Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: Crystal engineering of planar structures for p-type organic semiconductors

David J. Crouch; Peter J. Skabara; Martin Heeney; Iain McCulloch; Simon J. Coles; Michael B. Hursthouse

doi:10.1039/b417642a

Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: Crystal engineering of planar structures for p-type organic semiconductors

David J. Crouch
, Peter J. Skabara
, Martin Heeney
, Iain McCulloch
, Simon J. Coles
, Michael B. Hursthouse

Research output: Contribution to journal › Article › peer-review

66 Scopus citations

Abstract

Rigidification has been achieved in thiophene-tetrafluoro phenylene architectures through strong S⋯F and H⋯F intramolecular interactions; the resulting materials are promising candidates for p-type organic field effect transistors.

Original language	English (US)
Pages (from-to)	1465-1467
Number of pages	3
Journal	Chemical Communications
Issue number	11
DOIs	https://doi.org/10.1039/b417642a
State	Published - Mar 21 2005
Externally published	Yes

All Science Journal Classification (ASJC) codes

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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10.1039/b417642a

Cite this

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title = "Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: Crystal engineering of planar structures for p-type organic semiconductors",

abstract = "Rigidification has been achieved in thiophene-tetrafluoro phenylene architectures through strong S⋯F and H⋯F intramolecular interactions; the resulting materials are promising candidates for p-type organic field effect transistors.",

author = "Crouch, \{David J.\} and Skabara, \{Peter J.\} and Martin Heeney and Iain McCulloch and Coles, \{Simon J.\} and Hursthouse, \{Michael B.\}",

year = "2005",

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AU - Crouch, David J.

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AU - Heeney, Martin

AU - McCulloch, Iain

AU - Coles, Simon J.

AU - Hursthouse, Michael B.

PY - 2005/3/21

Y1 - 2005/3/21

N2 - Rigidification has been achieved in thiophene-tetrafluoro phenylene architectures through strong S⋯F and H⋯F intramolecular interactions; the resulting materials are promising candidates for p-type organic field effect transistors.

AB - Rigidification has been achieved in thiophene-tetrafluoro phenylene architectures through strong S⋯F and H⋯F intramolecular interactions; the resulting materials are promising candidates for p-type organic field effect transistors.

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UR - https://www.scopus.com/pages/publications/16444370557#tab=citedBy

U2 - 10.1039/b417642a

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JF - Chemical Communications

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Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: Crystal engineering of planar structures for p-type organic semiconductors

Abstract

All Science Journal Classification (ASJC) codes

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