Search results for "Coupling"

showing 10 items of 1862 documents

Performances of the Fault Decoupling Device when unbalanced and multiple faults occur on distribution systems.

2005

Nowadays industrial processes are largely based on electronic devices such as programmable logic controllers and adjustable speed drives. Consequently, industrial equipments became less tolerant towards power supply disturbances. Voltage dips due to faults are surely among the worst disturbances for industrial equipments. A paper machine can be affected by disturbances of only 10% voltage drop lasting for 100 ms. A voltage dip of 75% (of the nominal voltage) with a duration shorter than 100 ms results in material loss in the range of thousands of US Dollars for semiconductors industry [1].

business.product_categorybusiness.industryComputer scienceElectrical engineeringProgrammable logic controllerFault indicatorDistribution systemElectric potentialPaper machineHardware_GENERALControl theoryPower qualitysag detectionElectronicsbusinessVoltage dropDecoupling (electronics)Voltage
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Materiali catalitici a base di nanoparticelle di palladio immobilizzate su nanoforme di carbonio

2019

carbon nanostructurecarbon nanohornpalladium catalysihybrid materialcarbon nanotubeC-C cross-couplingimidazolium salt
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Synthesis of Globular Precursors

2015

o-Carborane (C2 B10 H12 ) was adapted to perform as the core of globular macromolecules, dendrons or dendrimers. To meet this objective, precisely defined substitution patterns of terminal olefin groups on the carborane framework were subjected to Heck cross-coupling reactions or hydroboration leading to hydroxyl terminated arms. These led to new terminal groups (chloro, bromo, and tosyl leaving groups, organic acid, and azide) that permitted ester production, click chemistry, and oxonium ring opening to be performed as examples of reactions that demonstrate the wide possibilities of the globular icosahedral carboranes to produce new dendritic or dendrimer-like structures. Polyanionic speci…

carboranesStereochemistrydendronsOrganic ChemistryGeneral ChemistryCatalysismultibranched compoundsHydroborationchemistry.chemical_compoundpolyanionsNucleophileTosylchemistryDendrimerClick chemistrycross-couplingCarboraneAzideOxonium ionta116Chemistry: A European Journal
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ChemInform Abstract: Polycondensed Nitrogen Heterocycles. Part 22. Pyrrolo(3,4-d)-1,2,3-triazines: A New Ring System as Potential Antineoplastic Agen…

1990

Diazotization of the 3-aminopyrrole-4-carboxamides 6a,b under different conditions directly led to the new ring system pyrrolo[3,4-d]-1,2,3-triazine in excellent yields through an intramolecular coupling reaction. In all the cases it was impossible to isolate the intermediate 3-diazopyrroles.

chemistryIntramolecular forcechemistry.chemical_elementGeneral MedicineRing (chemistry)Medicinal chemistryNitrogenCoupling reactionD-1ChemInform
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ChemInform Abstract: Oxidative (Cross-)Coupling Reactions Mediated by C-H Activation of Thiophene Derivatives by Using Molybdenum(V) Reagents.

2015

The use of MoCl5 renders possible the preparation of various synthetically important polycyclic thienoacenes.

chemistryMolybdenumReagentchemistry.chemical_elementGeneral MedicineOxidative phosphorylationThiophene derivativesCombinatorial chemistryCoupling reactionChemInform
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MoVReagents in Organic Synthesis

2016

The use of MoV reagents, and in particular MoCl5, in organic synthesis is surveyed. The oxidative treatment of aromatic substrates is the most common application. The unique properties of these reagents are due to their high oxidative power combined with exquisite Lewis acid properties. In several examples MoV reagents outperform other common oxidative coupling reagents. C–C bond formation through inter- and intramolecular oxidative coupling can lead to selective formation of five- to eight-membered ring systems. Mechanistic investigations of the courses of reactions involving MoV reagents and aromatic substrates indicate that radical cations are initially formed, entering the oxidative cou…

chemistry.chemical_classification010405 organic chemistryChemistryOrganic ChemistryAlkyne010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundIntramolecular forceReagentOrganic chemistryStereoselectivityOxidative coupling of methaneOrganic synthesisLewis acids and basesPhysical and Theoretical ChemistryIsomerizationEuropean Journal of Organic Chemistry
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New Route to Polynuclear Ni(II) and Cu(II) Complexes with Bridging Oxime Groups That Are Inaccessible by Conventional Preparations

