Search results for "Acceptor"

showing 10 items of 394 documents

Photoinduced electron transfer in molecular organizates at the gas-water interface

1994

Abstract The influence of the molecular geometry is of fundamental importance for a better understanding of the photoinduced electron transfer mechanism. Because of their typical molecular structures, cyclophane rings have proved to be suitable for this purpose as electron acceptor molecules adsorbed under an amphiphile monolayer. We used a pyrene-labelled phospholipid derivative both as molecular anchor for the cyclophane ring and electron donor molecule. The co-spreading technique was used to prepare the complex monolayers. Surface pressure and surface potential measurements have indicated similar monolayer behaviour as with dimyristoylphosphatidic acid as anchor molecule, leading to the …

chemistry.chemical_classificationQuenching (fluorescence)ChemistryMetals and AlloysElectron donorSurfaces and InterfacesElectron acceptorPhotochemistryPhotoinduced electron transferSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferMonolayerMaterials ChemistryPyreneCyclophaneThin Solid Films
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The Aerobic and Anaerobic Respiratory Chain of Escherichia coli and Salmonella enterica: Enzymes and Energetics.

2014

Escherichia coli contains a versatile respiratory chain that oxidizes 10 different electron donor substrates and transfers the electrons to terminal reductases or oxidases for the reduction of six different electron acceptors. Salmonella is able to use two more electron acceptors. The variation is further increased by the presence of isoenzymes for some substrates. A large number of respiratory pathways can be established by combining different electron donors and acceptors. The respiratory dehydrogenases use quinones as the electron acceptors that are oxidized by the terminal reductase and oxidases. The enzymes vary largely with respect to their composition, architecture, membrane topolog…

chemistry.chemical_classificationRespiratory chainElectron donorBiologyElectron acceptormedicine.disease_causeMicrobiologyElectron transport chainRedoxIsozymechemistry.chemical_compoundEnzymeBiochemistrychemistrymedicineEscherichia coliEcoSal Plus
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A Comparison of Shuttling Mechanisms in Two Constitutionally Isomeric Bistable Rotaxane-Based Sunlight-Powered Nanomotors

2006

To find out how best to optimize shuttling of the macrocycle in a particular class of photochemically driven molecular abacus, which has the molecular structure of BR-I6+ in its Mark I prototype (Ashton et al., Chem. Eur. J. 2000, 6, 3558), we have synthesized and characterized a Mark II version of this kind of two-station rotaxane comprised of six molecular modules, namely (a) a bisparaphenylene[34]crown-10 electron donor macrocycle M and its dumbbell-shaped component which contains (b) a Ru(ii)-polypyridine photoactive unit P2+ as one of its stoppers, (c) a p-terphenyl-type ring system as a rigid spacer S, (d) 4,4′-bipyridinium (A12+) and (e) 3,3′-dimethyl-4,4′-bipyridinium (A22+) electr…

chemistry.chemical_classificationRotaxaneChemistryStereochemistrySupramolecular chemistryElectron donorGeneral ChemistryCrystal structureElectron acceptorRing (chemistry)CrystallographyElectron transferchemistry.chemical_compoundDensity functional theoryAustralian Journal of Chemistry
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ChemInform Abstract: Epoxidation of Olefins with a Silica-Supported Peracid.

2012

Anhydrous [2-percarboxyethyl] functionalized silica (2a) is an advantageous oxidant for performing the epoxidation of olefins 1. Epoxides 3 do not undergo the ring-opening reactions catalyzed by the acidic silica surface, except for particularly activated cases such as styrene oxide. The hydrophilic and acidic character of the silica surface does not interfere with the directing effects exerted by allylic H-bond acceptor substituents. The alkenes 1 carrying hydroxyl groups react with silica-supported peracid 2a faster than unsubstituted alkenes, thus reversing the trend known for reactions with soluble peracids. These results are attributed to the H-bond interactions of substrate 1 with the…

chemistry.chemical_classificationSilanolchemistry.chemical_compoundAllylic rearrangementchemistryCarboxylic acidStyrene oxidePolymer chemistryAnhydrousSubstrate (chemistry)General MedicineAcceptorCatalysisChemInform
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Studien zum Vorgang der Wasserstoffübertragung, 53. Beitrag zur Kenntnis der elektroreduktiven Spaltung von Hydroxylaminderivaten

1978

Die Elektroreduktion von 26 Hydroxylaminderivaten wird polarographisch und an 6 Beispielen praparativ untersucht. Es wurde gefunden: 1) Dreifach mit Alkyl- oder Arylgruppen substituierte Hydroxylaminderivate werden bis zu einem Potential von -2.5 V (gegen Ag/AgCl/KClges.) nicht elektroreduziert. — 2) Der Einbau von Acylgruppen erleichtert in Abhangigkeit von Art, Zahl und Verknupfungsstelle die Elektroreduktion. Acylreste mit aromatischen Gruppen verschieben das Halbstufenpotential starker nach positiven Werten als aliphatisch substituierte Acylreste (entsprechend: Phthaloyl > Benzoyl > Formyl > Acetyl > Ethoxycarbonyl). Acylgruppen am Sauerstoff des Hydroxylamins fordern die Elektroredukti…

chemistry.chemical_classificationStereochemistryArylOrganic ChemistryHydrogen transferElectron acceptorRing (chemistry)chemistry.chemical_compoundHydroxylaminechemistryHydroxylamine derivativesPhysical and Theoretical ChemistryMethyleneAlkylJustus Liebigs Annalen der Chemie
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Push-Pull Oligomers with 2,2-Dicyanovinyl Groups as Electron Acceptors

