Search results for "electronics"

showing 10 items of 4340 documents

Reversible Digital And Holographic Optical Storafe In Polymeric Liquid Crystals (PLC)

1987

A new reversible optical storage technique based on azo dye containing liquid crystalline polymers and copolymers is described. Monodomain films of the polymers were used as storage medium. Digital and holographic information was stored and reconstructed. The stored information can be erased and the writing process is repeatable. The storage process is explained in terms of a transcis isomerization of the mesogen inducing local director field distortions.

chemistry.chemical_classification3D optical data storageMaterials sciencebusiness.industryMesogenHolographyPolymerOptical storagelaw.inventionOpticschemistrylawLiquid crystalComputer data storageOptoelectronicsbusinessDigital holographySPIE Proceedings
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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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Synthesis of Highly Substituted Unsymmetrical 1,2-Diamines, 1,2-Diimines, Imidazolium Salts and Imidazolylidenes by Aldimine Cross-Coupling

2007

α-Aminonitriles derived from aromatic aldehydes and primary amines can be deprotonated quantitatively without the use of protecting groups. The 1,2-addition of the resulting stabilized α-aminocarbanions to imines yields α-aminoimines and the tautomeric enediamines. These unstable compounds can directly be oxidized to 1,2-diimines or reduced to 1,2-diamines in a one-pot reaction. 1,2-Diamines can be obtained in high diastereoselectivity by reduction of the 1,2-diimines. In this case, the relative configuration of the products can be chosen depending on the reduction conditions. Cyclization of the unsymmetrical diimines with halomethyl ethers or esters leads to 1,3,4,5-tetrasubstituted imidaz…

chemistry.chemical_classificationAldiminePrimary (chemistry)ChemistryOrganic ChemistryGeneral MedicinePhotochemistryTautomerCatalysisCoupling (electronics)DeprotonationNucleophilePolymer chemistryCarbonyl derivativesCoupling (piping)Synthesis
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Amplified spontaneous emission of glass forming DCM derivatives in PMMA films

2014

4-(dicyanomethylene)-2-methyl- 6-(p-dimethylaminostyryl)-4H-pyran ( DCM ) is well known red laser dye which can be used also in solid state organic lasers. The lowest threshold value of amplified spontaneous emission was achieved by doping 2wt% of DCM molecule in tris-(8-hydroxy quinoline) aluminium (Alq

chemistry.chemical_classificationAmplified spontaneous emissionDye laserMaterials sciencebusiness.industryDopingQuinolinechemistry.chemical_elementPolymerPhotochemistryLaserlaw.inventionchemistry.chemical_compoundchemistryAluminiumlawOptoelectronicsbusinessLuminescenceSPIE Proceedings
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Synthesis of gold nanotubes with variable wall thicknesses

2013

We report the synthesis of gold nanotubes with variable wall thicknesses that is accomplished by the deposition of sacrificial hydrophobic polymer cores followed by gold shells within an anodic aluminum oxide template. We demonstrate that by varying polymer core hydrophobicity, the resulting gold shell thickness can be varied. There are two requirements for gold shell formation: (1) the polymer core must be able to be electrodeposited into a tubular (as opposed to wire-like) structure, and (2) the polymer must be hydrophobic, such that it collapses upon exposure to an aqueous solution. An array of gold nanotubes has variable plasmonic properties and can function as a surface enhanced Raman …

chemistry.chemical_classificationAqueous solutionMaterials scienceRenewable Energy Sustainability and the EnvironmentShell (structure)Core (manufacturing)General ChemistrySubstrate (electronics)PolymerSurface-enhanced Raman spectroscopychemistryGeneral Materials ScienceComposite materialPlasmonDeposition (law)J. Mater. Chem. A
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Cobalt−NHC Catalyzed C(sp 2 )−C(sp 3 ) and C(sp 2 )−C(sp 2 ) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl and Aryl Grignard Reagents

2020

chemistry.chemical_classificationArylOrganic Chemistrychemistry.chemical_elementMedicinal chemistryCatalysisCatalysisInorganic ChemistryCoupling (electronics)chemistry.chemical_compoundchemistryReagentPhysical and Theoretical ChemistryCobaltAlkylChemCatChem
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Inverted Solution Processable OLEDs Using a Metal Oxide as an Electron Injection Contact.

2007

A new type of bottom-emission electroluminescent device is described in which a metal oxide is used as the electron-injecting contact. The preparation of such a device is simple. It consists of the deposition of a thin layer of a metal oxide on top of an indium tin oxide covered glass substrate, followed by the solution processing of the light-emitting layer and subsequently the deposition of a high-workfunction (air-stable) metal anode. This architecture allows for a low-cost electroluminescent device because no rigorous encapsulation is required. Electroluminescence with a high brightness reaching 5700 cd m–2 is observed at voltages as low as 8 V, demonstrating the potential of this new a…

chemistry.chemical_classificationBrightnessMaterials sciencebusiness.industryOxideFísicaPolymerElectroluminescenceCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsIndium tin oxideBiomaterialschemistry.chemical_compoundchemistryElectrochemistryOLEDOptoelectronicsbusinessMaterialsVoltageDiodeAdvanced Functional Materials
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Nickel‐Catalyzed C(sp2)−C(sp3) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl Grignard Reagents

2019

Aryl tosylates are an attractive class of electrophiles for cross‐coupling reactions due to ease of synthesis, low price, and the employment of C−O electrophiles, however, the reactivity of aryl tosylates is low. Herein, we report the Ni‐catalyzed C(sp2)−C(sp3) Kumada cross‐coupling of aryl tosylates with primary and secondary alkyl Grignard reagents. The method delivers valuable alkyl arenes by cross‐coupling with challenging alkyl organometallics possessing β‐hydrogens that are prone to β‐hydride elimination and homo‐coupling. The reaction is catalyzed by an air‐ and moisture stable‐Ni(II) precatalyst. A broad range of electronically‐varied aryl tosylates, including bis‐tosylates, underwe…

chemistry.chemical_classificationC(sp2)−C(sp3) cross-couplingArylchemistry.chemical_elementGeneral ChemistryAlkylationCatalysisCoupling (electronics)chemistry.chemical_compoundNickelnickelchemistryReagentPolymer chemistrycross-couplingKumada cross-couplingalkylationAlkylAdvanced Synthesis & Catalysis
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Diamondoids: functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons

2014

The term “diamondoid” describes cage hydrocarbon molecules that are superimposable on the diamond lattice. Diamondoids that are formally built by face-fusing of adamantane units, namely diamantane, triamantane, tetramantane, etc., have fascinated chemists since the beginning of the last century. The functionalization of these perfectly defined (C,H)-molecules is described here. Thus, diamondoid halides and diamondoid alcohols are first rank precursors for amino and phosphine-substituted diamondoids that have proved to be highly useful in therapeutic applications and metal catalysis, respectively. The extent of functionalization and polyfunctionalization achieved for adamantane and diamantan…

chemistry.chemical_classificationChemistryAdamantaneMolecular electronicsGeneral ChemistryPolymerDiamondoidCatalysischemistry.chemical_compoundComputational chemistryOrganocatalysisMaterials ChemistrySurface modificationMoleculeOrganic chemistryDiamantaneNew J. Chem.
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