Search results for "Acceptor"

showing 10 items of 394 documents

Donor–Acceptor Polymers for Electrochemical Supercapacitors: Synthesis, Testing, and Theory

2014

Donor–acceptor polymers can store both a positive and negative charge allowing them to function as both the positive and negative charge storage material in a supercapacitor device, however few have been explored for this application. Here, we describe the synthesis of several donor–acceptor polymers and their electrodeposited polymer electrodes. We use differing molecular structures to examine the effect of electron acceptor concentration and show that device stability can be improved significantly by increasing the acceptor concentration. Further, we provide computational insight into the important chemical requirements for achieving even higher performance supercapacitors based on donor–…

chemistry.chemical_classificationSupercapacitorMaterials scienceNanotechnologyPolymerConjugated systemElectron acceptorAcceptorSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergychemistryElectrochemical supercapacitorsSpecific energyPhysical and Theoretical ChemistryPower densityThe Journal of Physical Chemistry C
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Ternary Polymer Solutions with Hydrogen Bonds, 1

2007

The Flory Huggins methodology coupled to AET has been extended to ternary polymer systems, in particular to solvent (A)/polymer 1 (B)/polymer 2 (C) systems, with the two polymers displaying H-bonding interactions. Because the H-bonding can perturb the randomness of polymeric conformations, the change in Gibbs free energy of mixing, AG, should arise from changes in combinatorial entropy as well as in interaction energy. The combinatorial part of AG is evaluated through AET as a function of the association constant η between B and C components, the autoassociation constant a between B components, and the independent number m of interaction sites of acceptor C. The enthalpic contribution is ev…

chemistry.chemical_classificationTernary numeral systemPolymers and PlasticsChemistryHydrogen bondOrganic ChemistryThermodynamicsInteraction energyPolymerEntropy of mixingFlory–Huggins solution theoryCondensed Matter PhysicsAcceptorInorganic ChemistryMaterials ChemistryTernary operationMacromolecular Theory and Simulations
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Concentration of amino acids using supported liquid membranes with di-2-ethylhexyl phosphoric acid as a carrier

1997

Abstract Basic studies of a procedure for extraction of amino acids using a supported liquid membrane containing di-2-ethylhexyl phosphoric acid are presented. The extractions are made from an aqueous donor phase with pH 3 to a more acidic acceptor phase and the mass transfer is driven by the proton gradient between these phases. For 0.01 mM tryptophan and with 1 M HCl as acceptor phase, an extraction efficiency of 60% is obtained, constant up to at least 12 h. This permits concentration enrichment factors linearly increasing with time up to values of at least 150. For higher amino acid concentrations, the extraction efficiency is constant only over shorter time intervals.

chemistry.chemical_classificationamino acidsphosphonic acidAqueous solutionChromatographyDEHPAChemistryExtraction (chemistry)TryptophanDi-(2-ethylhexyl)phosphoric acidBiochemistryAcceptorAnalytical ChemistryAmino acidchemistry.chemical_compoundMembranesupported liquid membrane extractiondi-2-ethylhexylEnvironmental ChemistryPhosphoric acidSpectroscopyAnalytica Chimica Acta
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The Effect of Light Intensity During Growth of Sinapis alba on the Electron-Transport and the Noncyclic Photophosphorylation

1975

The photosynthetic rate of Sinapis alba can be modified over a wide range by the light intensity during growth. Our present results indicate that there exist regulatory mechanisms in the field of photosynthetic primary reactions. We compared the effect of different light intensities during growth of Sinapis plants on the concentrations of soluble proteins, manganese and lipophilic plastid quinones, the electron flow from water to ferricyanide and noncyclic phosphorylation. We further determined the light dependence curves for the uncoupled electron transport with ferricyanide as electron acceptor and methylammonium-chloride as an uncoupler of photophosphorylation.

chemistry.chemical_classificationbiologySinapisfood and beverageschemistry.chemical_elementPhotophosphorylationManganeseElectron acceptorPhotochemistryPhotosynthesisbiology.organism_classificationElectron transport chainLight intensitychemistry.chemical_compoundchemistryFerricyanide
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Quinonoid π-extended tetrathiafulvalenes (TTFs)

2001

Publisher Summary Tetrathiafulvalene (TTF) is a fascinating planar πelectron-donor molecule with a broad range of potential applications. TTF and its derivatives play an important role in the field of organic conductors forming charge-transfer (CT) complexes and radical cation salts (Bechgaard salts) with a huge variety of electron-acceptor molecules and anions in the search for electrically conducting and superconducting materials. The chapter focuses on highly π-extended electron donors with p-quinodimethane structures as interesting precursors of materials with non-conventional properties. The first dimeric examples of π-extended TTF derivatives connected through an oxygen atom are also …

chemistry.chemical_classificationchemistry.chemical_compoundCrystallographyFullerenechemistryRadical ionCovalent bondStereochemistryMoietyMoleculeConjugated systemElectron acceptorTetrathiafulvalene
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Über die synthese von oligophenylenes mit einer o-verknüpfung. 10. Mitteilung

