(E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine

In the crystal of the title compound, C16H16N2O3, weak C—H...O hydrogen bonds involving the nitro group as acceptor form chains extending in the b-axis direction. The chains are arranged into layers by π–π stacking interactions along the c-axis direction between the substituted pyridine rings, separ...

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Main Authors: Youness El Bakri, Youssef Ramli, Abdallah Harmaoui, Jihad Sebhaoui, El Mokhtar Essassi, Joel T. Mague
Format: Article
Language:English
Published: International Union of Crystallography 2016-12-01
Series:IUCrData
Subjects:
Online Access:http://scripts.iucr.org/cgi-bin/paper?S2414314616019660
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spelling doaj-12489c93143344cb8c8621f3506943012020-11-24T23:49:41ZengInternational Union of CrystallographyIUCrData2414-31462016-12-01112x16196610.1107/S2414314616019660bh4020(E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridineYouness El Bakri0Youssef Ramli1Abdallah Harmaoui2Jihad Sebhaoui3El Mokhtar Essassi4Joel T. Mague5Laboratoire de Chimie Organique Hétérocyclique, URAC 21, Pôle de Compétence Pharmacochimie, Av Ibn Battouta, BP 1014, Faculté des Sciences, Mohammed V University, Rabat, MoroccoMedicinal Chemistry Laboratory, Faculty of Medicine and Pharmacy, Mohammed V University in Rabat, 10170 Rabat, MoroccoLaboratoire de Chimie Organique Hétérocyclique, URAC 21, Pôle de Compétence Pharmacochimie, Av Ibn Battouta, BP 1014, Faculté des Sciences, Mohammed V University, Rabat, MoroccoLaboratoire de Chimie Organique Hétérocyclique, URAC 21, Pôle de Compétence Pharmacochimie, Av Ibn Battouta, BP 1014, Faculté des Sciences, Mohammed V University, Rabat, MoroccoLaboratoire de Chimie Organique Hétérocyclique, URAC 21, Pôle de Compétence Pharmacochimie, Av Ibn Battouta, BP 1014, Faculté des Sciences, Mohammed V University, Rabat, MoroccoDepartment of Chemistry, Tulane University, New Orleans, LA 70118, USAIn the crystal of the title compound, C16H16N2O3, weak C—H...O hydrogen bonds involving the nitro group as acceptor form chains extending in the b-axis direction. The chains are arranged into layers by π–π stacking interactions along the c-axis direction between the substituted pyridine rings, separated by 3.624 (1) Å.http://scripts.iucr.org/cgi-bin/paper?S2414314616019660crystal structurehydrogen bondπ–π stacking
collection DOAJ
language English
format Article
sources DOAJ
author Youness El Bakri
Youssef Ramli
Abdallah Harmaoui
Jihad Sebhaoui
El Mokhtar Essassi
Joel T. Mague
spellingShingle Youness El Bakri
Youssef Ramli
Abdallah Harmaoui
Jihad Sebhaoui
El Mokhtar Essassi
Joel T. Mague
(E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine
IUCrData
crystal structure
hydrogen bond
π–π stacking
author_facet Youness El Bakri
Youssef Ramli
Abdallah Harmaoui
Jihad Sebhaoui
El Mokhtar Essassi
Joel T. Mague
author_sort Youness El Bakri
title (E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine
title_short (E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine
title_full (E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine
title_fullStr (E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine
title_full_unstemmed (E)-4-Methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine
title_sort (e)-4-methoxy-3,5-dimethyl-2-[(3-nitrophenyl)ethenyl]pyridine
publisher International Union of Crystallography
series IUCrData
issn 2414-3146
publishDate 2016-12-01
description In the crystal of the title compound, C16H16N2O3, weak C—H...O hydrogen bonds involving the nitro group as acceptor form chains extending in the b-axis direction. The chains are arranged into layers by π–π stacking interactions along the c-axis direction between the substituted pyridine rings, separated by 3.624 (1) Å.
topic crystal structure
hydrogen bond
π–π stacking
url http://scripts.iucr.org/cgi-bin/paper?S2414314616019660
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