Search results for "Electron acceptor"

showing 10 items of 83 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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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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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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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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Thermal and optical properties of 4H-pyran-4-ylidene fragment and bis-styryl and triphenyl groups containing derivatives

2014

Small D-π-A type organic molecules with incorporated 4H-pyan-4-ylidene (pyranylidene) fragment in their structures show potential in organic photonics - such as materials for organic light emitting diode application studies and organic solid state lasers. Additional incorporation of bulky triphenyl- groups in their structures gives them the ability to form thin amorphous solid films from volatile non-polar organic solvents. Unfortunately, there is still no clear relation between compound organic structures and their thermal and optical properties. In order to investigate the above mentioned regularities we have synthesized a series of tripheyl- group containing derivates of 2,6-bis-styryl-4…

chemistry.chemical_classificationchemistry.chemical_compoundPhotoluminescenceMaterials sciencechemistryOrganic photonicsThermal decompositionSubstituentElectron acceptorGlass transitionPhotochemistryDichloromethaneAmorphous solidSPIE Proceedings
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Polymere Charge-transfer-Komplexe auf der Basis von Polyvinylalkoholacetalen

1978

Poly[2-(1-naphthyl)-1,3-dioxan-4,6-diylmethylene] (3), poly[2-(2-naphthyl)-1,3-dioxan-4,6-diylmethylene] (5), 1-naphthalenecarbaldehydetrimethyleneacetal (7) and 2-naphthalenecarbaldehydetrimethyleneacetal (8) were synthesized and characterized by UV- and fluorescencespectroscopy. In addition triplet-triplet absorption maxima and triplet-lifetimes were determined by flash technique. The naphthalene derivates were found to act as donors in the charge-transfer complex formation with such electron acceptors as tetracyanoethylene, 2,5-cyclohexadien-1,4-diylidenedimalonodinitrile and 2,4,5,7-tetranitro-9-fluorenone. The equilibrium constants of the charge-transfer complexes were determined spect…

chemistry.chemical_classificationchemistry.chemical_compoundchemistryPolymer chemistryComplex formationAbsorption (chemistry)TetracyanoethyleneElectron acceptorEquilibrium constantNaphthaleneDie Makromolekulare Chemie
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Conjugated Compounds Based on Vinylthiazole Units

2007

Conjugated oligomers attract increasing attention because of their interesting properties in materials science [1]. Moreover, they are model compounds for conjugated polymers. Molecules polarized by electronic effects, in particular push-pull systems having terminal donor-acceptor substitution represent a special class of such oligomers [2]. Their major applications are in the field of nonlinear optics (NLO), twophoton absorption (TPA), two-photon induced fluorescence (TPIF), and photorefractive materials (PR). Fig. 1 illustrates known 2,5-thienylenevinylenes with zwitterionic resonance structures 1 (D = NR2; A = NO2, CHO, SO2R; n = 1, 2) [3, 4]. The corresponding compounds 2 with thiazole …

chemistry.chemical_classificationchemistry.chemical_compoundchemistryThiopheneElectronic effectMoleculeElectron donorGeneral ChemistryConjugated systemElectron acceptorRing (chemistry)ThiazoleMedicinal chemistryZeitschrift für Naturforschung B
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A Tunable, Fullerene‐Based Molecular Amplifier for Vibrational Circular Dichroism

2019

Abstract Vibrational circular dichroism (VCD) studies are reported on a chiral compound in which a fullerene C60 moiety is used as an electron acceptor and local VCD amplifier for an alanine‐based peptide chain. Four redox states are investigated in this study, of which three are reduced species that possess low‐lying electronic states as confirmed by UV/Vis spectroelectrochemistry. VCD measurements in combination with (TD)DFT calculations are used to investigate (i) how the low‐lying electronic states of the reduced species modulate the amplification of VCD signals, (ii) how this amplification depends on the distance between oscillator and amplifier, and (iii) how the spatial extent of the…

endocrine systemFullerenechirality010402 general chemistry01 natural sciencesRedoxCatalysisAnalytical ChemistryElectronic statesMoietychemistry.chemical_classificationFull Paper010405 organic chemistryAmplifierOrganic ChemistryfullerenesspectroelectrochemistryGeneral ChemistryFull PapersElectron acceptorvibrational circular dichroism0104 chemical sciencesCrystallographychemistrydensity functional calculationsVibrational circular dichroismChirality (chemistry)Chemistry – A European Journal
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Chromogenic detection of nerve agent mimics

2008

The current rise in international concern over criminal terrorist attacks via chemical warfare (CW) agents has resulted in an increasing interest in the detection of these lethal chemicals. Among CW species, nerve agents are extremely dangerous and their high toxicity and ease of production underscore the need to detect these deadly chemicals via quick and reliable procedures. A number of detection systems have been developed, most of them based on enzymatic and physical methodologies. However, these usually show limitations such as low selectivity, lack of portability and a certain complexity in their use. An alternative to these classical methods that has been gaining interest in recent y…

musculoskeletal diseasesTertiary amineUNESCO::QUÍMICANerve agent mimicsElectron donorBiosensing TechniquesUNESCO::ASTRONOMÍA Y ASTROFÍSICA:QUÍMICA [UNESCO]Reductive aminationCatalysischemistry.chemical_compoundOrganophosphorus CompoundsMaterials ChemistryMoietyChemical Warfare Agentsskin and connective tissue diseasesChromogenic protocol ; Nerve agent mimics ; Internationalchemistry.chemical_classificationChromogenic protocolMolecular StructureChromogenicChemistryfungiMetals and AlloysGeneral ChemistryElectron acceptorCombinatorial chemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDiethyl chlorophosphatebody regionsKineticsstomatognathic diseasesChromogenic CompoundsInternationalCeramics and CompositesColorimetryHypsochromic shiftAzo Compounds:ASTRONOMÍA Y ASTROFÍSICA [UNESCO]
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