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2,3-Bis(4-ethoxyphenyl)quinoxaline
The title compound, C(24)H(22)N(2)O(2), was prepared by condensation of 1,2-bis(4-ethoxyphenyl)ethane-1,2-dione and 1,2-diaminobenzene. The asymmetric unit contains one half-molecule, close to a twofold axis. The plane of the quinoxaline ring is twisted with respect to the planes of the two eth...
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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/PMC2980160/ https://www.ncbi.nlm.nih.gov/pubmed/21580021 http://dx.doi.org/10.1107/S1600536809052295 |
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author | Ye, Ping-Ping Zhang, Cai-Li Du, Zhi-Qiang |
author_facet | Ye, Ping-Ping Zhang, Cai-Li Du, Zhi-Qiang |
author_sort | Ye, Ping-Ping |
collection | PubMed |
description | The title compound, C(24)H(22)N(2)O(2), was prepared by condensation of 1,2-bis(4-ethoxyphenyl)ethane-1,2-dione and 1,2-diaminobenzene. The asymmetric unit contains one half-molecule, close to a twofold axis. The plane of the quinoxaline ring is twisted with respect to the planes of the two ethoxyphenyl ring systems, exhibiting dihedral angles of 39.95 (9)°. The crystal packing is dominated by weak C—H⋯π interactions. No classical hydrogen bonds or stacking interactions are observed. |
format | Text |
id | pubmed-2980160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29801602010-12-30 2,3-Bis(4-ethoxyphenyl)quinoxaline Ye, Ping-Ping Zhang, Cai-Li Du, Zhi-Qiang Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(22)N(2)O(2), was prepared by condensation of 1,2-bis(4-ethoxyphenyl)ethane-1,2-dione and 1,2-diaminobenzene. The asymmetric unit contains one half-molecule, close to a twofold axis. The plane of the quinoxaline ring is twisted with respect to the planes of the two ethoxyphenyl ring systems, exhibiting dihedral angles of 39.95 (9)°. The crystal packing is dominated by weak C—H⋯π interactions. No classical hydrogen bonds or stacking interactions are observed. International Union of Crystallography 2009-12-12 /pmc/articles/PMC2980160/ /pubmed/21580021 http://dx.doi.org/10.1107/S1600536809052295 Text en © Ye 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 Ye, Ping-Ping Zhang, Cai-Li Du, Zhi-Qiang 2,3-Bis(4-ethoxyphenyl)quinoxaline |
title | 2,3-Bis(4-ethoxyphenyl)quinoxaline |
title_full | 2,3-Bis(4-ethoxyphenyl)quinoxaline |
title_fullStr | 2,3-Bis(4-ethoxyphenyl)quinoxaline |
title_full_unstemmed | 2,3-Bis(4-ethoxyphenyl)quinoxaline |
title_short | 2,3-Bis(4-ethoxyphenyl)quinoxaline |
title_sort | 2,3-bis(4-ethoxyphenyl)quinoxaline |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980160/ https://www.ncbi.nlm.nih.gov/pubmed/21580021 http://dx.doi.org/10.1107/S1600536809052295 |
work_keys_str_mv | AT yepingping 23bis4ethoxyphenylquinoxaline AT zhangcaili 23bis4ethoxyphenylquinoxaline AT duzhiqiang 23bis4ethoxyphenylquinoxaline |