Search results for "FISICA APLICADA"

showing 10 items of 316 documents

Organocatalytic Enantioselective Friedel-Crafts Alkylation of 1-Naphthol Derivatives and Activated Phenols with Ethyl Trifluoropyruvate

2015

An organocatalytic enantioselective Friedel–Crafts alkylation of a series of substituted 1- naphthol derivatives and activated phenols with ethyl trifluoropyruvate, catalyzed by a quinine-derived squaramide, is presented. Good yields and high to excellent enantioselectivities of the Friedel– Crafts alkylation products were obtained.

biologyOrganocatalysis1-NaphtholEnantioselective synthesisGeneral ChemistryNaphtholsbiology.organism_classificationTrifluoropyruvatesReaccions químiqueschemistry.chemical_compoundEthyl trifluoropyruvatechemistryCatàlisiOrganocatalysisFISICA APLICADAAsymmetric catalysisOrganic chemistryPhenolsValenciaFriedel–Crafts reactionQuímica orgànicaFriedel–Crafts reaction
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Strong Cooperative Spin Crossover in 2D and 3D FeII −MI,II HofmannLike Coordination Polymers Based on 2‑Fluoropyrazine

2016

Self-assembling iron(II), 2-fluoropyrazine (Fpz), and [MII(CN)4] 2− (MII = Ni, Pd, Pt) or [AuI (CN)2] − building blocks have afforded a new series of two- (2D) and threedimensional (3D) Hofmann-like spin crossover (SCO) coordination polymers with strong cooperative magnetic, calorimetric, and optical properties. The iron(II) ions, lying on inversion centers, define elongated octahedrons equatorially surrounded by four equivalent centrosymmetric μ4-[MII(CN)4]2− groups. The axial positions are occupied by two terminal Fpz ligands affording significantly corrugated 2D layers {Fe(Fpz)2([MII(CN)4]}. The Pt and Pd derivatives undergo thermal- and light-induced SCO characterized by T1/2 temperatur…

chemistry.chemical_classification010405 organic chemistryPolymer010402 general chemistry01 natural sciences0104 chemical sciencesIonInorganic ChemistryCrystallographyNuclear magnetic resonancechemistrySpin crossoverFISICA APLICADAPhysical and Theoretical Chemistry
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Switchable Spin-Crossover Hofmann-Type 3D Coordination Polymers Based on Tri- and Tetratopic Ligands

2018

[EN] Fe-II spin-crossover (SCO) coordination polymers of the Hofmann type have become an archetypal class of responsive materials. Almost invariably, the construction of their architectures has been based on the use of monotopic and linear ditopic pyridine like ligands. In the search for new Hofmann-type architectures with SCO properties, here we analyze the possibilities of bridging ligands with higher connectivity degree. More precisely, the synthesis and structure of {Fe-II(L-N3)[M-I(CN)(2)](2)}center dot(Guest) (Guest = nitro-benzene, benzonitrile, o-dichlorobenzene; M-I = Ag, Au) and {Fe-II(L-N4)[Ag-2(CN)(3)][Ag(CN)(2)]}center dot H2O are described, where L-N3 and L-N4 are the tritopic…

chemistry.chemical_classification010405 organic chemistryPolymerType (model theory)010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryNitrobenzenechemistry.chemical_compoundBenzonitrileCrystallographychemistrySpin crossoverFISICA APLICADAPhysical and Theoretical ChemistryBenzene
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Pressure Effect Studies on the 3D Spin Crossover System: {Fe(3CN-py)2[M(CN)2]2}·nH2O (n < 2/3, M = Ag(I), Au(I))

2007

[EN] Pressure effect investigations on the magnetic behaviour of the 3D SCO polymers {Fe(3CN-py)2[Ag(CN)2]2} · 2/3H2O (1) and {Fe(3CN-py)2[Au(CN)2]2} · 2/3H2O (2) have been carried out in the range of 105 Pa to 0.7 GPa. Despite both compounds are isostructural their magnetic behaviour under applied hydrostatic pressures is very different. Strong nonlinearity in the Tc(P) vs. P plot has been observed for compound 1 a fact which contrasts with the almost linear dependence observed for each spin transition in 2. However, both compounds are extremely sensitive to the application of pressure as well as the Tc(P) vs. P plots denote.

chemistry.chemical_classificationCrystallographychemistryCondensed matter physicsSpin crossoverFISICA APLICADASpin transitionGeneral Physics and AstronomyPolymerPhysical and Theoretical ChemistryIsostructural
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Fabrication of Single Cylindrical Au-Coated Nanopores with Non-Homogeneous Fixed Charge Distribution Exhibiting High Current Rectifications

2014

We have designed and characterized a cylindrical nanopore that exhibits high electrochemical current rectification ratios at low and intermediate electrolyte concentrations. For this purpose, the track-etched single cylindrical nanopore in polymer membrane is coated with a gold (Au) layer via electroless plating technique. Then, a non-homogeneous fixed charge distribution inside the Au-coated nanopore is obtained by incorporating thiol-terminated uncharged poly(N-isopropylacrylamide) (PNIPAM) chains in series to poly(4-vinyl pyridine) (PVP) chains, which are positively charged at acidic pH values. The functionalization reaction is checked by measuring the current–voltage (I–V) curves prior …

chemistry.chemical_classificationElectroless gold platingMaterials scienceCurrent rectificationNernst−Planck equationsNanotechnologyPolymerElectrolyteElectrochemistryIonStimuli-responsive polymersNanoporeAdsorptionMembranechemistryChemical engineeringChemisorptionFISICA APLICADAGeneral Materials ScienceSynthetic nanoporesChemical functionalization
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Two-dimensional assembling of 4,4'-bipyridine and 4,4'-azopyridine bridged iron(II) linear coordination polymers via hydrogen bond

