1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole

The complete molecule of the title compound, C(24)H(24)N(6)O(2), is generated by a crystallographic inversion centre. The benzotriazole rings form dihedral angles of 2.10 (7)° with the central aromatic ring. The crystal packing is consolidated by π–π inter­actions, with centroid–centroid distances o...

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Detalles Bibliográficos
Autores principales: Ravindran Durai Nayagam, B., Jebas, Samuel Robinson, Daisy, Caroline, Schollmeyer, Dieter
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969066/
https://www.ncbi.nlm.nih.gov/pubmed/21582620
http://dx.doi.org/10.1107/S1600536809010782
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author Ravindran Durai Nayagam, B.
Jebas, Samuel Robinson
Daisy, Caroline
Schollmeyer, Dieter
author_facet Ravindran Durai Nayagam, B.
Jebas, Samuel Robinson
Daisy, Caroline
Schollmeyer, Dieter
author_sort Ravindran Durai Nayagam, B.
collection PubMed
description The complete molecule of the title compound, C(24)H(24)N(6)O(2), is generated by a crystallographic inversion centre. The benzotriazole rings form dihedral angles of 2.10 (7)° with the central aromatic ring. The crystal packing is consolidated by π–π inter­actions, with centroid–centroid distances of 3.6234 (10) Å, together with weak C—H⋯π inter­actions.
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spelling pubmed-29690662010-12-30 1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole Ravindran Durai Nayagam, B. Jebas, Samuel Robinson Daisy, Caroline Schollmeyer, Dieter Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete molecule of the title compound, C(24)H(24)N(6)O(2), is generated by a crystallographic inversion centre. The benzotriazole rings form dihedral angles of 2.10 (7)° with the central aromatic ring. The crystal packing is consolidated by π–π inter­actions, with centroid–centroid distances of 3.6234 (10) Å, together with weak C—H⋯π inter­actions. International Union of Crystallography 2009-03-28 /pmc/articles/PMC2969066/ /pubmed/21582620 http://dx.doi.org/10.1107/S1600536809010782 Text en © Ravindran Durai Nayagam et al. 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
Ravindran Durai Nayagam, B.
Jebas, Samuel Robinson
Daisy, Caroline
Schollmeyer, Dieter
1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole
title 1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole
title_full 1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole
title_fullStr 1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole
title_full_unstemmed 1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole
title_short 1,1′-[2,3,5,6-Tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1H-benzotriazole
title_sort 1,1′-[2,3,5,6-tetra­methyl-p-phenyl­ene­bis(methyl­eneoxy)]di-1h-benzotriazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969066/
https://www.ncbi.nlm.nih.gov/pubmed/21582620
http://dx.doi.org/10.1107/S1600536809010782
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