3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one
The conformation of the title molecule, C16H12N2O3, is partly determined by an intramolecular C=O...π interaction between one carbonyl group and the five-membered ring of the other indolinone moiety. The crystal packing consists of layers parallel to (001) formed by a combination of N—H...O and O—H....
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International Union of Crystallography
2017-02-01
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| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S2414314617001390 |
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doaj-a2906c0a302d4118bd7475dd377143512020-11-24T23:21:33ZengInternational Union of CrystallographyIUCrData2414-31462017-02-0122x17013910.1107/S2414314617001390sj40853-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-oneJoel T. Mague0Shaaban K. Mohamed1Mehmet Akkurt2Mohamed Shaker S. Adam3Farouq E. Hawaiz4Department of Chemistry, Tulane University, New Orleans, LA 70118, USAChemistry and Environmental Division, Manchester Metropolitan University, Manchester M1 5GD, EnglandDepartment of Physics, Faculty of Sciences, Erciyes University, 38039 Kayseri, TurkeyChemistry Department, Faculty of Science, Sohag University, Sohag-82534, EgyptChemistry Department, College of Education, Salahaddin University-Hawler, Erbil, Kurdistan Region, IraqThe conformation of the title molecule, C16H12N2O3, is partly determined by an intramolecular C=O...π interaction between one carbonyl group and the five-membered ring of the other indolinone moiety. The crystal packing consists of layers parallel to (001) formed by a combination of N—H...O and O—H...O hydrogen bonds and π–π stacking interactions. Both the N—H...O and O—H...O hydrogen bonds generate inversion dimers.http://scripts.iucr.org/cgi-bin/paper?S2414314617001390crystal structurehydrogen bondπ–π stackingindolinoneisatindimerization |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
Joel T. Mague Shaaban K. Mohamed Mehmet Akkurt Mohamed Shaker S. Adam Farouq E. Hawaiz |
| spellingShingle |
Joel T. Mague Shaaban K. Mohamed Mehmet Akkurt Mohamed Shaker S. Adam Farouq E. Hawaiz 3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one IUCrData crystal structure hydrogen bond π–π stacking indolinone isatin dimerization |
| author_facet |
Joel T. Mague Shaaban K. Mohamed Mehmet Akkurt Mohamed Shaker S. Adam Farouq E. Hawaiz |
| author_sort |
Joel T. Mague |
| title |
3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one |
| title_short |
3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one |
| title_full |
3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one |
| title_fullStr |
3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one |
| title_full_unstemmed |
3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one |
| title_sort |
3-hydroxy-3-(2-oxo-2,3-dihydro-1h-indol-3-yl)-2,3-dihydro-1h-indol-2-one |
| publisher |
International Union of Crystallography |
| series |
IUCrData |
| issn |
2414-3146 |
| publishDate |
2017-02-01 |
| description |
The conformation of the title molecule, C16H12N2O3, is partly determined by an intramolecular C=O...π interaction between one carbonyl group and the five-membered ring of the other indolinone moiety. The crystal packing consists of layers parallel to (001) formed by a combination of N—H...O and O—H...O hydrogen bonds and π–π stacking interactions. Both the N—H...O and O—H...O hydrogen bonds generate inversion dimers. |
| topic |
crystal structure hydrogen bond π–π stacking indolinone isatin dimerization |
| url |
http://scripts.iucr.org/cgi-bin/paper?S2414314617001390 |
| work_keys_str_mv |
AT joeltmague 3hydroxy32oxo23dihydro1hindol3yl23dihydro1hindol2one AT shaabankmohamed 3hydroxy32oxo23dihydro1hindol3yl23dihydro1hindol2one AT mehmetakkurt 3hydroxy32oxo23dihydro1hindol3yl23dihydro1hindol2one AT mohamedshakersadam 3hydroxy32oxo23dihydro1hindol3yl23dihydro1hindol2one AT farouqehawaiz 3hydroxy32oxo23dihydro1hindol3yl23dihydro1hindol2one |
| _version_ |
1725571325353787392 |