Search results for "CHROMOPHORE"

showing 10 items of 309 documents

Dendrimers with peripheral stilbene chromophores

2006

Abstract Two types of dendritic nanoparticles were prepared, which contain ( E )-stilbene chromophores in the terminal positions of the dendrons. The compounds showed a highly efficient photoreactivity in the course of which statistical CC bond formations led to a crosslinking of the particles. Finally, all stilbene chromophores reacted and the typical ( E )-stilbene absorption and fluorescence disappeared completely.

ChemistryDendrimerOrganic ChemistryDrug DiscoveryNanoparticleChromophoreAbsorption (chemistry)PhotochemistryBiochemistryFluorescenceTetrahedron
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Poly(propylene imine) dendrimers functionalized with stilbene or 1,4-distyrylbenzene chromophores

2007

Abstract Two generations of dendritic nanoparticles were prepared, which contain ( E )-stilbene or ( E , E )-1,4-distyrylbenzene chromophores in the 4 or 8 terminal positions of the propylene imine dendrons. The compounds show a highly efficient photoreactivity. On prolonged irradiation all stilbenoid chromophores were destroyed by oligomerization (crosslinking) and the typical absorption and fluorescence of the chromophores disappeared completely.

ChemistryDendrimerOrganic ChemistryDrug DiscoveryPolymer chemistryNanoparticleChromophorePropylene imineStilbenoidAbsorption (chemistry)PhotochemistryBiochemistryFluorescenceTetrahedron
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ChemInform Abstract: Poly(propylene imine) Dendrimers Functionalized with Stilbene or 1,4-Distyrylbenzene Chromophores.

2008

Abstract Two generations of dendritic nanoparticles were prepared, which contain ( E )-stilbene or ( E , E )-1,4-distyrylbenzene chromophores in the 4 or 8 terminal positions of the propylene imine dendrons. The compounds show a highly efficient photoreactivity. On prolonged irradiation all stilbenoid chromophores were destroyed by oligomerization (crosslinking) and the typical absorption and fluorescence of the chromophores disappeared completely.

ChemistryDendrimerPolymer chemistryNanoparticleGeneral MedicineAbsorption (chemistry)ChromophorePropylene imineStilbenoidFluorescenceChemInform
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Crystal and molecular structure and electronic properties of [Cu(phen)2(HL)] · (phen)0.5 · 7H2O (H3L = 1,3,5-triazine-2,4,6(1H,3H,5H)-trione), a nove…

1998

Abstract The crystal and molecular structure of [Cu(phen)2(HL) · (phen)0.5 · 7H2O (H2L = 1,3,5-triazine-2,4,6(1H,3H,5H)-trione) has been determined by X-ray diffraction methods. The structure is built up of neutral [Cu(phen)2(HL)] entities (which are associated to form dinuclear units through hydrogen bonds involving the cyanurate ions), uncoordinated phenanthroline and crystallisation water molecules. The copper atom is involved in a CuN5 chromophore, with an stereochemistry near to a compressed trigonal bipyramid (TBP) but with a significant degree of distortion towards the square pyramidal (SP) topology. The EPR spectrum is indicative of a mixed d z 2 d x 2 −y 2 ground state for the copp…

ChemistryHydrogen bondPhenanthrolineCrystal structureChromophoreSquare pyramidal molecular geometrylaw.inventionInorganic ChemistryCrystallographyTrigonal bipyramidal molecular geometrychemistry.chemical_compoundlawMaterials ChemistryMoleculePhysical and Theoretical ChemistryElectron paramagnetic resonancePolyhedron
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Coordination behavior of sulfathiazole. Crystal structure of [Cu (sulfathiazole) (py)3Cl] superoxide dismutase activity

1995

Abstract The preparation, spectroscopic, magnetic properties, and crystal structure of [Cu(stzxpy) 3 Cl] (stz − stands for the deprotonated form of sulfathiazole, 4-amino-N-2-thiazolylbencenosulfonamide) are reported. Crystals are orthorhombic, space group Pbca, with cell constants a = 15.834(2), b = 17.512(4), and c = 18.79(2) A, and Z = 8. The structure was solved and refined to R = 0.041 (R W = 0.040). The structure consists of mononuclear units linked via hydrogen bonds to form the tridimensional pyramid. The geometry of CuN3N*NCl chromophore is distorted square-pyramid. The superoxide-dismutase mimetic activity of the compound is measured and compared with those of the SOD enzyme, the …

