2-Amino-5-bromopyridinium hydrogen succinate
In the title compound, C5H6BrN2+·C4H5O4−, the pyridine N atom of the 2-amino-5-bromopyridine molecule is protonated. The protonated N atom and the amino group are linked via N—H...O hydrogen bonds to the carboxylate O atoms of the singly deprotonated succinat...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2010-03-01
|
| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536810006495 |
| _version_ | 1818918630726828032 |
|---|---|
| author | Hoong-Kun Fun Madhukar Hemamalini |
| author_facet | Hoong-Kun Fun Madhukar Hemamalini |
| author_sort | Hoong-Kun Fun |
| collection | DOAJ |
| description | In the title compound, C5H6BrN2+·C4H5O4−, the pyridine N atom of the 2-amino-5-bromopyridine molecule is protonated. The protonated N atom and the amino group are linked via N—H...O hydrogen bonds to the carboxylate O atoms of the singly deprotonated succinate anion. The hydrogen succinate anions are linked via O—H...O hydrogen bonds. A weak intermolecular C—H...O hydrogen bond is also observed. |
| first_indexed | 2024-12-20T00:53:01Z |
| format | Article |
| id | doaj.art-07ef200fd77a4d5f8614a13b3fbd18fb |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-20T00:53:01Z |
| publishDate | 2010-03-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-07ef200fd77a4d5f8614a13b3fbd18fb2022-12-21T19:59:10ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-03-01663o689o69010.1107/S16005368100064952-Amino-5-bromopyridinium hydrogen succinateHoong-Kun FunMadhukar HemamaliniIn the title compound, C5H6BrN2+·C4H5O4−, the pyridine N atom of the 2-amino-5-bromopyridine molecule is protonated. The protonated N atom and the amino group are linked via N—H...O hydrogen bonds to the carboxylate O atoms of the singly deprotonated succinate anion. The hydrogen succinate anions are linked via O—H...O hydrogen bonds. A weak intermolecular C—H...O hydrogen bond is also observed.http://scripts.iucr.org/cgi-bin/paper?S1600536810006495 |
| spellingShingle | Hoong-Kun Fun Madhukar Hemamalini 2-Amino-5-bromopyridinium hydrogen succinate Acta Crystallographica Section E |
| title | 2-Amino-5-bromopyridinium hydrogen succinate |
| title_full | 2-Amino-5-bromopyridinium hydrogen succinate |
| title_fullStr | 2-Amino-5-bromopyridinium hydrogen succinate |
| title_full_unstemmed | 2-Amino-5-bromopyridinium hydrogen succinate |
| title_short | 2-Amino-5-bromopyridinium hydrogen succinate |
| title_sort | 2 amino 5 bromopyridinium hydrogen succinate |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536810006495 |
| work_keys_str_mv | AT hoongkunfun 2amino5bromopyridiniumhydrogensuccinate AT madhukarhemamalini 2amino5bromopyridiniumhydrogensuccinate |