Search results for ":QUÍMICA [UNESCO]"

showing 10 items of 49 documents

Diels-Alder reaction between indoles and cyclohexadienes photocatalyzed by a (thia)pyrylium salt

2007

"Thiapyrylium salt 1 is an efficient photocatalyst in the Diels-Alder reaction between indoles (InHs) and 1,3-cyclohexadienes (CHDs). For instance, irradiation of deaerated dichloromethane solutions containing 1 (1 mM), indole (20 mM) and cyclohexadiene (40 mM), in the presence of an acylating agent, led to the Diels-Alder cycloadduct in 62% yield (endo:exo ratio of 1.8:1). Taking into account the very high intersystem crossing yield (Φisc = 0.97) of thiapyrylium salt 1, involvement of its triplet excited state in this Diels-Alder reaction has been studied using steadystate and time-resolved experiments; the results are compared with those previously obtained for pyrylium salts, which exhib…

Indoles 1.3-cyclohexadienesUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Diels-Alder reaction ; Photocatalysis ; Thiapyrylium salts ; Indoles 1.3-cyclohexadienesUNESCO::QUÍMICA::Química orgánicaPhotocatalysisDiels-Alder reaction:QUÍMICA [UNESCO]Thiapyrylium salts
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Stereodifferentiation in the formation and decay of the encounter complex in bimolecular electron transfer with photoactivated acceptors.

2005

Experimental evidence has been obtained for the involvement of encounter complexes between both enantiomers of a π,π* triplet excited ketone and a chiral phenol or indole. Determination of the pre-equilibrium constants (KEC) and the intrinsic decay rate constants (kd) indicates a significant stereodifferentiation in both steps of the quenching process. Perez Prieto, Julia, Julia.Perez@uv.es ; Galian, Raquel Eugenia, Raquel.Galian@uv.es ; Morant Miñana, Maria Carmen, Maica.Morant@uv.es

KetoneFormation and decayUNESCO::QUÍMICAPhotochemistry:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundElectron transferBimolecular electronReaction rate constantMaterials ChemistryPhenolUNESCO::QUÍMICA::Química orgánicaStereodifferentiatioPhotoactivated acceptorschemistry.chemical_classificationIndole testQuenching (fluorescence):QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryExcited statePhotoactivated acceptors ; Bimolecular electron ; Stereodifferentiatio ; Formation and decayCeramics and CompositesEnantiomerChemical communications (Cambridge, England)
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Triazolopyridines 22.1 Description of new 7,9-di(2-pyridyl)[1,2,3]triazolo[5',1':6,1]pyrido[3,2-d]pyrimidines

2002

The new heteroaromatic compounds, 7,9-di(2-pyridyl)[1,2,3]triazolo[5',1':6,1]pyrido[3,2-d] pyrimidines 11a-c, were synthesized in two steps from readily available triazolopyridines 1a-c. Regioselective lithiation of 1a-c followed by treatment with 2-cyanopyridine gave a mixture of compounds 5a-c, and 11a-c in moderate to low yields, together with gums. Similar reactions with the triazolopyridine 1d gave as the only identified compound the triazolopyridine derivative 5d. Abarca Gonzalez, Belen, Belen.Abarca@uv.es ; Ballesteros Campos, Rafael, Rafael.Ballesteros@uv.es ; Chadlaoui, Mimoun, michad@alumni.uv.es

LithiationUNESCO::QUÍMICANitrogen heterocycles:QUÍMICA::Química orgánica [UNESCO]UNESCO::QUÍMICA::Química orgánicaHelicating ligands:QUÍMICA [UNESCO]Nitrogen heterocycles ; Helicating ligands ; Lithiation
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Tuning the pore size from micro- to meso-porous in thermally stable aluminophosphates

1999

Thermally stable porous aluminophosphates (ICMUV-3) with P/Al molar ratios in the range 0.15 <= P/Al <= 0.75 and showing continuously adjustable pore sizes from 13 to 37 Å have been prepared through a surfactant-assisted procedure without changing the surfactant length and/or addition of organic expansors. Cabrera Medina, Saul, Saul.Cabrera@uv.es ; El Haskouri, Jamal, Jamal.Haskouri@uv.es ; Beltran Porter, Aurelio, Aurelio.Beltran@uv.es ; Beltran Porter, Daniel, Daniel.Beltran@uv.es ; Amoros del Toro, Pedro Jose, Pedro.Amoros@uv.es

Pore sizeRange (particle radiation)Materials scienceAluminophosphatesUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysMineralogyMeso-porousGeneral Chemistry:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAluminophosphates ; Micro-porous ; Meso-porous ; Organic expansorsPulmonary surfactantChemical engineeringOrganic expansorsMicro-porousMaterials ChemistryCeramics and CompositesUNESCO::QUÍMICA::Química orgánicaPorosity
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Triazolopyridines 23.1 Synthesis of 5,5'-bi[1,2,3]triazolo[5,1-a]isoquinoline

2004

5,5'-Bi[1,2,3]triazolo[5,1-a]isoquinoline 6 has been synthesised from [1,2,3]triazolo[5,1-a] isoquinoline 5 by four procedures, dimerisation by LDA, Stille and Suzuki self-coupling reactions, and Suzuki cross-coupling reaction. The last is the best. Compound 6 gives 1,1'- bi(acetoxymethyl)-3,3'-biisoquinoline 10 by triazolo ring opening by acetic acid. Abarca Gonzalez, Belen, Belen.Abarca@uv.es ; Ballesteros Campos, Rafael, Rafael.Ballesteros@uv.es ; Gay Roig, Bernat, bergay@alumni.uv.es

