Search results for "ELECTROLYTE"

showing 10 items of 746 documents

Effects of primary- and secondary-treated bleached kraft mill effluents on the immune system and physiological parameters of roach.

2000

The present study was designed to examine, whether, effluents from a modern pulp and paper mill using elemental chlorine-free/total chlorine-free (ECF/TCF) bleaching, exert effects on the immune system of fish and, in addition, to relate these findings to physiological parameters known to be affected by bleached kraft-mill effluents (BKME). Roach (Rutilus rutilus) were exposed in laboratory conditions to primary- or secondary-treated effluent from a pulp and paper mill. In order to study their capability to respond to foreign antigens they were immunised with bovine gamma-globulin (BGG) prior to exposure. The number of anti-BGG antibody-secreting cells (ASC) and the number of immunoglobulin…

GillsPaperHydrocortisoneNeutrophilsHealth Toxicology and MutagenesisIndustrial WasteSpleenEnzyme-Linked Immunosorbent AssayFresh WaterAquatic Scienceengineering.materialAndrologyImmune systemAntigenCell MovementmedicineCytochrome P-450 CYP1A1AnimalsLymphocytesRespiratory BurstAdenosine Triphosphatasesbiologybusiness.industryPulp (paper)FishesPaper millWater-Electrolyte Balancebiology.organism_classificationLiver Glycogenmedicine.anatomical_structureImmunoglobulin MImmune SystemImmunologyengineeringOsmoregulationbiology.proteinCarbohydrate MetabolismRutilusAntibodyChlorinebusinessWater Pollutants ChemicalAquatic toxicology (Amsterdam, Netherlands)
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Gold Nanoparticles Coated with a Thermosensitive Hyperbranched Polyelectrolyte: Towards Smart Temperature and pH Nanosensors

2008

GlycerolNanostructureMaterials scienceMolecular StructureTemperatureMetal NanoparticlesNanotechnologyGeneral ChemistryGeneral MedicineHydrogen-Ion ConcentrationCatalysisPolyelectrolyteElectrolytesMicroscopy Electron TransmissionColloidal goldNanosensorGoldMetal nanoparticlesAngewandte Chemie
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New Photosensitive Polymers:  Synthesis and Free Radical Polymerization of Oxypyridinium and Oxyisoquinolinium Functionalized Methacrylate and Styren…

2002

Polymerizable hydroxypyridinium and hydroxyisoquinolinium salts 1a−4a, 2d, and 3d have been prepared from vinylbenzyl chloride or glycidyl methacrylate and 3-hydroxypyridine (2), 4- or 5-hydroxyisoquinoline (1, 3), and 8-hydroxyquinoline (4). Radical homo- and copolymerization with styrene or methyl methacrylate of the salts 1a−3a, 2d, and 3d produced (co)polymers 1e, 2e, 2f, 3f, 1g, 2g, 2h, and 3h. The photosensitive dipolar oxypyridinium or oxyisochinolinium betaine structures were generated in solutions with triethylamine from the low molecular weight and polymeric salt precursors. For the model compounds 1b−4b and (co)polymers 1e, 2e, 2f, 3f, 1g, 2g, 2h, and 3h, the degradation of the l…

Glycidyl methacrylatePolymers and PlasticsOrganic ChemistryRadical polymerizationPhotochemistryMethacrylatePolyelectrolyteStyreneInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateTriethylamineMacromolecules
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Synthesis of Highly Functionalized N , N ‐Diarylamides by an Anodic C, N ‐Coupling Reaction

2019

We report an innovative, sustainable and straightforward protocol for the synthesis of N,N-diarylamides equipped with nonprotected hydroxyl groups by using electrosynthesis. The concept allows the application of various substrates furnishing diarylamides with yields up to 57 % within a single and direct electrolytic protocol. The method is thereby easy to conduct in an undivided cell with constant current conditions offering a versatile and short-cut alternative to conventional pathways.

Green chemistry010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryElectrolyte010402 general chemistryElectrosynthesisElectrochemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reaction0104 chemical sciencesAnodeConstant currentChemistry – A European Journal
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Electrochemical Synthesis of 5-Aryl-phenanthridin-6-one by Dehydrogenative N,C Bond Formation.

