Search results for "Donor acceptor"

showing 10 items of 17 documents

Synthesis of an Acceptor–Donor–Acceptor Multichromophore Consisting of Terrylene and Perylene Diimides for Multistep Energy Transfer Studies

2016

Motivated by the results obtained from the investigation of singlet–singlet annihilation in a linear multichromophore comprising terrylene diimides (TDI) and perylene diimide (PDI) in 2010, we report the detailed process toward the successful synthesis of a TDI–PDI–TDI dyad. Ineffective synthetic pathways, which were necessary for the understanding of the step-by-step construction of the complex multichromophore, are described, leading toward a universal synthetic plan for multicomponent systems containing rylene diimides separated by rigid oligophenylene spacers.

010405 organic chemistryChemistryGeneral Chemical EngineeringEnergy transferGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesAcceptor0104 chemical scienceschemistry.chemical_compoundDiimideMaterials ChemistryMulticomponent systemsDonor acceptorPeryleneChemistry of Materials
researchProduct

Strong donor–acceptor couplings in a special pair-antenna model

2010

A special pair model composed of two cofacial zinc porphyrins (acceptor) linked to a free base (donor) acts as an energy transfer dyad. Despite the absence of conjugation, ππ*/charge transfer excited states and ultrafast energy transfer (∼5 ps) are noted.

ChemistryEnergy transferMetals and Alloyschemistry.chemical_elementFree baseCharge (physics)General ChemistryZincPhotochemistryMolecular physicsAcceptorCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsExcited stateMaterials ChemistryCeramics and CompositesAntenna (radio)Donor acceptorChemical Communications
researchProduct

Large Quadratic Hyperpolarizabilities with Donor–Acceptor Polyenes Exhibiting Optimum Bond Length Alternation: Correlation Between Structure and Hype…

1997

Donor-acceptor polyenes of various lengths, and that combine aro- matic electron-donating moieties with powerful heterocyclic electron-withdraw- ing terminal groups, have been synthe- sized and characterized as efficient non- linear optical (NLO) chromophores. Their linear and nonlinear optical proper- ties have been investigated, and variations in these properties have been related to ground-state polarization (dipole p) and structure. In particular, unprecedented quadratic hyperpolarizabilities (p) have been achieved (up to p(0) =I500 x 10-30esu) by reduction of the bond- length alternation (BLA) in the polyenic chain. In each series of homologous com-

ChemistryOrganic ChemistryBond length alternationAlternation (geometry)Nonlinear opticsHyperpolarizabilityGeneral ChemistryChromophoreCatalysisDipoleCrystallographyQuadratic equationComputational chemistryDonor acceptorChemistry - A European Journal
researchProduct

Oligo(phenylenvinylene) mit terminaler Donor-Acceptor-Substitution

2002

ChemistryStereochemistrySubstitution (logic)General MedicineDonor acceptorAngewandte Chemie
researchProduct

¿Conjugated? Copolymers from a Pechmann Dye Derivative

2016

Conductive polymerMaterials sciencePolymers and PlasticsOrganic Chemistry02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesQuantum chemistry0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical Chemistry0210 nano-technologyDonor acceptorDerivative (chemistry)Macromolecular Chemistry and Physics
researchProduct

ChemInform Abstract: Comparative G2(MP2) Molecular Orbital Study of B3H7XH3 and H3BXH3 Donor-Acceptor Complexes (X: N, P, and As).

2010

B3H7XH3 and H3BXH3 (X = N, P, and As) have been studied as donor−acceptor complex type at the G2(MP2) level of theory. Both single- and double-bridged structures of B3H7 Lewis acid are taken into account. Although the double-bridged structure is energetically favored in the isolated state, the coordination prefers the single-bridged one. The monoborane adducts adopt the staggered arrangement with C3v symmetry. The energetic analysis by natural bond orbital theory shows that the decrease of hyperconjugative contribution upon complexation in the B3H7 moiety has, as consequence, a loss of symmetry for B3H7XH3 (X= P and As) complexes. In the two series, the coordination is the result of two opp…

CrystallographyChemistryMoietyMolecular orbitalGeneral MedicineLewis acids and basesSymmetry (geometry)Donor acceptorAcceptorNatural bond orbitalAdductChemInform
researchProduct

A G2 study of H3BXHn (X=N, O, F, P, S, and Cl) donor–acceptor complexes

1999

Abstract Complexation energies of H3BXHn complexes (X=N, O, F, P, S, and Cl; n=1, 2, 3) have been computed at the G2 level of theory. G2 results show that the H3BXH3 (X=N, P) complexes are more stable than H3BXH2 (X=O, S) and H3BXH (X=F, Cl) ones. This stability was related completely either to the nature of donor compounds, and to the pyramidalization of the monoborane. Two linear correlations were established. The first one is between experimental proton affinity of the XHn donor compounds, and complexation energies of the H3BXHn complexes. The second correlation is between the ∠HBH bond angles and the complexation energies of the H3BXHn complexes calculated at the G2 level of theory.

CrystallographyMolecular geometryComputational chemistryChemistryAb initioProton affinityPhysical and Theoretical ChemistryCondensed Matter PhysicsDonor acceptorBiochemistryJournal of Molecular Structure: THEOCHEM
researchProduct

Synthesis of oxaspiranic compounds through [3 + 2] annulation of cyclopropenones and donor–acceptor cyclopropanes.

2014

The Sc(OTf)3-catalyzed [3 + 2]-annulation reaction between cyclopropenones and donor–acceptor cyclopropanes is described. The process leads directly to the formation of 4-oxaspiro[2.4]hept-1-ene derivatives in good to excellent reaction yields. Density functional theory calculations suggest that the [3 + 2]-annulation pathway is strongly preferred over the possible [3 + 3]-process.

CyclopropanesMesylatesAnnulationMolecular StructureChemistryOrganic ChemistryStereoisomerismCatalysisComputational chemistryDensity functional theorySpiro CompoundsCycloheptanesDonor acceptorScandiumThe Journal of organic chemistry
researchProduct

Comparative G2(MP2) molecular orbital study of [H 3 AlX(CH 3 ) 2 ] − (X=N, P, and As) and H 3 AlY(CH 3 ) 2 (Y=O, S, and Se) donor–acceptor complexes

2001

Abstract [H3AlX(CH3)2]− (X=N, P, and As) and H3AlY(CH3)2 (Y=O, S, and Se) donor–acceptor complexes have been studied using G2(MP2) level of theory. The coordination mode, the structural and the methyl substitution effects upon complexation are analyzed. The interaction of the alane with the donor ligand is stronger in the anionic complexes than in the neutral ones and the methylated complexes are more stable than the hydrogenated ones. The coordination is ensured by tow interactions having a reverse character: interaction between a′ symmetry fragment molecular orbital (stabilizing) and interaction between a″ symmetry occupied molecular orbital (destabilizing) of the two fragments. A linear …

LigandStereochemistryChemistryMolecular orbitalCharge (physics)Physical and Theoretical ChemistryLinear correlationCondensed Matter PhysicsDonor acceptorBiochemistryFragment molecular orbitalNatural bond orbitalJournal of Molecular Structure: THEOCHEM
researchProduct

Oligo(phenylenevinylene)s with Terminal Donor–Acceptor Substitution This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der …

2002

Materials scienceTerminal (electronics)StereochemistrySubstitution (logic)General ChemistryDonor acceptorCatalysisAngewandte Chemie International Edition
researchProduct