Self-coupling and cross-coupling reactionsBitriazoloisoquinolines ; Triazoloisoquinolines ; Lithiation reaction ; Self-coupling and cross-coupling reactionsUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Lithiation reactionUNESCO::QUÍMICA::Química orgánicaBitriazoloisoquinolinesTriazoloisoquinolines:QUÍMICA [UNESCO]
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State selective electron injection in non-aggregated titanium phthalocyanine sensitised nanocrystalline TiO2 films

2004

We describe a novel titanium phthalocyanine that shows no aggregation when anchored to nanocrystalline TiO2 films through its axial carboxylated ligand without the use of co-adsorbents; state selective electron injection into the TiO2 is demonstrated, resulting in efficient photocurrent generation in dye sensitised photoelectrochemical solar cells. Palomares Gil, Emilio J, epagil@alumni.uv.es

Solar cellsMaterials scienceState selectiveUNESCO::QUÍMICAchemistry.chemical_elementNanotechnologyPhotochemistry:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundElectron injectionMaterials ChemistryUNESCO::QUÍMICA::Química orgánicaElectron injectionPhotocurrentTitaniumLigand:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryNanocrystalline materialSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryTiO2 filmsCeramics and CompositesPhthalocyanineElectron injection ; Titanium ; TiO2 films ; Solar cellsTitanium
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Polyamines containing naphthyl groups as pH-regulated molecular machines driven by light

2001

A series of compounds made up by linking methylnaphthalene fragments at both ends of different polyamine chains have shown to behave as pH-regulated molecular machines driven by light and fluorescence emission studies have proved the formation of an excimer between the two naphthalene units whose appearance, fluorescence intensity and decay times depend on the pH value of the media. Albelda Gimeno, Maria Teresa, Teresa.Albelda@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es ; Soriano Soto, Concepción, Concepcion.Soriano@uv.es

StereochemistryPHUNESCO::QUÍMICAPhotochemistryExcimerNaphthyl:QUÍMICA [UNESCO]CatalysisFluorescencechemistry.chemical_compoundMaterials ChemistryPolyaminesUNESCO::QUÍMICA::Química orgánicaMethylnaphthaleneNaphthalene:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryFluorescenceMolecular machineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFluorescence intensitychemistryPolyamines ; Naphthyl ; Methylnaphthalene ; PH ; FluorescenceCeramics and CompositesPolyamine
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Unit 2. Stereochemistry

2018

Este documento ha sido elaborado en el marco de un proyecto de Renovación de Metodologías Docentes concedido por el Servicio de Formación Permanente de la Universitat de València (Código de la solicitud: UV-SFPIE_RMD17-725369). Este documento forma parte de la asignatura "Química Orgánica Avanzada" impartida en el "Máster Universitario en Química" This document is part of the course "Advanced Organic Chemistry" of the Master's Degree in Chemistry of the University of Valencia

StereochemistryUNESCO::QUÍMICA::Química orgánica ::Estereoquímica y análisis conformacionalOrganic Chemistry
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Synthetic and theoretical studies of novel ring closure and ring opening reactions

2006

Ring closure and ring opening reactions are in many cases useful synthetic procedures in organic chemistry. They allow the preparation of complex molecules with high stereoselectivity and good yields. Mechanistic and theoretical studies have been carried out on the transformation of 2-aminopyrimidines into imidazo[1,2-c]pyrimidines and guanidines, respectively, through ring closure and ring opening reactions, as well as the transamidation reactions through the ring closure and ring opening of guanidine derivatives, which constitute novel synthetic methods. Sepulveda Arques, Jose, Jose.Sepulveda@uv.es

Transamidation reactionUNESCO::QUÍMICAMichael addition:QUÍMICA::Química orgánica [UNESCO]Ring openingUNESCO::QUÍMICA::Química orgánicaImidazopyrimidines ; Guanidines ; Michael addition ; Ring closure ; Ring opening ; Transamidation reactionGuanidines:QUÍMICA [UNESCO]Ring closureImidazopyrimidines
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Triazolopyridines 21.1 The stereochemistry of 1-[1,2,3]triazolo [1,5-a] pyridin-7-yl-4-(2h-[1,2,3]triazol-4-yl)-1,3-butadienes and triazolo ring open…

2002

The synthesis and NMR study of the geometry of 1-[1,2,3]triazolo[1,5-a]pyridin-7-yl-4-(2H- [1,2,3]triazol-4-yl)-1,3-butadienes 1a, 1b, 5 and of new 1-(6-substituted-2-pyridyl)-4-(2H- [1,2,3]triazol-4-yl)-1,3-butadienes 8-10 is reported. The stereochemistry of all butadienes studied is 1E, 3E except for compound 5 that is the 1Z, 3Z stereoisomer of 1a. Abarca Gonzalez, Belen, Belen.Abarca@uv.es ; Ballesteros Campos, Rafael, Rafael.Ballesteros@uv.es

Triazolopyridines ; Alkenes ; Stereochemistry determinationStereochemistry determinationUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]TriazolopyridinesUNESCO::QUÍMICA::Química orgánicaAlkenes:QUÍMICA [UNESCO]
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