2018

Currently, the general synthesis of 5-aryl-phenanthridin-6-ones relies on the involvement of metal catalysis. Despite the urgent demand for green alternatives, avoiding synthetic routes that require transition metals for key roles is still challenging. Electrochemical efforts employing a constant potential protocol in divided cells revealed a possible alternative to the catalytic approach. A constant current protocol, undivided cells, and a remarkably low supporting electrolyte concentration enable a novel access to N-aryl-phenanthridin-6-ones by anodic N,C bond formation using directly generated amidyl radicals. Easy accessible starting materials, a broad scope of applicable functional gro…

Green chemistry010405 organic chemistrySupporting electrolyteArylRadicalOrganic ChemistryGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundTransition metalchemistryvisual_artvisual_art.visual_art_mediumChemistry (Weinheim an der Bergstrasse, Germany)
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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
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A Novel Cathode Material for Cathodic Dehalogenation of 1,1-Dibromo Cyclopropane Derivatives.

2015

Leaded bronze turned out to be an excellent cathode material for the dehalogenation reaction of cyclopropanes without affecting the strained molecular entity. With this particular alloy, beneficial properties of lead cathodes are conserved, whereas the corrosion of cathode is efficiently suppressed. The solvent in the electrolyte determines whether a complete debromination reaction is achieved or if the process can be selectively stopped at the monobromo cyclopropane intermediate. The electroorganic conversion tolerates a variety of functional groups and can be conducted at rather complex substrates like cyclosporine A. This approach allows the sustainable preparation of cyclopropane deriva…

Green chemistryChemistryOrganic ChemistryAlloyInorganic chemistryHalogenationGeneral ChemistryElectrolyteengineering.materialCombinatorial chemistryCatalysisCathodeCyclopropanelaw.inventionCorrosionSolventchemistry.chemical_compoundlawengineeringChemistry (Weinheim an der Bergstrasse, Germany)
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Electrochemical nitration with nitrite

2021

Aromatic nitration has tremendous importance in organic chemistry as nitroaromatic compounds serve as versatile building blocks. This study represents the electrochemical aromatic nitration with NBu4 NO2 , which serves a dual role as supporting electrolyte and as a safe, readily available, and easy-to-handle nitro source. Stoichiometric amounts of 1,1,1-3,3,3-hexafluoroisopropan-2-ol (HFIP) in MeCN significantly increase the yield by solvent control. The reaction mechanism is based on electrochemical oxidation of nitrite to NO2 , which initiates the nitration reaction in a divided electrolysis cell with inexpensive graphite electrodes. Overall, the reaction is demonstrated for 20 examples w…

Green chemistryReaction mechanism540 Chemistry and allied sciencesSupporting electrolyteGeneral Chemical EngineeringElectrochemistryCombinatorial chemistrySolventchemistry.chemical_compoundGeneral EnergychemistryNitrationYield (chemistry)540 ChemieEnvironmental ChemistryGeneral Materials ScienceNitrite
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Sustainable and cost-efficient electro-synthesis of formamidine acetate from cyanamide in aqueous acidic electrolyte

2021

Formamidine represents a versatile building block in synthetic organic chemistry. We developed a new electrochemical synthesis of formamidine acetate by cathodic reduction of cyanamide in an aqueous electrolyte and in high yield. The crude product could be used for further conversions, such as to pyrimidines without purification. Compared to established synthetic routes neither prior processing of cyanamide was necessary, nor precious transition-metal catalyst were required, nor any reagent waste was produced, and only biocompatible and sustainable solvents were employed for this process, following the requirements of green chemistry.

Green chemistrychemistry.chemical_compoundAqueous solutionchemistryReagentYield (chemistry)Environmental ChemistryOrganic chemistryCyanamideElectrolyteElectrochemistryPollutionCatalysisGreen Chemistry
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Electrochemical processes in macro and microfluidic cells for the abatement of chloroacetic acid from water

2014

Abstract The remediation of solutions contaminated with monochloroacetic acid (CAA), which is one of the most resistant haloacetic acids (HAAs) to chemical degradation, dramatically depends on the adopted electrochemical approach: (i) CAA is only poorly oxidized either by homogeneous hydroxyl radical in electro-Fenton (EF), electrogenerated active chlorine or electro-oxidation on Pt anode; (ii) it is moderately abated by direct reduction on silver or compact graphite cathodes (from 30% in macro cells to 60% in the microfluidic devices); (iii) it is quantitatively removed by direct electro-oxidation on a boron-doped diamond (BDD) anode. The use of a microreactor enables operation in the abse…

Haloacetic acidsSupporting electrolyteGeneral Chemical EngineeringInorganic chemistryChloroacetic acidchemistry.chemical_elementElectrochemistryAnodechemistry.chemical_compoundchemistryElectrochemistryChlorinemedicineMicroreactorChemical decompositionmedicine.drugElectrochimica Acta
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