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6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine

In the title compound, C(24)H(20)N(4), obtained through the condensation of naphthalene-2,3-diamine with formaldehyde in methanol, the mol­ecule is located on a special position of site symmetry -4. Due to symmetry considerations, the aromatic rings are strictly perpendicular to each other. In the c...

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Detalles Bibliográficos
Autores principales: Rivera, Augusto, Maldonado, Mauricio, Ríos-Motta, Jaime, Fejfarová, Karla, Dušek, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344019/
https://www.ncbi.nlm.nih.gov/pubmed/22589928
http://dx.doi.org/10.1107/S1600536812010185
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author Rivera, Augusto
Maldonado, Mauricio
Ríos-Motta, Jaime
Fejfarová, Karla
Dušek, Michal
author_facet Rivera, Augusto
Maldonado, Mauricio
Ríos-Motta, Jaime
Fejfarová, Karla
Dušek, Michal
author_sort Rivera, Augusto
collection PubMed
description In the title compound, C(24)H(20)N(4), obtained through the condensation of naphthalene-2,3-diamine with formaldehyde in methanol, the mol­ecule is located on a special position of site symmetry -4. Due to symmetry considerations, the aromatic rings are strictly perpendicular to each other. In the crystal, mol­ecules are linked by pairs of C—H⋯π inter­actions into columns along [110].
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spelling pubmed-33440192012-05-15 6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine Rivera, Augusto Maldonado, Mauricio Ríos-Motta, Jaime Fejfarová, Karla Dušek, Michal Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(24)H(20)N(4), obtained through the condensation of naphthalene-2,3-diamine with formaldehyde in methanol, the mol­ecule is located on a special position of site symmetry -4. Due to symmetry considerations, the aromatic rings are strictly perpendicular to each other. In the crystal, mol­ecules are linked by pairs of C—H⋯π inter­actions into columns along [110]. International Union of Crystallography 2012-03-14 /pmc/articles/PMC3344019/ /pubmed/22589928 http://dx.doi.org/10.1107/S1600536812010185 Text en © Rivera et al. 2012 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
Rivera, Augusto
Maldonado, Mauricio
Ríos-Motta, Jaime
Fejfarová, Karla
Dušek, Michal
6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine
title 6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine
title_full 6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine
title_fullStr 6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine
title_full_unstemmed 6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine
title_short 6H,13H-5,12:7,14-Dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine
title_sort 6h,13h-5,12:7,14-dimethano­dinaphtho­[2,3-d:2,3-i][1,3,6,8]tetra­azecine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344019/
https://www.ncbi.nlm.nih.gov/pubmed/22589928
http://dx.doi.org/10.1107/S1600536812010185
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