Search results for "SUSTAINABLE CHEMISTRY"

showing 7 items of 17 documents

Palladium Supported on Cross-Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions

2013

Highly cross-linked imidazolium-based materials, obtained by radical oligomerization of bis-vinylimidazolium salts in the presence of 3-mercaptopropyl-modified silica gel, were used as supports for palladium catalysts. Thanks to the high imidazolium loading these materials were able to support a high amount of the metal (10 wt%). Such materials were characterized by several techniques (13C magic angle spinning nuclear magnetic resonance, the Brunauer-Emmett-Teller technique, X-ray photoelectron spectroscopy, and transmission electron microscopy). The palladium catalysts displayed good activity allowing the synthesis of several biphenyl compounds in high yields working with only 0.1 mol% of …

Green chemistryflow chemistryInorganic chemistrychemistry.chemical_elementCatalysisMetalchemistry.chemical_compoundSuzuki reactionMagic angle spinningsustainable chemistry; catalysis flow chemistrysustainable chemistryC C couplingSuzuki-Miyaura reactioncatalyst recyclingBiphenylcatalysisSilica gelSettore CHIM/06 - Chimica OrganicaGeneral ChemistrypalladiumSuzuki–Miyaura reactionchemistryvisual_artvisual_art.visual_art_mediumC-C couplingPalladiumAdvanced Synthesis & Catalysis
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Luminescence and Light‐Driven Energy and Electron Transfer from an Exceptionally Long‐Lived Excited State of a Non‐Innocent Chromium(III) Complex

2019

Abstract Photoactive metal complexes employing Earth‐abundant metal ions are a key to sustainable photophysical and photochemical applications. We exploit the effects of an inversion center and ligand non‐innocence to tune the luminescence and photochemistry of the excited state of the [CrN6] chromophore [Cr(tpe)2]3+ with close to octahedral symmetry (tpe=1,1,1‐tris(pyrid‐2‐yl)ethane). [Cr(tpe)2]3+ exhibits the longest luminescence lifetime (τ=4500 μs) reported up to date for a molecular polypyridyl chromium(III) complex together with a very high luminescence quantum yield of Φ=8.2 % at room temperature in fluid solution. Furthermore, the tpe ligands in [Cr(tpe)2]3+ are redox non‐innocent, …

LuminescenceMaterials sciencePhotoredox chemistryQuantum yieldSustainable Chemistry010402 general chemistryPhotochemistryLaporte's rule01 natural sciencesCatalysischemistry.chemical_compoundBipyridineElectron transferPhotochemistry | Very Important PaperResearch Articles010405 organic chemistryLigandGeneral MedicineGeneral ChemistryChromophoreAzulene0104 chemical scienceschemistryExcited stateEarth-abundant metalsLuminescenceResearch ArticleAngewandte Chemie International Edition
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Gold recycling at laboratory scale: from nanowaste to nanospheres

2019

The market for products based on nanotechnology, and with it the use of nanomaterials and the generation of nanowaste, increases day by day. Among the vast variety of nanomaterials available, gold nanoparticles (AuNPs) are among the most studied and applied in commercial products. This current situation requires both the development of recovery methods to reduce the amount of nanowaste produced, and new synthetic methods that allow the reuse of recovered gold for new nanomaterial production, keeping in mind both economical and ecological considerations. In this work, a methodology to recover gold from aqueous laboratory nanowaste and transform it into an aqueous HAuCl4 solution was develope…

Materials scienceGeneral Chemical EngineeringNanotechnology02 engineering and technologyNANOWASTELaboratory scaleReuse010402 general chemistry01 natural sciencesRECYCLING CYCLENanomaterialsRecovery method//purl.org/becyt/ford/2.10 [https]Environmental ChemistryGeneral Materials ScienceGREEN CHEMISTRYAqueous solution021001 nanoscience & nanotechnology0104 chemical sciencesGeneral Energy//purl.org/becyt/ford/2 [https]Colloidal goldReagentSUSTAINABLE CHEMISTRYGOLD NANOPARTICLES0210 nano-technology
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Electrifying Organic Synthesis

