Search results for "SUSTAINABLE CHEMISTRY"

showing 10 items of 17 documents

Developments in the dehydrogenative electrochemical synthesis of 3,3′,5,5′-tetramethyl-2,2′-biphenol

2021

Abstract The symmetric biphenol 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol is a well‐known ligand building block and is used in transition‐metal catalysis. In the literature, there are several synthetic routes for the preparation of this exceptional molecule. Herein, the focus is on the sustainable electrochemical synthesis of 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol. A brief overview of the developmental history of this inconspicuous molecule, which is of great interest for technical applications, but has many challenges for its synthesis, is provided. The electro‐organic method is a powerful, sustainable, and efficient alternative to conventional synthesis to obtain this symmetric biphenol up to the …

Green chemistry540 Chemistry and allied sciencespolycycles010405 organic chemistryChemistryoxidationOrganic ChemistryC−C couplingMinireviewsGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesC c couplingelectrochemistry540 Chemiesustainable chemistryMinireviewC−C Coupling | Reviews Showcase
researchProduct

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
researchProduct

Valorisation of industrial iron oxide waste to produce magnetic barium hexaferrite

2016

Barium M-type hexagonal ferrite (BaM, BaFe12O19) is an immensely important magnetic material, which we have successfully made from the simple valorisation of Fe-rich industrial waste from steel wire drawing, with addition of BaCO3 and heating in air to 1000 degrees C. The optimum ratio of Fe. Ba (producing 86 wt% BaM) was found to be 11: 1 (non-stoichiometric), and secondary phases of alpha-Fe2O3 (non-magnetic) and ZnFe2O4 (poorly antiferromagnetic) were always present. This material consisted of small submicron platelets. A hard magnetic ferrite was produced with Ms=48.6 A m(2) kg(-1) and H-c=211.5 kA m(-1). The highest density was achieved by sintering samples with Fe: Ba ratios of 11: 1 …

CeramicsMaterials scienceMagnetic PropertiesFERRITESSettore ING-IND/22 - Scienza e Tecnologia dei MaterialiIron oxideSettore ICAR/10 - Architettura Tecnica02 engineering and technology010402 general chemistrySustainable Chemistry01 natural sciences7. Clean energychemistry.chemical_compoundCeramics; Ferrites; Magnetic Properties; Sustainable Chemistry; Waste preventionFerritesSettore CHIM/03 - Chimica Generale e InorganicaWaste managementMetallurgySettore CHIM/07 - Fondamenti Chimici delle TecnologieGeneral ChemistryBarium hexaferrite021001 nanoscience & nanotechnology0104 chemical sciencesferrite manufacturing building material filler sustainabilitychemistryCERAMICSWaste preventionValorisation0210 nano-technologyWaste prevention
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

Electrochemical synthesis of carbazoles by dehydrogenative coupling reaction

2020

Abstract A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N‐protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.

Green chemistry540 Chemistry and allied sciencesDeblocking filterSupporting electrolyteRadicalSustainable Chemistry010402 general chemistryElectrochemistry01 natural sciencesCatalysisCoupling reactionNC couplingProtecting groupgreen chemistry010405 organic chemistryChemistryCommunicationOrganic Chemistryheterocyclic chemistryGeneral ChemistryCombinatorial chemistryCommunications0104 chemical sciencesAnodecarbazoleselectrochemistry540 Chemie
researchProduct

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
researchProduct

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
researchProduct

22nd International Scientific Conference “EcoBalt 2021”: Book of Abstracts (Riga, Latvia, October 21–23, 2021)

2021

The abstract book contains abstracts of the participants of the 22nd International Scientific Conference "EcoBalt 2021".

Green ChemistryPharmacy and Environment:NATURAL SCIENCES::Chemistry [Research Subject Categories]Environmental EducationEnvironmental ChemistrySustainable Chemistry and New Applied MaterialsAnalytical ChemistryFood safety
researchProduct