Search results for "Acceptor"

showing 10 items of 394 documents

Spin‐Crossover 2D Metal–Organic Frameworks with a Redox‐Active Ligand: [Fe(ttf‐adpy) 2 M(CN) 4 ]· n H 2 O (ttf‐adpy = 4‐Tetrathiafulvalenylcarboxamid…

2008

A new ttf (tetrathiofulvalene) ligand containing an amidopyridine moiety was synthesized and characterized. The electrochemical study of the 4-tetrathiofulvalenylcarboxamidopyridine (ttf–adpy) ligand showed two reversible oxidation processes at EI′1/2 = 0.08 V/Fc+–Fc and EII′1/2 = 0.26 V/Fc+–Fc. The crystal structure of [(ttf–adpyH)2Pt(CN)4] (1) was solved at 293 K, where 1 displays the triclinic space group P. The ttf–adpyH+ molecule is planar, and the bond lengths within the ttf core are in the usual range for neutral ttf moieties. The ttf–adpyH+ molecules and the [Pt(CN)4]2– anions organize in a three-dimensional network by means of hydrogen bonds and short S···S contacts. In the network…

Inorganic ChemistryCrystallographyChemistryHydrogen bondLigandSpin crossoverInorganic chemistrySpin transitionMoleculeMetal-organic frameworkCrystal structureAcceptorEuropean Journal of Inorganic Chemistry
researchProduct

A Trinuclear Aqua Cyano‐Bridged Ruthenium Complex [{(η 5 ‐C 5 H 5 )(PPh 3 ) 2 Ru(μ‐CN)} 2 RuCl 2 (PPh 3 )(H 2 O)]PF 6 : Synthesis, Characterization a…

2007

The organometallic trinuclear aqua cyano-bridged complex [{(η5-C5H5)(PPh3)2Ru(μ-CN)}2RuCl2(PPh3)(H2O)]PF6 (1), in which the fragment [RuCl2(PPh3)(H2O)] acts as a bridge and an acceptor group between the two terminal cyclopentadienyl ruthenium cyano moieties, was isolated in moderate yield from the reaction of [(η5-C5H5)(PPh3)2RuCN] with [RuCl2(PPh3)3] in THF. To the best of our knowledge, compound 1 is one of the few examples of a trinuclear array of ruthenium fragments bridged by the nitrogen atom of the–C≡N– group (Ru–C≡N–Ru′–N≡C–Ru) with a Ru-coordinated water molecule. The new aqua complex was structurally characterized by FTIR, 1H, 13C, and 31P NMR spectroscopy, mass spectrometry, elem…

Inorganic ChemistryCrystallographyCyclopentadienyl complexchemistryStereochemistryYield (chemistry)Moleculechemistry.chemical_elementCrystal structureTriclinic crystal systemCyclic voltammetryAcceptorRutheniumEuropean Journal of Inorganic Chemistry
researchProduct

1,2,3,4,5‐[1′,8′] Anthra‐8,9;10,11‐dibenzo[13]annulene and 1,8‐Distyrylanthracene as Models for Phenylenevinylene Species. Syntheses, Structures, and…

1987

The synthesis of the title compound 4, formally a [13] perimeter, and of its acyclic model system, 1,8-distyrylanthracene (6) is described. The crystal structure of 4 reveals the configuration of the double bonds and the conformation of the macrocycle. Related findings come from the 1H-NMR spectroscopic characterization of 4 and 6 in solution. The spin density distribution of the radical anions 4−· and 6−· is interpretet in terms of the singly occupied molecular orbital and of the prevailing geometry. In contrast to 4, compund 6 proves to be an efficient electron acceptor since it can even be reduced to a tetraanion salt. The complete redox sequence is characterized by NMR and ESR spectrosc…

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundDouble bondStereochemistryChemistryMoleculeMolecular orbitalNuclear magnetic resonance spectroscopyCrystal structureAnnuleneElectron acceptorCyclophaneChemische Berichte
researchProduct

Tuning Reductive and Oxidative Photoinduced Electron Transfer in Amide‐Linked Anthraquinone–Porphyrin–Ferrocene Architectures

2014

Porphyrin amino acids 3a–3h with meso substituents Ar of tunable electron-donating power (Ar = 4-C6H4OnBu, 4-C6H4OMe, 4-C6H4Me, Mes, C6H5, 4-C6H4F, 4-C6H4CF3, C6F5) have been linked at the N terminus to anthraquinone Q as electron acceptor through amide bonds to give Q-PAr dyads 4a–4h. These were conjugated to ferrocene Fc at the C terminus as electron donor to give the acceptor-chromophore-donor Q-PAr-Fc triads 6a–6h. To further modify the energies of the electronically excited and charge-separated states, the triads 6a–6h were metallated with zinc(II) to give the corresponding Q-(Zn)PAr-Fc triads Zn-6a–Zn-6h. The Q-PAr1 dyad (Ar1 = C6H5) was further extended with a second porphyrin PAr2 (…

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundElectron transferFerrocenechemistryElectron donorElectron acceptorChromophorePhotochemistryPorphyrinPhotoinduced electron transferQuinoneEuropean Journal of Inorganic Chemistry
researchProduct

Carbazole-based green and blue-BODIPY dyads and triads as donors for bulk heterojunction organic solar cells.

