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1,4,5,8-Tetraisopropylanthracene
The molecules of the title compound, C(26)H(34), possess crystallographically imposed inversion symmetry. The anthracene ring system is planar within 0.038 (1) Å. The two methyl groups in each independent isopropyl group are oriented on either side of the anthracene plane. In the crystal structure,...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008069/ https://www.ncbi.nlm.nih.gov/pubmed/21588593 http://dx.doi.org/10.1107/S1600536810030837 |
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author | Kitamura, Chitoshi Tsukuda, Hideki Kawase, Takeshi Kobayashi, Takashi Naito, Hiroyoshi |
author_facet | Kitamura, Chitoshi Tsukuda, Hideki Kawase, Takeshi Kobayashi, Takashi Naito, Hiroyoshi |
author_sort | Kitamura, Chitoshi |
collection | PubMed |
description | The molecules of the title compound, C(26)H(34), possess crystallographically imposed inversion symmetry. The anthracene ring system is planar within 0.038 (1) Å. The two methyl groups in each independent isopropyl group are oriented on either side of the anthracene plane. In the crystal structure, the molecules adopt a herringbone-like arrangement without π–π stacking. |
format | Text |
id | pubmed-3008069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30080692010-12-30 1,4,5,8-Tetraisopropylanthracene Kitamura, Chitoshi Tsukuda, Hideki Kawase, Takeshi Kobayashi, Takashi Naito, Hiroyoshi Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecules of the title compound, C(26)H(34), possess crystallographically imposed inversion symmetry. The anthracene ring system is planar within 0.038 (1) Å. The two methyl groups in each independent isopropyl group are oriented on either side of the anthracene plane. In the crystal structure, the molecules adopt a herringbone-like arrangement without π–π stacking. International Union of Crystallography 2010-08-11 /pmc/articles/PMC3008069/ /pubmed/21588593 http://dx.doi.org/10.1107/S1600536810030837 Text en © Kitamura et al. 2010 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 Kitamura, Chitoshi Tsukuda, Hideki Kawase, Takeshi Kobayashi, Takashi Naito, Hiroyoshi 1,4,5,8-Tetraisopropylanthracene |
title | 1,4,5,8-Tetraisopropylanthracene |
title_full | 1,4,5,8-Tetraisopropylanthracene |
title_fullStr | 1,4,5,8-Tetraisopropylanthracene |
title_full_unstemmed | 1,4,5,8-Tetraisopropylanthracene |
title_short | 1,4,5,8-Tetraisopropylanthracene |
title_sort | 1,4,5,8-tetraisopropylanthracene |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008069/ https://www.ncbi.nlm.nih.gov/pubmed/21588593 http://dx.doi.org/10.1107/S1600536810030837 |
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