Search results for "visible-light"

showing 10 items of 13 documents

9,10-Phenanthrenedione as Visible-Light Photoredox Catalyst: A Green Methodology for the Functionalization of 3,4-Dihydro-1,4-Benzoxazin-2- Ones thro…

2018

A visible-light photoredox functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones through a Friedel-Crafts reaction with indoles using an inexpensive organophotoredox catalyst is described. The reaction uses a dual catalytic system that is formed by a photocatalyst simple and cheap, 9,10-phenanthrenedione, and a Lewis acid, Zn(OTf)2. 5W white LEDs are used as visible-light source and oxygen from air as a terminal oxidant, obtaining the corresponding products with good yields. The reaction can be extended to other electron-rich arenes. Our methodology represents one of the most valuable and sustainable approach for the functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones, as compared to th…

010402 general chemistrylcsh:Chemical technology01 natural sciencesCatalysisCatalysislcsh:Chemistrychemistry.chemical_compoundCatàlisiTryptophollcsh:TP1-1185Lewis acids and basesorganic_chemistryPhysical and Theoretical ChemistryFriedel-Crafts reactionFriedel–Crafts reaction010405 organic chemistryindolesCombinatorial chemistry0104 chemical scienceschemistrylcsh:QD1-999visible-light photocatalysis14-benzoxazin-2-onesPhotocatalysisSurface modificationorganophotoredox catalysisQuímica orgànicaDerivative (chemistry)Visible spectrum
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Microscopic Revelation of Charge-Trapping Sites in Polymeric Carbon Nitrides for Enhanced Photocatalytic Activity by Correlating with Chemical and El…

2019

The influences of chemical and electronic structures on the photophysical properties of polymeric carbon nitrides (PCNs) photocatalysts, which govern the microscopic mechanisms of the superior photocatalytic activity under visible-light irradiation, have been resolved in this work. Time-resolved photoluminescence and in situ electron paramagnetic resonance measurements indicate that the photoexcited electrons in the fractured PCNs swiftly transfer to the C2p-localized states where the trapped photoelectrons exhibit longer lifetime compared to those in the ordinary PCNs. Moreover, the structure deviation at the carbon (Cb) atoms around the bridging sites of heptazine ring units, where trappe…

021110 strategic defence & security studiesMaterials sciencePhotoluminescenceHeptazineHydrogen bond0211 other engineering and technologiesDFT calculation02 engineering and technologyElectronPhotoelectric effect021001 nanoscience & nanotechnologyPhotochemistrylaw.inventionpolymeric carbon nitridechemistry.chemical_compoundchemistrylawSSNMR spectroscopyPhotocatalysisGeneral Materials ScienceDensity functional theoryvisible-light-driven photocatalyst0210 nano-technologyElectron paramagnetic resonanceEPR spectroscopyACS Applied Materials & Interfaces
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Multi-doped Brookite-Prevalent TiO2 Photocatalyst with Enhanced Activity in the Visible Light

2018

© 2018 Springer Science+Business Media, LLC, part of Springer Nature Abstract: Enabling solar and/or visible light-driven photocatalysis is a crucial step to access innovative applications in environmental science and sustainable energy. Titanium dioxide is the most used photocatalyst because of its low cost and toxicity, however it is also limitedly active under visible light irradiation due to its wide band gap. Among its polymorphs, brookite holds promising optoelectronic properties for visible light photocatalysis, which have to the best of our knowledge been limitedly exploited. Here, a C,S,N-doped brookite-based TiO2has been prepared via a rapid one-pot sol–gel synthesis. Besides subs…

Band gap02 engineering and technology010402 general chemistry01 natural sciencesCatalysisHeterogeneous catalysichemistry.chemical_compoundVisible-light photocatalysiSpecific surface areaBrookiteDopingHeterogeneous catalysisbusiness.industryBrookiteDopingWide-bandgap semiconductorGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesVisible-light photocatalysischemistryvisual_artTitanium dioxidePhotocatalysisvisual_art.visual_art_mediumOptoelectronicsTitanium dioxide0210 nano-technologybusinessVisible spectrum
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Tuning Azoheteroarene Photoswitch Performance through Heteroaryl Design

2017

International audience; Photoswitchable compounds, which can be reversibly switched between two isomers by light, continue to attract significant attention for a wide array of applications. Azoheteroarenes represent a relatively new but understudied type of photoswitch, where one of the aryl rings from the conventional azobenzene class has been replaced with a five-membered heteroaromatic ring. Initial studies have suggested the azoheteroarenes – the arylazopyrazoles in particular – to have excellent photoswitching properties (quantitative switching and long Z isomer half-life). Here we present a systematic computational and experimental study to elucidate the origin of the long thermal hal…