2019

A series of new polynuclear complexes of divalent Ni and Cu with 2-cyano-2-oximino-acetic acid (later AACO2-) were obtained as the result of the ligand modification reaction in the process of complexation, using 2-cyano-2-oximino-acetates such as methyl- (later as MeCO), and ethyl- (as ECO later on). Synthesized compounds were characterized by spectroscopic methods, thermal analysis, magnetochemistry, and X-ray crystallography. Crystal data revealed the formation of the dimeric [Ni(AACO)(H2O)3]2·H2O (1), trimeric K2[Ni3(AACO)4(H2O)4]·4H2O (2), and K2[Cu3(AACO)4(H2O)4]·4H2O (3) complexes, with bridging NO-groups cyanoxime dianions. In the latter two compounds, the AACO2– anions adopt cis-arr…

chemistry.chemical_classification010405 organic chemistryGeneral Chemistry010402 general chemistryCondensed Matter PhysicsOxime01 natural sciencesAntiferromagnetic coupling0104 chemical sciencesDivalentMetalchemistry.chemical_compoundCrystallographychemistryMagnetochemistryvisual_artCrystal datavisual_art.visual_art_mediumGeneral Materials ScienceThermal analysisCrystal Growth & Design
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Synthesis and characterization of new coordination compounds by the use of 2-pyridinemethanol and di- or tricarboxylic acids

2021

The development of synthetic approaches towards new coordination polymers has attracted significant interest due to their fascinating physical properties, as well as their use in a wide range of technological, environmental and biomedical applications. Herein, the initial combination of 2-pyridinemethanol (Hhmp) with 1,4-benzenedicarboxylic acid (H2bdc) or 1,3,5-benzenetricarboxylic acid (H3btc) has been proven a fruitful source of such new species providing access to five new coordination compounds, namely [M2(Hbtc)2(Hhmp)4]·DMF (M = CoII, 1·DMF;NiII, 2·DMF), [Ni(bdc)(Hhmp)2]n·4H2O (3·4H2O), [Zn2(bdc)(hmp)2]n·DMF (4·DMF) and [Fe3(bdc)3(Hhmp)2]n (5). 4·DMF and 5 are the first metal–organic …

chemistry.chemical_classification02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMagnetic susceptibilityAntiferromagnetic coupling0104 chemical sciencesCoordination complexCrystallographychemistrySuperexchangeGeneral Materials Science0210 nano-technologyCrystEngComm
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Nickel‐Mediated Photoreductive Cross Coupling of Carboxylic Acid Derivatives for Ketone Synthesis**

2021

A simple photochemical, nickel-catalyzed synthesis of ketones starting from carboxylic acids is presented. Hantzsch-ester (HE) functions as a cheap, green and strong photoreductant upon visible-light excitation to facilitate radical generation and also engages in the Ni-catalytic cycle to restore the reactive species. With this dual role, HE allows for the coupling of a large variety of radicals (1°,2°, benzylic, α-oxy & α-amino) with aroyl and alkanoyl moieties, a new feature in the synthesis of ketones through dual nickel photoredox catalysis. With both precursors deriving from abundant carboxylic acids, this protocol is a welcome addition to the organic chemistry toolbox. The reactio…

chemistry.chemical_classification540 Chemistry and allied sciencesRadicalCarboxylic acidOrganic ChemistryKetone synthesisCarboxylic AcidsPhotoredox catalysischemistry.chemical_elementGeneral ChemistryKetonesCombinatorial chemistryCatalysisMetalCoupling (electronics)NickelchemistryNickel540 ChemieReagentvisual_artvisual_art.visual_art_mediumPhotocatalysisOxidation-ReductionChemistry – A European Journal
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Evidence for essential primary amino groups in a bacterial coupling factor F1ATPase.

1980

Abstract We have found that the binding of pyridoxal-5′-phosphate to 6 primary amino groups leads to the inactivation of the enzyme. A preferential reaction of pyridoxal-5′-phosphate with the α-subunits of this enzyme can be demonstrated. The reactivity of the amino groups is influenced by various effectors. In the presence of ATP the inhibition of the ATPase activity is noncompetitive.

chemistry.chemical_classificationAdenosine TriphosphatasesPrimary (chemistry)Binding SitesChemistryStereochemistryEffectorCell MembraneBiophysicsCell BiologyBiochemistryMicrococcusCoupling (electronics)Structure-Activity RelationshipEnzymeBiochemistrySolubilityPyridoxal PhosphateAtpase activityReactivity (chemistry)Amino AcidsMolecular BiologyBiochemical and biophysical research communications
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