4′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione
In the title compound, C32H23FN2O3, the pyrrolidine ring adopts an envelope conformation. The monoketo- and diketo-substituted five-membered rings are in envelope and half-chair conformations, respectively. The molecular structure is stabilized by an intramolecular C—H...O hydrogen bon...
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International Union of Crystallography
2011-09-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536811032946 |
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doaj-95740ec26105429cb7736aeb33b2a5452020-11-25T01:13:22ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682011-09-01679o2381o238210.1107/S16005368110329464′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trioneAng Chee WeiMohamed Ashraf AliRusli IsmailChing Kheng QuahHoong-Kun FunIn the title compound, C32H23FN2O3, the pyrrolidine ring adopts an envelope conformation. The monoketo- and diketo-substituted five-membered rings are in envelope and half-chair conformations, respectively. The molecular structure is stabilized by an intramolecular C—H...O hydrogen bond, which generates an S(6) ring motif. In the crystal, molecules are linked via intermolecular C—H...N and C—H...O hydrogen bonds into a three-dimensional network. The crystal structure is further consolidated by C—H...π interactions.http://scripts.iucr.org/cgi-bin/paper?S1600536811032946 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ang Chee Wei Mohamed Ashraf Ali Rusli Ismail Ching Kheng Quah Hoong-Kun Fun |
spellingShingle |
Ang Chee Wei Mohamed Ashraf Ali Rusli Ismail Ching Kheng Quah Hoong-Kun Fun 4′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione Acta Crystallographica Section E |
author_facet |
Ang Chee Wei Mohamed Ashraf Ali Rusli Ismail Ching Kheng Quah Hoong-Kun Fun |
author_sort |
Ang Chee Wei |
title |
4′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_short |
4′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_full |
4′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_fullStr |
4′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_full_unstemmed |
4′-[5-(4-Fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_sort |
4′-[5-(4-fluorophenyl)pyridin-3-yl]-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2011-09-01 |
description |
In the title compound, C32H23FN2O3, the pyrrolidine ring adopts an envelope conformation. The monoketo- and diketo-substituted five-membered rings are in envelope and half-chair conformations, respectively. The molecular structure is stabilized by an intramolecular C—H...O hydrogen bond, which generates an S(6) ring motif. In the crystal, molecules are linked via intermolecular C—H...N and C—H...O hydrogen bonds into a three-dimensional network. The crystal structure is further consolidated by C—H...π interactions. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536811032946 |
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