Stable, crystalline acenedithiophenes with up to seven linearly fused rings

Marcia M. Payne; Susan A. Odom; Sean R. Parkin; John E. Anthony

doi:10.1021/ol048686d

Stable, crystalline acenedithiophenes with up to seven linearly fused rings

Marcia M. Payne, Susan A. Odom, Sean R. Parkin, John E. Anthony

Chemistry

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218 Scopus citations

Abstract

(Chemical Equation Presented) We report the synthesis of a series of crystalline acenedithiophenes with up to seven linearly fused rings and silylethynyl substituents. These functional groups are designed to both improve solubility and enhance cofacial interactions in the solid. We discuss the crystal packing of these materials, as well as their physical properties such as oxidation potential, UV-vis absorption, fluorescence emission, and decomposition pathways.

Original language	English
Pages (from-to)	3325-3328
Number of pages	4
Journal	Organic Letters
Volume	6
Issue number	19
DOIs	https://doi.org/10.1021/ol048686d
State	Published - Sep 16 2004

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol048686d

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title = "Stable, crystalline acenedithiophenes with up to seven linearly fused rings",

abstract = "(Chemical Equation Presented) We report the synthesis of a series of crystalline acenedithiophenes with up to seven linearly fused rings and silylethynyl substituents. These functional groups are designed to both improve solubility and enhance cofacial interactions in the solid. We discuss the crystal packing of these materials, as well as their physical properties such as oxidation potential, UV-vis absorption, fluorescence emission, and decomposition pathways.",

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T1 - Stable, crystalline acenedithiophenes with up to seven linearly fused rings

AU - Payne, Marcia M.

AU - Odom, Susan A.

AU - Parkin, Sean R.

AU - Anthony, John E.

PY - 2004/9/16

Y1 - 2004/9/16

N2 - (Chemical Equation Presented) We report the synthesis of a series of crystalline acenedithiophenes with up to seven linearly fused rings and silylethynyl substituents. These functional groups are designed to both improve solubility and enhance cofacial interactions in the solid. We discuss the crystal packing of these materials, as well as their physical properties such as oxidation potential, UV-vis absorption, fluorescence emission, and decomposition pathways.

AB - (Chemical Equation Presented) We report the synthesis of a series of crystalline acenedithiophenes with up to seven linearly fused rings and silylethynyl substituents. These functional groups are designed to both improve solubility and enhance cofacial interactions in the solid. We discuss the crystal packing of these materials, as well as their physical properties such as oxidation potential, UV-vis absorption, fluorescence emission, and decomposition pathways.

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JO - Organic Letters

JF - Organic Letters

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ER -

Stable, crystalline acenedithiophenes with up to seven linearly fused rings

Abstract

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