Cargando…
2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile
In the title compound, C(16)H(13)IN(2), the two benzene rings make a dihedral angle of 67.26 (5)°. The six-membered heterocycle of the tetrahydroisoquinoline unit adopts a half-chair conformation. In the crystal, adjacent molecules are linked by pairs of weak intermolecular C—H⋯N hydrogen bonds,...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120457/ https://www.ncbi.nlm.nih.gov/pubmed/21754853 http://dx.doi.org/10.1107/S1600536811015212 |
_version_ | 1782206683688206336 |
---|---|
author | Ma, Yanni Sun, Yifang Zheng, Feng Sun, Wenwen Zhou, Le |
author_facet | Ma, Yanni Sun, Yifang Zheng, Feng Sun, Wenwen Zhou, Le |
author_sort | Ma, Yanni |
collection | PubMed |
description | In the title compound, C(16)H(13)IN(2), the two benzene rings make a dihedral angle of 67.26 (5)°. The six-membered heterocycle of the tetrahydroisoquinoline unit adopts a half-chair conformation. In the crystal, adjacent molecules are linked by pairs of weak intermolecular C—H⋯N hydrogen bonds, forming inversion dimers. An intramolecular C—H⋯I close contact is also observed. |
format | Online Article Text |
id | pubmed-3120457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-31204572011-07-13 2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile Ma, Yanni Sun, Yifang Zheng, Feng Sun, Wenwen Zhou, Le Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(13)IN(2), the two benzene rings make a dihedral angle of 67.26 (5)°. The six-membered heterocycle of the tetrahydroisoquinoline unit adopts a half-chair conformation. In the crystal, adjacent molecules are linked by pairs of weak intermolecular C—H⋯N hydrogen bonds, forming inversion dimers. An intramolecular C—H⋯I close contact is also observed. International Union of Crystallography 2011-05-20 /pmc/articles/PMC3120457/ /pubmed/21754853 http://dx.doi.org/10.1107/S1600536811015212 Text en © Ma 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 Ma, Yanni Sun, Yifang Zheng, Feng Sun, Wenwen Zhou, Le 2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile |
title | 2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile |
title_full | 2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile |
title_fullStr | 2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile |
title_full_unstemmed | 2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile |
title_short | 2-(2-Iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile |
title_sort | 2-(2-iodophenyl)-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120457/ https://www.ncbi.nlm.nih.gov/pubmed/21754853 http://dx.doi.org/10.1107/S1600536811015212 |
work_keys_str_mv | AT mayanni 22iodophenyl1234tetrahydroisoquinoline1carbonitrile AT sunyifang 22iodophenyl1234tetrahydroisoquinoline1carbonitrile AT zhengfeng 22iodophenyl1234tetrahydroisoquinoline1carbonitrile AT sunwenwen 22iodophenyl1234tetrahydroisoquinoline1carbonitrile AT zhoule 22iodophenyl1234tetrahydroisoquinoline1carbonitrile |