydrolysis of the …

ChemistryStereochemistryOrganic ChemistryEnantioselective synthesisGeneral MedicineConjugated systemMandelic acidBiochemistryMedicinal chemistryCatalysisAdductchemistry.chemical_compoundFISICA APLICADADrug DiscoveryMichael reactionMoietyOrganic chemistryOxidative decarboxylation
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Stereopsis assessment at multiple distances with an iPad application

2017

[EN] We present a new application for iPad for screening stereopsis at multiple distances that allows testing up to ten levels of stereoacuity at each distance. Our approach is based on a random dot stereogram viewable with anaglyph spectacles. Sixty-five subjects with no ocular diseases, wearing their habitual correction were measured at 3 m and 0.5 m. Results were compared with a standard stereoscopic test (TNO). We found not statistically significant differences between both tests, but our method achieved higher reproducibility. Applications in visual screening programs and to design and use of 3D displays, are suggested. (C) 2017 Elsevier B.V. All rights reserved.

Computer science3D displaysStereoacuityIPad02 engineering and technologyStereo displayHuman-Computer InteractionStereoscopic acuity03 medical and health sciences0302 clinical medicineStereopsisDepth perceptionHardware and ArchitectureComputer graphics (images)FISICA APLICADA030221 ophthalmology & optometry0202 electrical engineering electronic engineering information engineering020201 artificial intelligence & image processingElectrical and Electronic EngineeringScreening stereopsisBinocular visionDepth perceptionBinocular vision
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Perfiles de potencia de las lentes de contacto medidas con NIMO TR1504

2017

This study was supported by the Ministerio de Economía y Competitividad and FEDER (Grant DPI2015-71256-R) and by the Generalitat Valenciana (Grant PROMETEOII-2014-072), Spain.

Contact LensesComputer sciencebusiness.industryRefraction OcularRefraction03 medical and health sciencesOcular physiology0302 clinical medicineOpticslcsh:Ophthalmologylcsh:RE1-994FISICA APLICADA030221 ophthalmology & optometryHumanslcsh:QC350-467businessScientific LetterAlgorithmsSoftware030217 neurology & neurosurgerylcsh:Optics. LightOptometry
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Thermal-, pressure- and light-induced spin-crossover behviour in the two-dimensional Hofman-like coordination polymer [Fe(3-Clpy)2Pd(CN)4]

2013

The thermal spin-crossover behaviour, photoexcitation and subsequent relaxation, as well as the pressure-induced spincrossover behaviour at 298 K are discussed for the non-porous two-dimensional Hofmann-like coordination polymer [Fe(3-Clpy)(2)Pd(CN)(4)] (1). The title compound undergoes a two-step, cooperative thermal-induced SCO with critical temperatures T-c1(down arrow) = 159.6 K and T-c1(up arrow) = 164.5 K for the first step and T-c2(down arrow) = 141.4 K and T-c2(up arrow) = 148.4 K for the second step. Irradiation of the low-spin state with green light (514 nm) at 10 K induced the photoexcitation of around 60% of the iron(II) centres to the high-spin state (LIESST effect). The subseq…

Coordination polymerIronEnthalpyCooperativity02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesLIESSTAbsorptionInorganic Chemistrychemistry.chemical_compoundSpin crossoverRelaxation (NMR)[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPhotomagnetismSpin crossover0104 chemical sciencesPhotoexcitationCoordination polymersCrystallographychemistryFISICA APLICADA0210 nano-technologyPhotomagnetism
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An Na8 Cluster in the Structure of a Novel oxamato-bridged Na'Cu'' three-Dimensional Coordination Polymer

1999

[EN] The new heterometallic sodium(I)¿copper(II) compound Na4Cu2 (2) · 10.5 H2O (3), where H8[2] stands for N,N',N'',N'''-methanetetrayltetrakismethylenetetrakis(oxamic acid), has been synthesized and its crystal structure determined by single-crystal X-ray diffraction. The structure of 3 consists of cationic [Cu2(¿4:¿4-2)]4- dinuclear units, coordinated sodium cations, and water molecules. In the crystal, the dinuclear copper entities are joined through discrete aggregates of eight sodium atoms linked by oxamato and water bridges, leading to a three-dimensional polymeric network.

Coordination polymerStereochemistrySodiumSodiumCationic polymerizationchemistry.chemical_elementCrystal structureAmidesInorganic ChemistryCrystalClusterschemistry.chemical_compoundCrystallographychemistryFISICA APLICADACluster (physics)MoleculeChiralityChirality (chemistry)Copper
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Crystal structure of the coordination polymer [FeIII2{PtII(CN)4}3]

2015

[EN] The title complex, poly[dodeca--cyanido-diiron(III)triplatinum(II)], [FeIII2{PtII(CN)4}3], has a three-dimensional polymeric structure. It is built-up from square-planar [PtII(CN)4] 2 anions (point group symmetry 2/m) bridging cationic [FeIIIPtII(CN)4] + 1 layers extending in the bc plane. The FeII atoms of the layers are located on inversion centres and exhibit an octahedral coordination sphere defined by six N atoms of cyanide ligands, while the PtII atoms are located on twofold rotation axes and are surrounded by four C atoms of the cyanide ligands in a square-planar coordination. The geometrical preferences of the two cations for octahedral and square-planar coordination, respectiv…

Coordination sphereCoordination polymerStereochemistryCyanide02 engineering and technologyCrystal structure010402 general chemistry01 natural scienceschemistry.chemical_compoundSpin crossoverMolecular symmetryGeneral Materials ScienceSpin-crossoverCrystallographyCrystal structureCationic polymerizationGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsData Reports0104 chemical sciencesCrystallographychemistryQD901-999FISICA APLICADAPolycyanidometalate0210 nano-technologyActa Crystallographica Section E Crystallographic Communications
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