Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanone

The title compound, C15H11NO4, crystallizes in two polymorphic forms, centrosymmetric monoclinic and chiral orthorhombic. The geometry of the molecules in the two polymorphs is slightly different, possibly due to intermolecular interactions. There are no classical hydrogen bonding in these two struc...

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Main Authors: Fred H. Greenberg, Alexander Y. Nazarenko
Format: Article
Language:English
Published: International Union of Crystallography 2016-07-01
Series:Acta Crystallographica Section E: Crystallographic Communications
Subjects:
Online Access:http://scripts.iucr.org/cgi-bin/paper?S2056989016010239
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author Fred H. Greenberg
Alexander Y. Nazarenko
author_facet Fred H. Greenberg
Alexander Y. Nazarenko
author_sort Fred H. Greenberg
collection DOAJ
description The title compound, C15H11NO4, crystallizes in two polymorphic forms, centrosymmetric monoclinic and chiral orthorhombic. The geometry of the molecules in the two polymorphs is slightly different, possibly due to intermolecular interactions. There are no classical hydrogen bonding in these two structures. However, a number of C—H...O intermolecular interactions, involving both O atoms of the nitro as well the benzoyl groups, stabilize the crystal structures.
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spelling doaj.art-1772f7e0d6ba427e812ba4732d910a632022-12-22T04:08:51ZengInternational Union of CrystallographyActa Crystallographica Section E: Crystallographic Communications2056-98902016-07-017271054105910.1107/S2056989016010239zl2667Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanoneFred H. Greenberg0Alexander Y. Nazarenko1Chemistry Department, SUNY Buffalo State, 1300 Elmwood Ave, Buffalo, NY 14222, USAChemistry Department, SUNY Buffalo State, 1300 Elmwood Ave, Buffalo, NY 14222, USAThe title compound, C15H11NO4, crystallizes in two polymorphic forms, centrosymmetric monoclinic and chiral orthorhombic. The geometry of the molecules in the two polymorphs is slightly different, possibly due to intermolecular interactions. There are no classical hydrogen bonding in these two structures. However, a number of C—H...O intermolecular interactions, involving both O atoms of the nitro as well the benzoyl groups, stabilize the crystal structures.http://scripts.iucr.org/cgi-bin/paper?S2056989016010239crystal structurechalcone oxidepolymorphism
spellingShingle Fred H. Greenberg
Alexander Y. Nazarenko
Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanone
Acta Crystallographica Section E: Crystallographic Communications
crystal structure
chalcone oxide
polymorphism
title Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanone
title_full Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanone
title_fullStr Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanone
title_full_unstemmed Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanone
title_short Two polymorphs of trans-[3-(3-nitrophenyl)oxiran-2-yl](phenyl)methanone
title_sort two polymorphs of trans 3 3 nitrophenyl oxiran 2 yl phenyl methanone
topic crystal structure
chalcone oxide
polymorphism
url http://scripts.iucr.org/cgi-bin/paper?S2056989016010239
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