ChemistryHydrogen bondSuperoxide dismutase activityCrystal structureChromophoreBiochemistryInorganic ChemistryCrystallographySulfathiazoleDeprotonationmedicineOrthorhombic crystal systemFree drugmedicine.drugJournal of Inorganic Biochemistry
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Comparison of Alkoxy-substituted 4,4´-Distyrylbiphenyls and the Corresponding 4,4´-Distyrylbenzenes

2008

Abstract Configurationally highly pure (E,E)-4,4´-bis(styryl)biphenyls 2a - e were obtained by Siegrist reactions of 4,4´-dimethylbiphenyl 3 and alkoxy-substituted benzaldimines (4a - e). DSC measurements have indicated different crystalline modifications of these conjugated compounds. The stilbenoid chromophores of 2a - e are compared to the stilbenoid chromophores in the OPV series, which have a similar length of conjugation. The intense fluorescence and the high transparency in the visible region are promising properties for an application of the donor-substituted compounds 2a - e in twophoton absorption (TPA) techniques.

ChemistryIntense fluorescenceAlkoxy groupGeneral ChemistryAbsorption (chemistry)StilbenoidConjugated systemChromophoreCondensation reactionPhotochemistryFluorescenceZeitschrift für Naturforschung B
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Soluble oligo(phenylenevinylene)s with electron withdrawing substituents for the use in light emitting diodes

2000

Poly(p-phenylenevinylene) (PPV) and its derivatives are one of the most widely used classes of phosphors in light emitting diodes. Central problems are the imbalanced charge carrier injection and transport properties due to the high lying conduction band. A series of good soluble oligo(phenylenevinylene)s (OPV) with five benzene rings and a variety of electron withdrawing and accepting substituents have been prepared and may serve as model compounds for PPV with increased electron affinity. The central ring of the OPVs is substituted with two octyloxy groups to ensure good solubility and the lateral styrene units carry further chromophoric groups of different electronic character. The synth…

ChemistryMechanical EngineeringAuxochromeMetals and AlloysChromophoreCondensed Matter PhysicsCondensation reactionPhotochemistryFluorescenceElectronic Optical and Magnetic MaterialsUltraviolet visible spectroscopyMechanics of MaterialsElectron affinityMaterials ChemistryPolar effectKnoevenagel condensationSynthetic Metals
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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
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Extension of Conjugation Leading to Bathochromic or Hypsochromic Effects in OPV Series

2004

Four OPV series 1-4 (a-d) with a terminal dialkylamino group as electron donor were prepared by Wittig-Horner reactions. To study the influence of the push-pull effect on the long-wavelength absorption, three of the four series contained terminal acceptor groups (CN, CHO, NO(2)). The length of the chromophores strongly affects the intramolecular charge transfer (ICT)-an effect which superimposes upon the extension of the conjugation. Increasing numbers n of repeat units cause an overall bathochromic shift for the purely donor-substituted series 1 a-4 a and the series 1 b-4 b with CN as weak acceptor. The two effects annihilate each other in the series 1 c-4 c with terminal CHO groups, so th…

ChemistryOrganic ChemistryElectron donorProtonationGeneral ChemistryChromophorePhotochemistryAcceptorCatalysischemistry.chemical_compoundAtomic electron transitionIntramolecular forceBathochromic shiftHypsochromic shiftChemistry - A European Journal
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Probing the spectral dynamics of single terrylenediimide molecules in low-temperature solids

1999

Abstract Fluorescence excitation lines of single terrylenediimide (TDI) molecules were recorded in the matrices polyethylene (PE) and hexadecane (HD) in the temperature range between 1.4 and 13 K. From line width distributions at 2.5 K in both matrices it was concluded that the disorder, theoretically modeled by a distribution of two-level systems (TLSs), is about three times stronger in PE. Temperature-dependent measurements of the line shape of single chromophores showed a reversible broadening and shift of the zero-phonon lines. We attributed this behavior to dephasing caused by pseudolocal phonons and to spectral diffusion caused by fluctuating TLSs of the disordered host. Following the…

ChemistryPhononDephasingAnalytical chemistryGeneral Physics and AstronomyChromophoreHexadecaneAtmospheric temperature rangeMolecular physicschemistry.chemical_compoundPhysical and Theoretical ChemistryDiffusion (business)ExcitationLine (formation)Chemical Physics
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