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1-Benzyl-1H-benzotriazole
In the title compound, C(13)H(11)N(3), the benzotriazole ring system is essentially planar, with a maximum deviation of 0.0173 (18) Å, and forms a dihedral angle of 75.08 (8)Å with the phenyl ring. In the crystal, pairs of weak C—H⋯N hydrogen bonds form inversion dimers. In addition, there are weak...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344078/ https://www.ncbi.nlm.nih.gov/pubmed/22589987 http://dx.doi.org/10.1107/S1600536812010951 |
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author | Selvarathy Grace, P. Jebas, Samuel Robinson Ravindran Durai Nayagam, B. Schollmeyer, Dieter |
author_facet | Selvarathy Grace, P. Jebas, Samuel Robinson Ravindran Durai Nayagam, B. Schollmeyer, Dieter |
author_sort | Selvarathy Grace, P. |
collection | PubMed |
description | In the title compound, C(13)H(11)N(3), the benzotriazole ring system is essentially planar, with a maximum deviation of 0.0173 (18) Å, and forms a dihedral angle of 75.08 (8)Å with the phenyl ring. In the crystal, pairs of weak C—H⋯N hydrogen bonds form inversion dimers. In addition, there are weak C—H⋯π(arene) interactions and weak π–π stacking interactions, with a centroid–centroid distance of 3.673 (11) Å. |
format | Online Article Text |
id | pubmed-3344078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33440782012-05-15 1-Benzyl-1H-benzotriazole Selvarathy Grace, P. Jebas, Samuel Robinson Ravindran Durai Nayagam, B. Schollmeyer, Dieter Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(11)N(3), the benzotriazole ring system is essentially planar, with a maximum deviation of 0.0173 (18) Å, and forms a dihedral angle of 75.08 (8)Å with the phenyl ring. In the crystal, pairs of weak C—H⋯N hydrogen bonds form inversion dimers. In addition, there are weak C—H⋯π(arene) interactions and weak π–π stacking interactions, with a centroid–centroid distance of 3.673 (11) Å. International Union of Crystallography 2012-03-21 /pmc/articles/PMC3344078/ /pubmed/22589987 http://dx.doi.org/10.1107/S1600536812010951 Text en © Selvarathy Grace 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 Selvarathy Grace, P. Jebas, Samuel Robinson Ravindran Durai Nayagam, B. Schollmeyer, Dieter 1-Benzyl-1H-benzotriazole |
title | 1-Benzyl-1H-benzotriazole |
title_full | 1-Benzyl-1H-benzotriazole |
title_fullStr | 1-Benzyl-1H-benzotriazole |
title_full_unstemmed | 1-Benzyl-1H-benzotriazole |
title_short | 1-Benzyl-1H-benzotriazole |
title_sort | 1-benzyl-1h-benzotriazole |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344078/ https://www.ncbi.nlm.nih.gov/pubmed/22589987 http://dx.doi.org/10.1107/S1600536812010951 |
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