CHEMICAL-REACTIONSMOLECULAR SWITCHESFUNCTIONAL RESPONSE THEORYChemistry Multidisciplinary010402 general chemistryRing (chemistry)Photochemistry01 natural sciencesBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryAZO-COMPOUNDSPHOTOISOMERIZATION[CHIM]Chemical SciencesTO-TRANS ISOMERIZATIONAZOBENZENEScience & TechnologyPhotoswitch010405 organic chemistryArylSOLAR THERMAL STORAGEGeneral ChemistryCombinatorial chemistry0104 chemical sciencesChemistrychemistryAzobenzenePhysical SciencesEXCITATION-ENERGIESVISIBLE-LIGHT03 Chemical Sciences
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New polymorph of InVO4: A high-pressure structure with six-coordinated vanadium

2013

A new wolframite-type polymorph of InVO4 is identified under compression near 7 GPa by in situ high-pressure (HP) X-ray diffraction (XRD) and Raman spectroscopic investigations on the stable orthorhombic InVO4. The structural transition is accompanied by a large volume collapse (Delta V/V = -14%) and a drastic increase in bulk modulus (from 69 to 168 GPa). Both techniques also show the existence of a third phase coexisting with the low- and high-pressure phases in a limited pressure range close to the transition pressure. XRD studies revealed a highly anisotropic compression in orthorhombic InVO4. In addition, the compressibility becomes nonlinear in the HP polymorph. The volume collapse in…

DiffractionVanadiumchemistry.chemical_elementOrtho-vanadatesInorganic Chemistrysymbols.namesakeThird phaseVisible-light irradiationFormsPhysical and Theoretical ChemistrySpectroscopySpectroscopyBulk modulusCRYSTALChemistryCRVO4TIVO4CrystallographyPhaseFISICA APLICADATransitionCompressibilitysymbolsOrthorhombic crystal systemRaman spectroscopyDiffraction
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Visible-light photoredox catalyzed synthesis of pyrroloisoquinolines via organocatalytic oxidation/[3 + 2] cycloaddition/oxidative aromatization reac…

2014

Beilstein journal of organic chemistry 10, 1233-1238 (2014). doi:10.3762/bjoc.10.122

Lettervisible-lightoxidationphotoredox catalysisPhotochemistryalkaloidsCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryRose bengalOrganic chemistryorganocatalysisIsoquinoline[3 + 2] cycloadditionlcsh:ScienceRose BengalphotochemistryOrganic ChemistryAromatizationPhotoredox catalysisCycloadditionChemistrychemistryOrganocatalysislcsh:QQuímica orgànicaVisible spectrumBeilstein Journal of Organic Chemistry
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Coordination networks incorporating halogen-bond donor sites and azobenzene groups

2016

Two Zn coordination networks, {[Zn(1)(Py)2]2(2-propanol)}n (3) and {[Zn(1)2(Bipy)2](DMF)2}n (4), incorporating halogen-bond (XB) donor sites and azobenzene groups have been synthesized and fully characterized. Obtaining 3 and 4 confirms that it is possible to use a ligand wherein its coordination bond acceptor sites and XB donor sites are on the same molecular scaffold (i.e., an aromatic ring) without interfering with each other. We demonstrate that XBs play a fundamental role in the architectures and properties of the obtained coordination networks. In 3, XBs promote the formation of 2D supramolecular layers, which, by overlapping each other, allow the incorporation of 2-propanol as a gues…

MOF Supramolecular Chemistry Halogen Bonding AzobenzeneStereochemistry116 Chemical sciencesSupramolecular chemistry02 engineering and technology010402 general chemistryRing (chemistry)01 natural sciencesIUPAC RECOMMENDATIONS 2013chemistry.chemical_compoundMETAL-ORGANIC FRAMEWORKSdell'Università e della RicercaCHEMISTRYTO-CRYSTAL ISOMERIZATIONMinistero dell'IstruzioneMoleculeGeneral Materials Scienceta215SUPRAMOLECULAR SYNTHESISHalogen bondMETAL-ORGANIC FRAMEWORKS; IUPAC RECOMMENDATIONS 2013; TO-CRYSTAL ISOMERIZATION; SUPRAMOLECULAR SYNTHESIS; VISIBLE-LIGHT; POLYMERS; FLUOROAZOBENZENES; COCRYSTALS; COMPLEXES; CHEMISTRYLigandChemistryFLUOROAZOBENZENESMinistero dell'Istruzione dell'Università e della RicercaGeneral ChemistryCOCRYSTALS021001 nanoscience & nanotechnologyCondensed Matter PhysicsAcceptor0104 chemical sciencesCrystallographyAzobenzeneMIURMetal-organic frameworkCOMPLEXESSettore CHIM/07 - Fondamenti Chimici Delle TecnologieVISIBLE-LIGHTPOLYMERS0210 nano-technology
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Reversible oxidation of WOx and MoOx nano phases

