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Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2)
In the title compound, C(5)H(9)NO(2)·2C(6)H(5)NO(3), the pyrrolidine ring of the pyrrolidinium-2-carboxylate zwitterion adopts a twisted conformation on the –CH(2)—CH(2)– bond adjacent to the N atom. The mean plane of this pyrrolidine ring forms dihedral angles of 25.3 (3) and 32.1 (3)° with the tw...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884369/ https://www.ncbi.nlm.nih.gov/pubmed/24454145 http://dx.doi.org/10.1107/S1600536813028742 |
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author | Sowmya, Narayanan Swarna Vidyalakshmi, Yechuri Sampathkrishnan, Sadasivam Srinivasan, Thothadri Velmurugan, Devadasan |
author_facet | Sowmya, Narayanan Swarna Vidyalakshmi, Yechuri Sampathkrishnan, Sadasivam Srinivasan, Thothadri Velmurugan, Devadasan |
author_sort | Sowmya, Narayanan Swarna |
collection | PubMed |
description | In the title compound, C(5)H(9)NO(2)·2C(6)H(5)NO(3), the pyrrolidine ring of the pyrrolidinium-2-carboxylate zwitterion adopts a twisted conformation on the –CH(2)—CH(2)– bond adjacent to the N atom. The mean plane of this pyrrolidine ring forms dihedral angles of 25.3 (3) and 32.1 (3)° with the two nitrophenol rings. An intramolecular N—H⋯O hydrogen bond occurs in the pyrrolidinium-2-carboxylate molecule. In the crystal, molecules are linked via O—H⋯O and N—H⋯O hydrogen bonds, enclosing R (3) (2)(8) ring motifs, forming chains running parallel to the a axis. These chains are further cross-linked by O—H⋯O and C—H⋯O hydrogen bonds, forming undulating two-dimensional networks lying parallel to (001). |
format | Online Article Text |
id | pubmed-3884369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-38843692014-01-17 Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) Sowmya, Narayanan Swarna Vidyalakshmi, Yechuri Sampathkrishnan, Sadasivam Srinivasan, Thothadri Velmurugan, Devadasan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(5)H(9)NO(2)·2C(6)H(5)NO(3), the pyrrolidine ring of the pyrrolidinium-2-carboxylate zwitterion adopts a twisted conformation on the –CH(2)—CH(2)– bond adjacent to the N atom. The mean plane of this pyrrolidine ring forms dihedral angles of 25.3 (3) and 32.1 (3)° with the two nitrophenol rings. An intramolecular N—H⋯O hydrogen bond occurs in the pyrrolidinium-2-carboxylate molecule. In the crystal, molecules are linked via O—H⋯O and N—H⋯O hydrogen bonds, enclosing R (3) (2)(8) ring motifs, forming chains running parallel to the a axis. These chains are further cross-linked by O—H⋯O and C—H⋯O hydrogen bonds, forming undulating two-dimensional networks lying parallel to (001). International Union of Crystallography 2013-10-31 /pmc/articles/PMC3884369/ /pubmed/24454145 http://dx.doi.org/10.1107/S1600536813028742 Text en © Sowmya et al. 2013 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 Sowmya, Narayanan Swarna Vidyalakshmi, Yechuri Sampathkrishnan, Sadasivam Srinivasan, Thothadri Velmurugan, Devadasan Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) |
title | Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) |
title_full | Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) |
title_fullStr | Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) |
title_full_unstemmed | Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) |
title_short | Pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) |
title_sort | pyrrolidinium-2-carboxylate–4-nitrophenol (1/2) |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884369/ https://www.ncbi.nlm.nih.gov/pubmed/24454145 http://dx.doi.org/10.1107/S1600536813028742 |
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