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Journal ArticleDOI

Anthryloligothienylporphyrins : energy transfer and light-harvesting systems

TLDR
In this paper, a quantitative intramolecular energy transfer from the anthracene donor to the emitting porphyrin acceptor through the oligothiophene chain after selective UV excitation of Anthracene was demonstrated.
Abstract
In the new trichromophoric supermolecule 1, a quantitative intramolecular energy transfer (>98 %) occurs from the anthracene donor to the emitting porphyrin acceptor through the oligothiophene chain after selective UV excitation of anthracene. Energy-transfer properties and fluorescence quantum yields are independent of the oligothiophene chain length. Attachment of further anthrylquinquethienyl chromophores to the porphyrin ring results in an increase in the intensity of characteristic absorption and fluorescence bands.

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Citations
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Journal ArticleDOI

Functional oligothiophenes: molecular design for multidimensional nanoarchitectures and their applications.

TL;DR: Dithieno[3,2-b:2′3′-d]thiophene-4,4-dioxides 1221 3.3.1.
Journal ArticleDOI

Light Harvesting and Energy Transfer in Laser-Dye-Labeled Poly(aryl ether) Dendrimers

TL;DR: The photophysical properties of a series of laser−dye-labeled poly(aryl ether) dendrimers, generations 1−4, have been determined and these macromolecules have the potential to become integral components of molecular photonic devices.
Journal ArticleDOI

Star-shaped π-conjugated oligomers and their applications in organic electronics and photonics

TL;DR: These structures are monodisperse, well-defined, discrete molecules with 100% synthetic reproducibility, and possess high purity and excellent solubility in common organic solvents and are therefore extremely attractive alternatives to conjugated polymers.
Journal ArticleDOI

Photonic Wires of Nanometric Dimensions. Electronic Energy Transfer in Rigid Rodlike Ru(bpy)32+-(ph)n-Os(bpy)32+ Compounds (ph = 1,4-Phenylene; n = 3, 5, 7)

TL;DR: In this article, the absorption spectrum of each dinuclear complex is essentially equal to the sum of the spectra of the component species, showing that intercomponent electronic interactions are weak.
Patent

Polythiophenes and devices thereof

TL;DR: An electronic device containing a polythiophene wherein R represents a side chain, m represents the number of substituents, A is a divalent linkage, x, y and z represent, respectively, the number Rm substituted thienylenes, unsubstituted thienyenes, and divalent linkages A, respectively in the monomer segment subject to z being 0 or 1, and n represents the repeated monomer segments in the polymer or the degree of polymerization as mentioned in this paper.
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