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4-Bromoselenoanisole
The title compound, 1-bromo-4-methylselenobenzene, C(7)H(7)BrSe, was prepared by methylation of 4-bromoselenophenolate with methyl iodide, and crystals suitable for structure determination were obtained by sublimation. The molecule is essentially planar; the Se—Me bond is rotated by only 2.59 ...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969389/ https://www.ncbi.nlm.nih.gov/pubmed/21582926 http://dx.doi.org/10.1107/S160053680902296X |
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author | Sørensen, Henning Osholm Stuhr-Hansen, Nicolai |
author_facet | Sørensen, Henning Osholm Stuhr-Hansen, Nicolai |
author_sort | Sørensen, Henning Osholm |
collection | PubMed |
description | The title compound, 1-bromo-4-methylselenobenzene, C(7)H(7)BrSe, was prepared by methylation of 4-bromoselenophenolate with methyl iodide, and crystals suitable for structure determination were obtained by sublimation. The molecule is essentially planar; the Se—Me bond is rotated by only 2.59 (19)° out of the least-squares plane of the benzene ring. The most pronounced intermolecular interactions are two hydrogen bonds of the type C—H⋯π, which determine a herring-bone pattern in the crystal packing. |
format | Text |
id | pubmed-2969389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29693892010-12-30 4-Bromoselenoanisole Sørensen, Henning Osholm Stuhr-Hansen, Nicolai Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, 1-bromo-4-methylselenobenzene, C(7)H(7)BrSe, was prepared by methylation of 4-bromoselenophenolate with methyl iodide, and crystals suitable for structure determination were obtained by sublimation. The molecule is essentially planar; the Se—Me bond is rotated by only 2.59 (19)° out of the least-squares plane of the benzene ring. The most pronounced intermolecular interactions are two hydrogen bonds of the type C—H⋯π, which determine a herring-bone pattern in the crystal packing. International Union of Crystallography 2009-06-24 /pmc/articles/PMC2969389/ /pubmed/21582926 http://dx.doi.org/10.1107/S160053680902296X Text en © Sørensen and Stuhr-Hansen 2009 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 Sørensen, Henning Osholm Stuhr-Hansen, Nicolai 4-Bromoselenoanisole |
title | 4-Bromoselenoanisole |
title_full | 4-Bromoselenoanisole |
title_fullStr | 4-Bromoselenoanisole |
title_full_unstemmed | 4-Bromoselenoanisole |
title_short | 4-Bromoselenoanisole |
title_sort | 4-bromoselenoanisole |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969389/ https://www.ncbi.nlm.nih.gov/pubmed/21582926 http://dx.doi.org/10.1107/S160053680902296X |
work_keys_str_mv | AT sørensenhenningosholm 4bromoselenoanisole AT stuhrhansennicolai 4bromoselenoanisole |