Cargando…
1,8-Diiodoanthracene
The molecule of the title compound, C(14)H(8)I(2), an intermediate in the synthesis of organic materials, is nearly planar, the maximum deviation from the mean plane being 0.032 (1) Å for the C atoms and 0.082 (2) Å for the I atoms. In the crystal structure, a sandwich–herringbone arrangement of m...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983297/ https://www.ncbi.nlm.nih.gov/pubmed/21587509 http://dx.doi.org/10.1107/S1600536810035191 |
_version_ | 1782191848012382208 |
---|---|
author | Nakanishi, Waka Hitosugi, Shunpei Piskareva, Anna Isobe, Hiroyuki |
author_facet | Nakanishi, Waka Hitosugi, Shunpei Piskareva, Anna Isobe, Hiroyuki |
author_sort | Nakanishi, Waka |
collection | PubMed |
description | The molecule of the title compound, C(14)H(8)I(2), an intermediate in the synthesis of organic materials, is nearly planar, the maximum deviation from the mean plane being 0.032 (1) Å for the C atoms and 0.082 (2) Å for the I atoms. In the crystal structure, a sandwich–herringbone arrangement of molecules is observed, whereas a columnar π-stacking arrangement has been reported for the chlorinated congener 1,8-dichloroanthracene. Similar effects of halogen substituents on the modulation of packing arrangements are reported for halogenated aromatic compounds such as tetracenes and chrycenes. |
format | Text |
id | pubmed-2983297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29832972010-12-30 1,8-Diiodoanthracene Nakanishi, Waka Hitosugi, Shunpei Piskareva, Anna Isobe, Hiroyuki Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecule of the title compound, C(14)H(8)I(2), an intermediate in the synthesis of organic materials, is nearly planar, the maximum deviation from the mean plane being 0.032 (1) Å for the C atoms and 0.082 (2) Å for the I atoms. In the crystal structure, a sandwich–herringbone arrangement of molecules is observed, whereas a columnar π-stacking arrangement has been reported for the chlorinated congener 1,8-dichloroanthracene. Similar effects of halogen substituents on the modulation of packing arrangements are reported for halogenated aromatic compounds such as tetracenes and chrycenes. International Union of Crystallography 2010-09-08 /pmc/articles/PMC2983297/ /pubmed/21587509 http://dx.doi.org/10.1107/S1600536810035191 Text en © Nakanishi 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 Nakanishi, Waka Hitosugi, Shunpei Piskareva, Anna Isobe, Hiroyuki 1,8-Diiodoanthracene |
title | 1,8-Diiodoanthracene |
title_full | 1,8-Diiodoanthracene |
title_fullStr | 1,8-Diiodoanthracene |
title_full_unstemmed | 1,8-Diiodoanthracene |
title_short | 1,8-Diiodoanthracene |
title_sort | 1,8-diiodoanthracene |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983297/ https://www.ncbi.nlm.nih.gov/pubmed/21587509 http://dx.doi.org/10.1107/S1600536810035191 |
work_keys_str_mv | AT nakanishiwaka 18diiodoanthracene AT hitosugishunpei 18diiodoanthracene AT piskarevaanna 18diiodoanthracene AT isobehiroyuki 18diiodoanthracene |