Search results for "Green Chemistry"

showing 10 items of 159 documents

Photocatalytic Partial Oxidation of 5‐Hydroxymethylfurfural (HMF) to 2,5‐Diformylfuran (DFF) Over a Covalent Triazine Framework in Water

2020

Green chemistrychemistry.chemical_compoundChemistryCovalent bond5-hydroxymethylfurfuralOrganic ChemistryPhotocatalysisOrganic chemistryPartial oxidationPhysical and Theoretical ChemistryHydroxymethylfurfuralAnalytical ChemistryTriazineChemPhotoChem
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Dehydrogenative Anodic Cyanation Reaction of Phenols in Benzylic Positions

2019

Green chemistrychemistry.chemical_compoundChemistryElectrochemistryOrganic chemistryPhenolsCyanationElectrochemistryCatalysisAnodeChemElectroChem
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Evaluation of Antiradical Activity and Reducing Capacity of Synthesised Bispyridinium Dibromides Obtained by Quaternisation of 4-Pyridyl-1,4-dihydrop…

2015

New bispyridinium dibromides based on the 1,4-dihydropyridine (1,4-DHP) cycle were synthesised in the reaction between 4-pyridyl-1,4-DHP derivatives and propargyl bromide. It has been shown that variation of the substituent position on the pyridine as well as small changes in the electronic nature of the 1,4-DHP cycle as a result of the substituent nature at the 3 and 5 positions do not affect the course of the reaction and in all cases the corresponding bispyridinium dibromides 4a–e were formed. The antiradical activity, using 1,1-diphenyl-2-picrylhydrazine as a free radical scavenger, and the reducing capacity using phosphomolybdenum complexes have been evaluated for the newly synthesise…

Green chemistrychemistry.chemical_compoundReaction mechanismchemistryBiocatalysisPyridineSubstituentSupramolecular chemistryOrganic chemistryGeneral ChemistryPropargyl bromideFree radical scavengerMedicinal chemistryAustralian Journal of Chemistry
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Frontispiece: A Novel Cathode Material for Cathodic Dehalogenation of 1,1‐Dibromo Cyclopropane Derivatives

2015

Green chemistrychemistry.chemical_compoundchemistryCathode materialOrganic ChemistryInorganic chemistryOrganic chemistryHalogenationGeneral ChemistryCatalysisCyclopropaneCathodic protectionChemistry – A European Journal
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Metal‐Free Twofold Electrochemical C−H Amination of Activated Arenes: Application to Medicinally Relevant Precursor Synthesis

2020

Abstract The efficient production of many medicinally or synthetically important starting materials suffers from wasteful or toxic precursors for the synthesis. In particular, the aromatic non‐protected primary amine function represents a versatile synthetic precursor, but its synthesis typically requires toxic oxidizing agents and transition metal catalysts. The twofold electrochemical amination of activated benzene derivatives via Zincke intermediates provides an alternative sustainable strategy for the formation of new C−N bonds of high synthetic value. As a proof of concept, we use our approach to generate a benzoxazinone scaffold that gained attention as a starting structure against ca…

Green chemistrydrug scaffoldPrimary (chemistry)Full Paper010405 organic chemistryChemistrybenzoxazinoneOrganic ChemistryGeneral ChemistryFull Papers010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysiselectrochemistrytwofold aminationMetal freeOxidizing agentsustainable chemistryAmine gas treatingSynthetic MethodsAminationChemistry – A European Journal
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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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Green Synthesis, Molecular Characterization and Associative Behavior of Some Gemini Surfactants without a Spacer Group.

2013

A series of new gemini surfactants without a spacer group, disodium 2,3-dialkyl-1,2,3,4-butanetetracarboxylates, were synthesized in a green chemistry context minimizing the use of organic solvents and applying microwaves (MW) when activation energy was required. Once the desired architecture was confirmed by means of the nuclear magnetic resonance technique (1H-NMR, 1H-1H COSY) for all the studied surfactants, the critical micellization concentration was determined by conductance measurements. The diffusion coefficient of micelles formed by the four compounds was characterized using pulsed field gradient (PFG)-NMR. Diffusion coefficients were found to be dependent on the concentration and …

