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(E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine
The complete molecule in the title compound, C(22)H(20)N(2)O(4), is generated by the application of an inversion centre. With the exception of the terminal acetylene groups [C—O—C—C = −78.02 (17)°], the remaining atoms constituting the molecule are essentially coplanar. The configuration around t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152067/ https://www.ncbi.nlm.nih.gov/pubmed/21837059 http://dx.doi.org/10.1107/S1600536811022410 |
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author | Al-Mehana, Wisam Naji Atiyah Shakir, Raied M. Yahya, Rosiyah Abd Halim, Siti Nadiah Tiekink, Edward R. T. |
author_facet | Al-Mehana, Wisam Naji Atiyah Shakir, Raied M. Yahya, Rosiyah Abd Halim, Siti Nadiah Tiekink, Edward R. T. |
author_sort | Al-Mehana, Wisam Naji Atiyah |
collection | PubMed |
description | The complete molecule in the title compound, C(22)H(20)N(2)O(4), is generated by the application of an inversion centre. With the exception of the terminal acetylene groups [C—O—C—C = −78.02 (17)°], the remaining atoms constituting the molecule are essentially coplanar. The configuration around the C=N bond [1.282 (2) Å] is E. The formation of supramolecular chains mediated by C—H⋯O interactions, occurring between methylene H and methoxy O atoms, is the most notable feature of the crystal packing. |
format | Online Article Text |
id | pubmed-3152067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-31520672011-08-11 (E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine Al-Mehana, Wisam Naji Atiyah Shakir, Raied M. Yahya, Rosiyah Abd Halim, Siti Nadiah Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete molecule in the title compound, C(22)H(20)N(2)O(4), is generated by the application of an inversion centre. With the exception of the terminal acetylene groups [C—O—C—C = −78.02 (17)°], the remaining atoms constituting the molecule are essentially coplanar. The configuration around the C=N bond [1.282 (2) Å] is E. The formation of supramolecular chains mediated by C—H⋯O interactions, occurring between methylene H and methoxy O atoms, is the most notable feature of the crystal packing. International Union of Crystallography 2011-06-18 /pmc/articles/PMC3152067/ /pubmed/21837059 http://dx.doi.org/10.1107/S1600536811022410 Text en © Al-Mehana et al. 2011 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 Al-Mehana, Wisam Naji Atiyah Shakir, Raied M. Yahya, Rosiyah Abd Halim, Siti Nadiah Tiekink, Edward R. T. (E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine |
title | (E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine |
title_full | (E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine |
title_fullStr | (E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine |
title_full_unstemmed | (E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine |
title_short | (E,E)-1,2-Bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine |
title_sort | (e,e)-1,2-bis[3-methoxy-4-(prop-2-yn-1-yloxy)benzylidene]hydrazine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152067/ https://www.ncbi.nlm.nih.gov/pubmed/21837059 http://dx.doi.org/10.1107/S1600536811022410 |
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