1999

[EN] Novel two-dimensional polymers, [Fe(L-1)(H2O)(2)(NCX)(2)]. L-1 (L-1 =4.4'-bipyridine (bipy)) (1, 2) and [Fe(L-2)(CH3OH)(2)-(NCX)(2)]. L-2 (L-2 =4,4'-azopyridine (azpy)) (3) and X = S (1, 3), Se (2), have been synthesized and characterized by X-ray crystallography. The structures reveal the formation of tranzs-L-bridged [Fe(NCX)(2)(Y)(2)] where Y=H2O, CH3OH linear chains assembled into two-dimensional networks by hydrogen bonds between the uncoordinated ligand L and the coordinated solvent molecules.

chemistry.chemical_classificationHydrogen bondLigandPolymerCrystal structureIron complexes44'-BipyridineInorganic ChemistrySolventCrystallographychemistry.chemical_compoundchemistryFISICA APLICADASelf assemblingCrystal structuresMaterials ChemistryMoleculePhysical and Theoretical ChemistrySelf-assemblingCoordination polymer complexes
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Catalytic enantioselective addition of terminal alkynes to aromatic aldehydes using zinc-hydroxyamide complexes

2009

[EN] A mandelamide ligand, derived from (S)-mandelic acid and (S)-phenylethanamine, catalyzes the addition of aryl-, alkyl-and silyl-alkynylzinc reagents to aromatic and heteroaromatic aldehydes with good yields and good to high enantioselectivities.

chemistry.chemical_classificationLigandArylOrganic ChemistryEnantioselective synthesischemistry.chemical_elementZincBiochemistryCatalysischemistry.chemical_compoundchemistryFISICA APLICADAReagentOrganic chemistryPhysical and Theoretical ChemistryAlkylMandelamideOrganic &amp; Biomolecular Chemistry
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Chemistry and reactivity of mononuclear manganese oxamate complexes: Oxidative carbon-carbon bond cleavage of vic-diols by dioxygen and aldehydes cat…

2006

[EN] Two new mononuclear octahedral manganese(III) complexes with the tetradentate equatorial ligand o-phenylenebis(oxamate) (opba) and two aquo (1a) or two pyridine (1b) axial ligands have been synthesized and characterized structurally, magnetically, and electrochemically. The cyclovoltammogram of 1a in acetonitrile (25 degrees C, 0.1 M Bu4NPF6) shows an irreversible one-electron oxidation peak at a high anodic potential (E-ap = 1.03 V versus SCE), while that of 1b shows two well-separated one-electron oxidation peaks at moderate to high anodic potentials (E-ap = 0.92 and 1.27 V versus SCE), the first redox-wave being quasireversible in nature. The access to formally high-valent Mn-IV and…

chemistry.chemical_classificationO-O bond activationManganesePivalic acidLigandStereochemistryProcess Chemistry and Technologychemistry.chemical_elementManganeseC-C bond activationMedicinal chemistryAldehydeRedoxCatalysischemistry.chemical_compoundchemistryCarbon–carbon bondOxidationsFISICA APLICADAPyridinePhysical and Theoretical ChemistryBond cleavageRedox properties
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Manganese(III)-mediated oxidative carbon-carbon bond cleavage of the 1,10-phenanthroline-5,6-dione ligand

1999

[EN] A new manganese(III)-1,10-phenanthroline-5,6-dione (phendione) complex possessing a putative Mn-2(mu-O) (mu-O2CMe)(2) core has been found to undergo a Ligand-based oxidative cleavage of the C(5)-C(6) bond in weak acid aqueous MeOH under aerobic conditions at room temperature to yield 2,2'-bipyridyl-3,3'-dicarboxylate with co-reduction to the corresponding Mn-II-phendione species.

chemistry.chemical_classificationQuinone complexesPolynuclear complexesAqueous solutionLigandCarboxylato complexesPhenanthrolinechemistry.chemical_elementCrystal structureManganesePhotochemistryCleavage (embryo)Medicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryCarbon–carbon bondYield (chemistry)FISICA APLICADACrystal structuresOxidationMaterials ChemistryPhysical and Theoretical ChemistryManganese complexes
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Thermal, Pressure and Light Induced Spin Transition in the Two-Dimensional Coordination Polymer [Fe(pmd)2[Cu(CN)2]2]

2008

[EN] A complete structural, calorimetric, and magnetic characterisation of the 2D coordination spin crossover polymer {Fe(pmd)(2)[Cu(CN)(2)](2)} is reported. The crystal structure has been investigated below room temperature at 180 K and 90 K, and at 30 K after irradiating the sample at low temperature with green light ( lambda = 532 nm). The volume cell contraction through the thermal spin transition is only 18 angstrom(3) which is lower than the usually observed value of around 25-30 angstrom(3) while the average Fe-N bond distances decrease by the typical value of about 0.19 angstrom. The structural data of the irradiated state indicate that the high spin state is well induced since the …

chemistry.chemical_classificationSpin statesCondensed matter physicsCoordination polymerSpin transitionThermodynamicsCrystal structurePolymerInorganic Chemistrychemistry.chemical_compoundchemistrySpin crossoverFISICA APLICADAThermalIrradiation
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