2020

Two BODIPY derivatives with one (B2) and two (B3) carbazole moieties were synthesized and applied as electron-donor materials in organic photovoltaic cells (OPV). Their optical and electrochemical properties were systematically investigated. These BODIPY dyes exhibit excellent solubility in organic solvents and present high molar extinction coefficients (1.37–1.48 × 105 M−1 cm−1) in solutions with absorption maxima at 586 nm for mono-styryl groups and at 672 nm for di-styryl groups. The introduction of the styryl moieties results in a large bathochromic shift and a significant decrease in the HOMO–LUMO energy-gaps. The BODIPY dyes show relatively low HOMO energies ranging from −4.99 to −5.1…

Inorganic Chemistrychemistry.chemical_compoundMaterials sciencechemistryOrganic solar cellCarbazoleBathochromic shiftMolecular orbitalCyclic voltammetryBODIPYPhotochemistryAcceptorPolymer solar cellDalton transactions (Cambridge, England : 2003)
researchProduct

Au70S20(PPh3)12: an intermediate sized metalloid gold cluster stabilized by the Au4S4 ring motif and Au-PPh3 groups

2018

Reducing (Ph3P)AuSC(SiMe3)3 with L-Selectride® gives the medium-sized metalloid gold cluster Au70S20(PPh3)12. Computational studies show that the phosphine bound Au-atoms not only stabilize the electronic structure of Au70S20(PPh3)12, but also behave as electron acceptors leading to auride-like gold atoms on the exterior.

Inorganic chemistry02 engineering and technologyElectronic structure010402 general chemistryRing (chemistry)01 natural scienceskultaCatalysischemistry.chemical_compoundMaterials Chemistryta116chemistry.chemical_classificationGold clusterChemistryMetals and AlloysGeneral ChemistrygoldElectron acceptor021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyCeramics and CompositesnanohiukkasetnanoparticlesMetalloid0210 nano-technologyPhosphineChemical Communications
researchProduct

Light-induced charge separation in a donor–chromophore–acceptor nanocomposite poly[TPA-Ru(tpy)2]@ZnO

2013

The synthesis and characterisation of a new donor–chromophore–acceptor system based on poly(vinyltriphenylamine) as the electron donor and a glycine-functionalised bis(2,2′;6′,2′′-terpyridine)ruthenium(II) complex acting both as a chromophore and as an anchor group attached to ZnO nanorods as the electron acceptor are described. The TPA-containing block copolymer was synthesised by Reversible Addition Fragmentation Chain Transfer (RAFT) polymerisation and the ruthenium complex glycine conjugates prepared by Solid Phase Peptide Synthesis (SPPS) were attached via post-polymerisation esterification. GPC, NMR, IR and UV-Visible spectroscopy were used to characterise the multifunctional chromoph…

Kelvin probe force microscopechemistry.chemical_classificationQuenching (fluorescence)Materials sciencechemistry.chemical_elementElectron donorGeneral ChemistryChromophoreElectron acceptorPhotochemistryAcceptorRutheniumchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryJ. Mater. Chem. C
researchProduct

Studies on proton acceptor ability of SOx-containing compounds

1995

Abstract IR spectra, dipole moments and molar Kerr constants of complexes of phenols with compounds containing SO x groups were studied to establish the structure of the complexes and the parameters characterizing the proton acceptor capability of these compounds. ( μ H , Δ ( mK ), log K and δ 0 ). It has been suggested that the new parameter Δ ( mK ) — the structural additive difference of the molar Kerr constant — makes it possible to determine changes of polarity and polarizability of the systems during complex formation.

Kerr constantPolarity (physics)Organic ChemistryComplex formationAnalytical chemistryInfrared spectroscopyAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundDipolechemistryPolarizabilityPhysical chemistryPhenolsProton acceptorSpectroscopyJournal of Molecular Structure
researchProduct

Studies on the proton acceptor ability of phosphoryl compounds

1996

Abstract Dipole moments and molar Kerr constants of complexes of phenols with phosphoryl compounds were studied to establish the structure of complexes and parameters characterizing the proton acceptor ability of these compounds. The structures of these complexes and parameters ( μ H , Δ ( mk ) S , log K and δ 0 ) were established. It has been suggested that a new parameter Δ ( mK ) S — structural additive difference of the molar Kerr constant — makes it possible to determine changes of polarity and polarizability of the systems during complex formation.

Kerr constantStereochemistryPolarity (physics)Organic ChemistryComplex formationAnalytical ChemistryInorganic ChemistryDipolechemistry.chemical_compoundCrystallographychemistryPolarizabilityPhenolsProton acceptorSpectroscopyJournal of Molecular Structure
researchProduct

Stereodifferentiation in the formation and decay of the encounter complex in bimolecular electron transfer with photoactivated acceptors.

2005

Experimental evidence has been obtained for the involvement of encounter complexes between both enantiomers of a π,π* triplet excited ketone and a chiral phenol or indole. Determination of the pre-equilibrium constants (KEC) and the intrinsic decay rate constants (kd) indicates a significant stereodifferentiation in both steps of the quenching process. Perez Prieto, Julia, Julia.Perez@uv.es ; Galian, Raquel Eugenia, Raquel.Galian@uv.es ; Morant Miñana, Maria Carmen, Maica.Morant@uv.es

KetoneFormation and decayUNESCO::QUÍMICAPhotochemistry:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundElectron transferBimolecular electronReaction rate constantMaterials ChemistryPhenolUNESCO::QUÍMICA::Química orgánicaStereodifferentiatioPhotoactivated acceptorschemistry.chemical_classificationIndole testQuenching (fluorescence):QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryExcited statePhotoactivated acceptors ; Bimolecular electron ; Stereodifferentiatio ; Formation and decayCeramics and CompositesEnantiomerChemical communications (Cambridge, England)
researchProduct