Search results for "J-aggregate"

showing 4 items of 4 documents

Quantum Chemical Parametrization and Spectroscopic Characterization of the Frenkel Exciton Hamiltonian for a J-Aggregate Forming Perylene Bisimide Dye

2012

Quantum chemical and quantum dynamical calculations are performed for a bay-substituted perylene bisimide dye up to its hexameric aggregate. The aggregate structure is determined by employing the self-consistent charge density functional tight-binding (SCC-DFTB) approach including dispersion corrections. It is characterized by a stabilization via two chains of hydrogen bonds facilitated by amide functionalities. Focusing on the central embedded dimer, the Coulomb coupling for this J-aggregate is determined by means of the time-dependent density functional theory (TDDFT) to be -514 cm(-1). Exciton vibrational coupling is treated within the shifted oscillator model from which five strongly co…

Molecular StructureAbsorption spectroscopyChemistryExcitonCharge densityTime-dependent density functional theoryImideschemistry.chemical_compoundQuantum TheoryDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsRotational–vibrational couplingPeryleneJ-aggregatePeryleneFluorescent DyesThe Journal of Physical Chemistry A
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J-aggregates prepared by adsorption at monolayer/water interfaces

1991

By adsorption of anionic cyanine dyes at positivly charged lipid monolayers large J-aggregates are formed. Absorption and fluorescence spectra are measured at the air/water interface during the crystallization process. The influence of the lipid/dye interaction on the aggregate structure is studied for two different systems. It is shown that the aggregate structure can be improved by growing crystals from a seed.

Polymers and PlasticsChemistryOrganic ChemistryInorganic chemistryCrystal growthCondensed Matter Physicslaw.inventionchemistry.chemical_compoundAdsorptionChemical engineeringlawAggregate structureMonolayerMaterials ChemistryCrystallizationCyanineAbsorption (chemistry)J-aggregateMakromolekulare Chemie. Macromolecular Symposia
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N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates

2020

The unique self-assembling features of N-annulated perylene bisimides (PBIs) 1 and 2 are reported. The stability of the aggregates of diester 1, in which no H-bonding interactions are operative, corroborates the significance of long-range van der Waals and dipole-dipole electrostatic interactions in the construction of stable supramolecular assemblies. The incorporation of amide functional groups within the N-annulated PBI in 2 stimulates pathway differentiation to achieve up to three J-type aggregates and a fourth H-type aggregate depending on the experimental conditions. The results presented demonstrate unprecedented levels of control over synthetic supramolecular self-assembly and the r…

chemistry.chemical_classification010405 organic chemistryChemistrySupramolecular chemistryGeneral ChemistryPolymerGeneral Medicine010402 general chemistryElectrostatics01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographysymbols.namesakeMetastabilityAmidesymbolsvan der Waals forceJ-aggregatePeryleneAngewandte Chemie
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Inside Back Cover: N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates (Ange…

2020

chemistry.chemical_compoundCrystallographyMaterials sciencechemistryMetastabilitySupramolecular chemistryCover (algebra)General ChemistryJ-aggregateCatalysisPeryleneAngewandte Chemie International Edition
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