2012

International audience; WOx and MoOx nano phases were prepared on TiO2(1 1 0) surfaces by a CVD procedure consisting of adsorption and decomposition of W(CO)(6) or Mo(CO)(6) precursors followed by annealing under UHV. Metal amount involved in each elaborated sample is in the fractional range from 0.1 to 0.35 equivalent monolayer (eqML) of W or Mo. Evolution of sample stoichiometry as a function of subsequent treatment is followed by valence band and core level photoemission as well as work function measurement. In each case, exposure of samples to molecular oxygen at room temperature induces an increase of sample work function in a range of several tenth of eV. Such a work function change i…

Materials scienceAnnealing (metallurgy)Inorganic chemistryAnalytical chemistrychemistry.chemical_elementCATALYSTS02 engineering and technologyTungsten010402 general chemistryTIO2(110) SURFACE01 natural sciencesSTOICHIOMETRYCatalysisTUNGSTEN-OXIDE[ CHIM.OTHE ] Chemical Sciences/OtherMonolayerWork functionHEXACARBONYL ADSORPTIONSOL-GELVISIBLE-LIGHT IRRADIATIONTIO2 110MOLYBDENUMGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryMolybdenumPhotocatalysisPHOTOCATALYSIS[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyStoichiometryTitanium
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Photoactivity under visible light of metal loaded TiO2 catalysts prepared by low frequency ultrasound treatment

2017

Abstract Visible-light responsive bare and metal loaded (Pt, Ag, Rh, Pd) TiO 2 photocatalysts were prepared by using a simple ultrasound treatment. This method induced bulk oxygen deficiency resulting in a narrowing bandgap (from 3.18 to 3.04 eV) and in visible light absorption. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), BET specific surface area (SSA) and pore size distribution (PSD), UV–vis diffuse reflectance spectroscopy (DRS), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity of the samples was evaluated by using the 4-nitrophenol oxidation reaction and the photocatalytic oxidation of glucose w…

Materials scienceDiffuse reflectance infrared fourier transformScanning electron microscopeAnalytical chemistryUltrasound treatment02 engineering and technology010402 general chemistry01 natural sciencesCatalysisCatalysisymbols.namesakeMetal loaded TiO2X-ray photoelectron spectroscopySpecific surface areaAbsorption (electromagnetic radiation)Chemistry (all)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesVisible-light active TiO2PhotocatalysissymbolsSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyRaman spectroscopyValence band edge shiftVisible spectrum
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Modification of Nanocrystalline WO3 with a Dicationic Perylene Bisimide: Applications to Molecular Level Solar Water Splitting

2015

[(N,N?-Bis(2-(trimethylammonium)ethylene) perylene 3,4,9,10-tetracarboxylic acid bisimide)(PF6)2] (1) was observed to spontaneously adsorb on nanocrystalline WO3 surfaces via aggregation/hydrophobic forces. Under visible irradiation (? > 435 nm), the excited state of 1 underwent oxidative quenching by electron injection (kinj > 108 s-1) to WO3, leaving a strongly positive hole (Eox ? 1.7 V vs SCE), which allows to drive demanding photo-oxidation reactions in photoelectrochemical cells (PECs). The casting of IrO2 nanoparticles (NPs), acting as water oxidation catalysts (WOCs) on the sensitized electrodes, led to a 4-fold enhancement in photoanodic current, consistent with hole transfer from …

Models MolecularMolecular ConformationNanoparticleImidesPhotochemistryBiochemistryTungstenCatalysisNOCatalysiElectron Transportchemistry.chemical_compoundColloid and Surface ChemistryTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYWO3ComputingMethodologies_SYMBOLICANDALGEBRAICMANIPULATIONperylenePhotoelectrochemical cellIrO2Quenching (fluorescence)Chemistry (all)charge transferWaterOxidesGeneral ChemistryPhotoelectrochemical cellPhotochemical ProcessesSolar fuelChemistry (all); Catalysis; Biochemistry; Colloid and Surface ChemistryNanocrystalline materialperylene WO3 charge transfer IrO2MicrosecondchemistryWater SplittingSunlightVISIBLE-LIGHT; ARTIFICIAL PHOTOSYNTHESIS; PHOTOELECTROCHEMICAL CELL; OXIDATION CATALYSTS; ELECTRON-TRANSFER; FABRICATIONNanoparticlesPerylene bisimideWater splittingPeryleneMathematicsofComputing_DISCRETEMATHEMATICS
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