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N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide
The title compound, C(26)H(26)N(2)O(4), synthesized by the reaction of naphthalene-1,4,5,8-tetracarboxylic acid anhydride and cyclohexylamine, exhibits good n-type semiconducting properties. Accordingly, thin-film transistor devices comprising this compound show n-type behavior with high field-ef...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960487/ https://www.ncbi.nlm.nih.gov/pubmed/21201718 http://dx.doi.org/10.1107/S1600536808025221 |
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author | Shukla, Deepak Rajeswaran, Manju |
author_facet | Shukla, Deepak Rajeswaran, Manju |
author_sort | Shukla, Deepak |
collection | PubMed |
description | The title compound, C(26)H(26)N(2)O(4), synthesized by the reaction of naphthalene-1,4,5,8-tetracarboxylic acid anhydride and cyclohexylamine, exhibits good n-type semiconducting properties. Accordingly, thin-film transistor devices comprising this compound show n-type behavior with high field-effect electron moblity ca 6 cm(2)/Vs [Shukla, Nelson, Freeman, Rajeswaran, Ahearn, Meyer & Carey(2008 ▶). Chem. Mater. Submitted]. The asymmetric unit comprises one-quarter of the centrosymmetric molecule in which all but two methylene C atoms of the cyclohexane ring lie on a mirror plane; the point-group symmetry is 2/m. The naphthalenediimide unit is strictly planar, and the cyclohexane rings adopt chair conformations with the diimide unit in an equatorial position on each ring. |
format | Text |
id | pubmed-2960487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29604872010-12-30 N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide Shukla, Deepak Rajeswaran, Manju Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(26)H(26)N(2)O(4), synthesized by the reaction of naphthalene-1,4,5,8-tetracarboxylic acid anhydride and cyclohexylamine, exhibits good n-type semiconducting properties. Accordingly, thin-film transistor devices comprising this compound show n-type behavior with high field-effect electron moblity ca 6 cm(2)/Vs [Shukla, Nelson, Freeman, Rajeswaran, Ahearn, Meyer & Carey(2008 ▶). Chem. Mater. Submitted]. The asymmetric unit comprises one-quarter of the centrosymmetric molecule in which all but two methylene C atoms of the cyclohexane ring lie on a mirror plane; the point-group symmetry is 2/m. The naphthalenediimide unit is strictly planar, and the cyclohexane rings adopt chair conformations with the diimide unit in an equatorial position on each ring. International Union of Crystallography 2008-08-09 /pmc/articles/PMC2960487/ /pubmed/21201718 http://dx.doi.org/10.1107/S1600536808025221 Text en © Shukla and Rajeswaran 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Shukla, Deepak Rajeswaran, Manju N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide |
title |
N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide |
title_full |
N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide |
title_fullStr |
N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide |
title_full_unstemmed |
N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide |
title_short |
N,N′-Dicyclohexylnaphthalene-1,8;4:5-dicarboximide |
title_sort | n,n′-dicyclohexylnaphthalene-1,8;4:5-dicarboximide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960487/ https://www.ncbi.nlm.nih.gov/pubmed/21201718 http://dx.doi.org/10.1107/S1600536808025221 |
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