The regioselective synthesis of three sexithiophenes characterised by the presence of one central 3,3'-dimethyl-2,2'-bithiophene subsystem is described.One of these compounds was obtained under mild conditions by microwave-mediated synthesis. All sexithiophenes were soluble in organic solvents and displayed 30-40% fluorescence quantum yield in solution. In thin films the fluorescence quantum yield dropped to 1-2% indicating conformational changes and strong intermolcular interactions in the solid state.

Synthesis and optical properties of soluble sexithiophenes with one central head-to-head junction

Sotgiu G;Zambianchi M;Barbarella G;Botta C
2002

Abstract

The regioselective synthesis of three sexithiophenes characterised by the presence of one central 3,3'-dimethyl-2,2'-bithiophene subsystem is described.One of these compounds was obtained under mild conditions by microwave-mediated synthesis. All sexithiophenes were soluble in organic solvents and displayed 30-40% fluorescence quantum yield in solution. In thin films the fluorescence quantum yield dropped to 1-2% indicating conformational changes and strong intermolcular interactions in the solid state.
2002
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
Istituto per lo Studio delle Macromolecole - ISMAC - Sede Milano
CROSS-COUPLING REACTIONS
ORGANIC ELECTROPHILES
THIOPHENE OLIGOMERS
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/166563
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