2007

Three conjugated oligomer series with terminal donor–acceptor substitution were studied: oligo(1,4-phenylenevinylene)s DAOPVs 4a–d (n = 1–4), oligo(1,4-phenyleneethynylene)s DAOPEs 6a–d (n = 1–4) and oligo(2,5-thienyleneethynylene)s DAOTEs 8a–e (n = 1–5). Dialkylamino or methoxy groups served as electron donors and 2,2-dicyanovinyl groups as strong electron acceptors. The push-pull effect polarizes the molecular chains – an effect which is documented by the splitting of the 13C chemical shifts of two carbon atoms of the double or triple bonds in the chain. For higher oligomers (n ≥ 3), the effect is mainly localized at the chain ends. The long-wavelength absorption results in a charge-trans…

chemistry.chemical_classificationStereochemistryChemical shiftOrganic ChemistryChromophoreConjugated systemElectron acceptorTriple bondOligomerchemistry.chemical_compoundCrystallographychemistryIntramolecular forceHypsochromic shiftPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Star-Shaped Compounds Having 1,3,5-Triazine Cores

2003

The 1,3,5-triazine derivatives 1−4 having styryl or higher oligo(phenylenevinylene) chains in the 2-, 4-, and 6-positions represent star-shaped push-pull compounds. Alkoxy or dimethylamino groups on the peripheral benzene rings, which act as electron donors, and the central 1,3,5-triazine ring, which acts as an electron acceptor, cause intramolecular charge transfer (ICT) to occur in the absorption S0⇄S1. Protonation of the 1,3,5-triazine core enhances the effect, as demonstrated by a bathochromic shift; a secondary protonation on the dimethylamino groups, however, leads to the breakdown of the ICT. Thus, the yellow compound 1d first becomes violet and then colorless upon the addition of tr…

chemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryProtonationElectron acceptorMedicinal chemistrychemistry.chemical_compound135-TriazineIntramolecular forceBathochromic shiftAlkoxy groupTrifluoroacetic acidPhysical and Theoretical ChemistryAbsorption (chemistry)European Journal of Organic Chemistry
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ChemInform Abstract: Conjugated Compounds Based on Vinylthiazole Units.

2008

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_classificationStereochemistryElectron donorGeneral MedicineConjugated systemElectron acceptorRing (chemistry)Medicinal chemistrychemistry.chemical_compoundchemistryThiopheneElectronic effectMoleculeThiazoleChemInform
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Star-Shaped Push-Pull Compounds Having 1,3,5-Triazine Cores

2006

The 1,3,5-triazines 9–11 having OPV chains in the 2-, 4- and 6-position represent star-shaped compounds which exhibit strong push-pull effects. Their long-wavelength absorption S0 S1 is characterized by an intramolecular charge transfer (ICT) from the dialkylamino group as electron donor D via the conjugated chain to the 1,3,5-triazine core as electron acceptor A. Protonation of the dialkylamino group removes the donor capability, whereas protonation of the 1,3,5-triazine ring enhances the acceptor strength. Thus, the prevailing protonation site has a crucial influence on the push-pull effect and the ICT. The transition energies ΔE (S0 S1) pass through a minimum for the second generation 10…

chemistry.chemical_classificationStereochemistryOrganic ChemistryElectron donorProtonationElectron acceptorConjugated systemRing (chemistry)Acceptorchemistry.chemical_compoundCrystallographychemistry135-TriazineIntramolecular forcePhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Conjugated Oligomers with Terminal Donor–Acceptor Substitution

2005

Conjugated oligomers represent a prominent class of compounds from a viewpoint of their theory, synthesis, and applications in materials science. Push-pull substitution with an electron donor D at one end of the conjugation and an electron acceptor A at the other end results in them having outstanding optical and electronical properties. This Review highlights fundamental synthetic strategies for the preparation of such oligomers with n repeat units (n=1, 2, 3, 4, ..) and the rules that govern their linear and nonlinear optical properties (absorption, frequency doubling and tripling). The unification of chemical, physical, and theoretical aspects with an interdisciplinary image of this clas…

chemistry.chemical_classificationStereochemistrySubstitution (logic)Nonlinear opticsElectron donorGeneral MedicineGeneral ChemistryConjugated systemElectron acceptorCombinatorial chemistryCatalysisNonlinear opticalchemistry.chemical_compoundchemistryTerminal (electronics)Absorption (chemistry)Donor acceptorAngewandte Chemie International Edition
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