Green chemistrygemini surfactantsmicrowavecritical micelle concentrationDiffusionContext (language use)cosmetic detergentlcsh:TechnologyMicelleArticlegreen synthesigemini surfactants green synthesis microwave cosmetic detergents critical micelle concentration PFG-NMR diffusion coefficientOrganic chemistryMoleculeGeneral Materials Sciencediffusion coefficientlcsh:MicroscopyAlkyllcsh:QC120-168.85Settore CHIM/02 - Chimica Fisicachemistry.chemical_classificationgemini surfactantcosmetic detergentslcsh:QH201-278.5lcsh:TChemistrygreen synthesisChemical engineeringlcsh:TA1-2040Critical micelle concentrationPFG-NMRlcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineeringlcsh:Engineering (General). Civil engineering (General)Pulsed field gradientlcsh:TK1-9971gemini surfactants; green synthesis; microwave; cosmetic detergents; critical micelle concentration; PFG-NMR; diffusion coefficientMaterials (Basel, Switzerland)
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An E-Factor Minimized Protocol for a Sustainable and Efficient Heck Reaction in Flow

2014

A highly sustainable and waste-minimized protocol for Heck coupling has been defined. Optimal conditions have been defined by exploiting a heterogeneous catalyst based on supported ionic liquid-like phases featuring high Pd loading (10 wt %) and by optimizing its efficiency in a recoverable green reaction medium (acetonitrile/water azeotrope). Pure products 4a–l and 6a–h have been isolated chromatography-free in high yields (74–99%) and with extremely low environmental factor (E-factor) values (2.3–5.0). With the application of flow technology, the selected heterogeneous base and Pd catalyst have been fully recovered and reused, and minimum palladium leaching allowed for isolation of the fi…

Green chemistrygreen chemistryRenewable Energy Sustainability and the EnvironmentChemistryGeneral Chemical Engineeringchemistry.chemical_elementcross-coupling. palladiumSettore CHIM/06 - Chimica OrganicaGeneral ChemistryFlow chemistryHeterogeneous catalysisCatalysischemistry.chemical_compoundChemical engineeringHeck reactioncontinuous flowEnvironmental ChemistryOrganic chemistryLeaching (metallurgy)C-C couplingAcetonitrilecross-coupling. palladium green chemistryPalladiumPalladiumACS Sustainable Chemistry & Engineering
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Recyclable heterogeneous palladium catalysts in pure water: sustainable developments in Suzuki, Heck, Sonogashira and Tsuji-Trost reactions

2010

This review summarizes the progress made essentially these last ten years on heterogeneous palladium catalysis in pure water. The work covers four important palladium-catalyzed transformations for carbon-carbon bond formation: Suzuki, Heck, Sonogashira and Tsuji-Trost reactions. The discussion focuses on the efficiency and reusability of the heterogeneous catalysts as well as on the experimental conditions from a sustainable chemistry point of view. The review is introduced by a discussion on mechanistic aspects inherent to heterogeneous catalysis.

Green chemistryheterogeneous palladium catalysts010405 organic chemistrywaterSonogashira couplingchemistry.chemical_elementGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energySuzuki reaction -Tsuji-Trost reaction0104 chemical sciencesCatalysisTsuji–Trost reaction[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactionchemistrySuzuki reactionHeck reactionOrganic chemistrySonogashira reactionComputingMilieux_MISCELLANEOUSPalladium
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Structural insight on organosilica electrodes for waste-free alcohol oxidations

2007

Organic modification of sol-gel catalytic glassy electrodes made of a thin layer of organosilica doped with nitroxyl radical TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) crucially enhances stability in the waste-free oxidation of alcohols to carbonyls in water. Structural comparison between analogous films made of organosilica and unmodified SiO2 shows that the origin of the pronounced stable activity of the ORMOSIL film lies in high hydrophobic and also in the pronounced low degree of hydrophilicity.

Green chemistryoxidationalcoholgreen chemistryInorganic chemistryAlcoholNitroxylGeneral ChemistryPhotochemistryHeterogeneous catalysisOrmosilCatalysisCatalysischemistry.chemical_compoundchemistryAlcohol oxidationsol-gelanodicTEMPOSol-gel
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