1960

Es werden zwei Wege zur Darstellung von Oligophenylenen mit einer o-Winkelung beschrieben. Als Ausgangssubstanzen dienen der Mono-enolather des Cyclohexandion (1,2) bzw. Cyclohexenoxyd. Die Darstellung des Mono-enolathylathers des Cyclohexandion (1,2) wird beschrieben. Durch Oxydation nach OPPENAUER mit Chinon als Wasserstoffacceptor konnen die als Zwischenprodukte der Oligophenylene erhaltenen Cyclohexanolderivate in 90%iger Ausbeute in die benotigten Ketone ubergefuhrt werden. Folgende o-gewinkelten Oligophenylene wurden synthetisiert : o-Terphenyl; 2o2-Quater-phenyl ; 32, 43-Dimethyl-2o2-quaterphenyl ; 3o2-Quinquiphenyl ; 12, 23-Dimethyl-3o2-quinquiphenyl ; 12, 23, 42, 53-Tetramethyl-3o2…

chemistry.chemical_classificationchemistry.chemical_compoundKetonechemistryYield (chemistry)Polymer chemistryMelting pointCyclohexanolOppenauer oxidationAcceptorQuinoneDie Makromolekulare Chemie
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Photoelectrical properties of indandione fragment containing azobenzene compounds

2014

Organic materials are becoming more popular due to their potential application in electronics. Low molecular weight materials possible produce from solution are in special consideration. It gives the possibility to avoid both thermal evaporation in vacuum, and use of polymers in thin film preparation process. Indandione fragment containing azobenzene compounds are one of such materials. These compounds are good candidates for use in design of novel molecular electronic devices due to their possibility to form amorphous structure from solution thus allowing developing flexible, small size systems with low production costs. In this work three indandione fragment containing azobenzene compound…

chemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceAzobenzenechemistryAbsorption spectroscopyOpen-circuit voltageElectron affinityPolymerThin filmPhotochemistryAcceptorAmorphous solidSPIE Proceedings
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NLO Polymers Containing as Active Chromophore in Dandionylpyridinium, Betaine Units: Synthesis, Modeling and Characterization

2000

In present article we report about synthesis, quantum chemical model calculations, non-linear optical characterization and dependencies of the surface potential changes on irradiation with light of novel polyurethane based polymers, namely a bipolar organic compound N-(indan-1,3-dion-2-y1)-4-N’,N’dialkylaminopyridinium betaine (IPB) containing charged electron donor and electron acceptor groups covalently bonded to polyurethane polymer backbone. These newly synthesized IPB containing polymers could be regarded as a promising thermally stable organic non-linear optical materials with long time performance for photonic applications.

chemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceBetainechemistryCovalent bondPolymer chemistryElectron donorPolymerChromophoreElectron acceptorOrganic compoundPolyurethane
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Second-order NLO main-chain polymers by polymerization of poled monomers

1993

A new method of preparing oriented NLO main chain polymers is presented. We synthesized NLO-monomers that consist of donor acceptor substituted tolane molecules that can be poled in the low molar mass state. In the oriented polar state these monomers can be chemically linked using a thermally activated polyaddition reaction. This reaction links the donor head of one monomer to the acceptor tail of the next hibiting bulk noncentrosymmetry with the average direction of the molecular dipoles parallel to the aligning field.

chemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceMolar massMonomerPolymerizationchemistryPolymer chemistryNonlinear opticsMoleculePolymerChromophoreAcceptorNonlinear Optical Properties of Organic Materials VI
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Light-emitting thin films of glassy forming organic compounds containing 2-tert-butyl-6-methyl-4H-pyran-4-ylidene

2012

Low molecular mass organic compounds which make thin films from volatile organic solutions would be great benefit in future organic light emitting systems. Two most important advantages could be mentioned. First - the repetition of synthesis of small molecules is better than for polymers. Second - wet casting methods could be used. In this work we are presenting optical, electroluminescence and amplified spontaneous emission properties of four original glassy forming compounds containing 2-tert-butyl-6-methyl-4H-pyran-4-ylidene fragment as backbone of the molecule. They has the same N,N-dialkylamino electron donating group with incorporated bulky trityloxy ethyl groups. The difference of th…

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryPEDOT:PSSPyranMoleculeElectron acceptorElectroluminescencePhotochemistryOrganic compoundAcceptorMalononitrileOrganic Photonics V
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