1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry

The title compound, C13H19NO8, is based on a tetra-substituted pyrrolidine ring, which has a twisted conformation about the central C—C bond; the Cm—Ca—Ca—Cme torsion angle is 38.26 (15)° [m = methyl­carboxyl­ate, a = acet­yloxy and me = methyl­ene]. While the N-bound ethyl­carboxyl­ate group occupi...

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Main Authors: Dallasta Pedroso, Sofia, Caracelli, Ignez, Zukerman-Schpector, Julio, Soto-Monsalve, Monica, De Almeida Santos, Regina H., Correia, Carlos Roque D., Llanes Garcia, A. L., Kwong, Huey Chong *, Tiekink, Edward R. T. *
Format: Article
Language:English
Published: International Union of Crystallography 2020
Subjects:
Online Access:http://eprints.sunway.edu.my/1297/
http://eprints.sunway.edu.my/1297/1/Tiekink%20Acta%20Cryst%202020%20E76%20967.pdf
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author Dallasta Pedroso, Sofia
Caracelli, Ignez
Zukerman-Schpector, Julio
Soto-Monsalve, Monica
De Almeida Santos, Regina H.
Correia, Carlos Roque D.
Llanes Garcia, A. L.
Kwong, Huey Chong *
Tiekink, Edward R. T. *
author_facet Dallasta Pedroso, Sofia
Caracelli, Ignez
Zukerman-Schpector, Julio
Soto-Monsalve, Monica
De Almeida Santos, Regina H.
Correia, Carlos Roque D.
Llanes Garcia, A. L.
Kwong, Huey Chong *
Tiekink, Edward R. T. *
author_sort Dallasta Pedroso, Sofia
building SU Institutional Repository
collection Online Access
description The title compound, C13H19NO8, is based on a tetra-substituted pyrrolidine ring, which has a twisted conformation about the central C—C bond; the Cm—Ca—Ca—Cme torsion angle is 38.26 (15)° [m = methyl­carboxyl­ate, a = acet­yloxy and me = methyl­ene]. While the N-bound ethyl­carboxyl­ate group occupies an equatorial position, the remaining substituents occupy axial positions. In the crystal, supra­molecular double-layers are formed by weak methyl- and methyl­ene-C—H...O(carbon­yl) inter­actions involving all four carbonyl-O atoms. The two-dimensional arrays stack along the c axis without directional inter­actions between them. The Hirshfeld surface is dominated by H...H (55.7%) and H...C/C...H (37.0%) contacts; H...H contacts are noted in the inter-double-layer region. The inter­action energy calculations point to the importance of the dispersion energy term in the stabilization of the crystal.
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language English
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publisher International Union of Crystallography
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spelling sunway-12972020-10-07T07:03:30Z http://eprints.sunway.edu.my/1297/ 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry Dallasta Pedroso, Sofia Caracelli, Ignez Zukerman-Schpector, Julio Soto-Monsalve, Monica De Almeida Santos, Regina H. Correia, Carlos Roque D. Llanes Garcia, A. L. Kwong, Huey Chong * Tiekink, Edward R. T. * QD Chemistry The title compound, C13H19NO8, is based on a tetra-substituted pyrrolidine ring, which has a twisted conformation about the central C—C bond; the Cm—Ca—Ca—Cme torsion angle is 38.26 (15)° [m = methyl­carboxyl­ate, a = acet­yloxy and me = methyl­ene]. While the N-bound ethyl­carboxyl­ate group occupies an equatorial position, the remaining substituents occupy axial positions. In the crystal, supra­molecular double-layers are formed by weak methyl- and methyl­ene-C—H...O(carbon­yl) inter­actions involving all four carbonyl-O atoms. The two-dimensional arrays stack along the c axis without directional inter­actions between them. The Hirshfeld surface is dominated by H...H (55.7%) and H...C/C...H (37.0%) contacts; H...H contacts are noted in the inter-double-layer region. The inter­action energy calculations point to the importance of the dispersion energy term in the stabilization of the crystal. International Union of Crystallography 2020-05-24 Article PeerReviewed text en cc_by_nc_4 http://eprints.sunway.edu.my/1297/1/Tiekink%20Acta%20Cryst%202020%20E76%20967.pdf Dallasta Pedroso, Sofia and Caracelli, Ignez and Zukerman-Schpector, Julio and Soto-Monsalve, Monica and De Almeida Santos, Regina H. and Correia, Carlos Roque D. and Llanes Garcia, A. L. and Kwong, Huey Chong * and Tiekink, Edward R. T. * (2020) 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry. Acta Crystallographica Section E Crystallographic Communications, 76 (6). pp. 967-972. ISSN 2056-9890 http://doi.org/10.1107/S205698902000701X doi:10.1107/S205698902000701X
spellingShingle QD Chemistry
Dallasta Pedroso, Sofia
Caracelli, Ignez
Zukerman-Schpector, Julio
Soto-Monsalve, Monica
De Almeida Santos, Regina H.
Correia, Carlos Roque D.
Llanes Garcia, A. L.
Kwong, Huey Chong *
Tiekink, Edward R. T. *
1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry
title 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry
title_full 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry
title_fullStr 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry
title_full_unstemmed 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry
title_short 1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry
title_sort 1-ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, hirshfeld surface analysis and computational chemistry
topic QD Chemistry
url http://eprints.sunway.edu.my/1297/
http://eprints.sunway.edu.my/1297/
http://eprints.sunway.edu.my/1297/
http://eprints.sunway.edu.my/1297/1/Tiekink%20Acta%20Cryst%202020%20E76%20967.pdf