2018

Abstract The direct synthetic organic use of electricity is currently experiencing a renaissance. More synthetically oriented laboratories working in this area are exploiting both novel and more traditional concepts, paving the way to broader applications of this niche technology. As only electrons serve as reagents, the generation of reagent waste is efficiently avoided. Moreover, stoichiometric reagents can be regenerated and allow a transformation to be conducted in an electrocatalytic fashion. However, the application of electroorganic transformations is more than minimizing the waste footprint, it rather gives rise to inherently safe processes, reduces the number of steps of many synth…

Reaction conditionsoxidation010405 organic chemistrybusiness.industryComputer scienceReviewsThe RenaissancereductionReviewGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundTerminal (electronics)chemistryElectrochemistrysynthetic methodssustainable chemistryOrganic synthesisBiochemical engineeringElectricitybusinessRenewable resourceAngewandte Chemie International Edition
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SWEET IONIC LIQUIDS BASED MATERIALS FOR ENVIRONMENTAL APPLICATIONS

Settore CHIM/06 - Chimica OrganicaIonic Liquids Sustainable Chemistry Ionic Liquid Gels Desulfurisation Energy storage Thermochromism Polymeric film
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Synthesis of vanillin in water by TiO2 photocatalysis

2012

Abstract The photoproduction of vanillin is studied in aqueous medium starting from trans-ferulic acid, isoeugenol, eugenol or vanillyl alcohol by using both commercial and home prepared TiO2 samples as photocatalysts and batch Pyrex photoreactors. The photo-oxidation at room temperature of these compounds produces vanillin with a selectivity ranging from 1.4 to 21 mol% with respect to the converted substrate. An investigation on the intermediates was performed in the case of trans-ferulic acid; for this substrate the most important intermediates were homovanillic acid, vanillyl mandelic acid, trans-caffeic acid, formic acid, acetic acid, and oxalic acid. The carbon mass balance, including …

Titanium dioxide Photocatalysis Vanillin Partial oxidationSettore ING-IND/24 - Principi Di Ingegneria ChimicaChemistryFormic acidSettore ING-IND/25 - Impianti ChimiciTITANIUM DIOXIDEProcess Chemistry and TechnologyVanillinOxalic acidSubstrate (chemistry)Catalysischemistry.chemical_compoundVanillyl alcoholIsoeugenolAcetic acidSUSTAINABLE CHEMISTRYOrganic chemistryVANILLINSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePHOTOCATALYSISSelectivityTiO2 Selective oxidation VanillinGREEN CHEMISTRYGeneral Environmental ScienceApplied Catalysis B: Environmental
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Task-Specific Organic Salts and Ionic Liquids Binary Mixtures: A Combination to Obtain 5-Hydroxymethylfurfural From Carbohydrates

2019

The increase in energy demand and depletion of fossil fuels are among major issues of modern society. Valorization and transformation of raw materials in products of industrial value represents a challenge. This justifies the growing interest of scientific research towards the identification of suitable media and methodologies able to pursue above goals, paying attention to matter of sustainability. On this subject, we studied sulfonic-acid functionalized diimidazolium salts as catalysts for the conversion of fructose and sucrose to 5-hydroxymethylfurfural (5-HMF) in an ionic liquid mixture. In general, using these salts allowed us to obtain 5-HMF in good yields from both substrates in mild…

task-specific organic saltsGreen chemistryCarbohydrate conversionSalt (chemistry)02 engineering and technologyRaw materialSulfonic acidIonic liquid010402 general chemistry01 natural sciences5-HMFCatalysislcsh:Chemistryionic liquidschemistry.chemical_compoundOrganic chemistryReactivity (chemistry)Sustainable chemistryOriginal Researchchemistry.chemical_classification5-hydroxymethylfurfuralTask Specific Ionic LiquidBiomass conversionChemistryGeneral ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnologyTask-specific organic salt0104 chemical sciencesChemistryHammett acidity functionlcsh:QD1-999Ionic liquid0210 nano-technology
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