3-(4-Chlorobutyl)-3H-indole-5-carbonitrile

3-(4-Chlorobutyl)-3H-indole-5-carbonitrile

In the title compound, C13H12ClN2, the indole moiety and the chloroalkyl substituent are nearly coplanar, making a dihedral angle of 1.27 (10)°. In the crystal, a supramolecular sheet parallel to the ab plane is generated via weak C—H...Cl hydrogen bonds, aromatic π–π stacking [centroid–centroid dis...

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Main Authors: Devakumar Manikandan, Sundaramoorthy Gomathi, Jeyaraman Selvaraj Nirmalram, Sadasivam Sharmila Tagore, Velusamy Sethuraman, Joseph Agim, Ray Butcher
Format: Article
Language:English
Published: International Union of Crystallography 2017-03-01
Series:IUCrData
Subjects:
crystal structure
3-(4-chlorobutyl)-3H-indole-5-carbonitrile,non-covalent interactions
supramolecular sheet
Online Access:http://scripts.iucr.org/cgi-bin/paper?S2414314617003765
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spelling doaj-ba70aebf862e462a96972c316eda48732020-11-25T02:04:22ZengInternational Union of CrystallographyIUCrData2414-31462017-03-0123x17037610.1107/S2414314617003765hg40203-(4-Chlorobutyl)-3H-indole-5-carbonitrileDevakumar Manikandan0Sundaramoorthy Gomathi1Jeyaraman Selvaraj Nirmalram2Sadasivam Sharmila Tagore3Velusamy Sethuraman4Joseph Agim5Ray Butcher6Department of Chemistry, Periyar Maniammai University, Thanjavur 613 403, Tamil Nadu, IndiaDepartment of Chemistry, Periyar Maniammai University, Thanjavur 613 403, Tamil Nadu, IndiaCentre for Research and Development, PRIST University, Thanjavur 613 403, Tamil Nadu, IndiaDepartment of Chemistry, Periyar Maniammai University, Thanjavur 613 403, Tamil Nadu, IndiaDepartment of Chemistry, Periyar Maniammai University, Thanjavur 613 403, Tamil Nadu, IndiaInorganic & Structural Chemistry, Howard University, Washington, DC 20059, USAInorganic & Structural Chemistry, Howard University, Washington, DC 20059, USAIn the title compound, C13H12ClN2, the indole moiety and the chloroalkyl substituent are nearly coplanar, making a dihedral angle of 1.27 (10)°. In the crystal, a supramolecular sheet parallel to the ab plane is generated via weak C—H...Cl hydrogen bonds, aromatic π–π stacking [centroid–centroid distances of 3.5563 (13) and 3.6792 (13) Å] and C—H...π interactions.http://scripts.iucr.org/cgi-bin/paper?S2414314617003765crystal structure3-(4-chlorobutyl)-3H-indole-5-carbonitrile,non-covalent interactionssupramolecular sheet
collection DOAJ
language English
format Article
sources DOAJ
author Devakumar Manikandan
Sundaramoorthy Gomathi
Jeyaraman Selvaraj Nirmalram
Sadasivam Sharmila Tagore
Velusamy Sethuraman
Joseph Agim
Ray Butcher
spellingShingle Devakumar Manikandan
Sundaramoorthy Gomathi
Jeyaraman Selvaraj Nirmalram
Sadasivam Sharmila Tagore
Velusamy Sethuraman
Joseph Agim
Ray Butcher
3-(4-Chlorobutyl)-3H-indole-5-carbonitrile
IUCrData
crystal structure
3-(4-chlorobutyl)-3H-indole-5-carbonitrile,non-covalent interactions
supramolecular sheet
author_facet Devakumar Manikandan
Sundaramoorthy Gomathi
Jeyaraman Selvaraj Nirmalram
Sadasivam Sharmila Tagore
Velusamy Sethuraman
Joseph Agim
Ray Butcher
author_sort Devakumar Manikandan
title 3-(4-Chlorobutyl)-3H-indole-5-carbonitrile
title_short 3-(4-Chlorobutyl)-3H-indole-5-carbonitrile
title_full 3-(4-Chlorobutyl)-3H-indole-5-carbonitrile
title_fullStr 3-(4-Chlorobutyl)-3H-indole-5-carbonitrile
title_full_unstemmed 3-(4-Chlorobutyl)-3H-indole-5-carbonitrile
title_sort 3-(4-chlorobutyl)-3h-indole-5-carbonitrile
publisher International Union of Crystallography
series IUCrData
issn 2414-3146
publishDate 2017-03-01
description In the title compound, C13H12ClN2, the indole moiety and the chloroalkyl substituent are nearly coplanar, making a dihedral angle of 1.27 (10)°. In the crystal, a supramolecular sheet parallel to the ab plane is generated via weak C—H...Cl hydrogen bonds, aromatic π–π stacking [centroid–centroid distances of 3.5563 (13) and 3.6792 (13) Å] and C—H...π interactions.
topic crystal structure
3-(4-chlorobutyl)-3H-indole-5-carbonitrile,non-covalent interactions
supramolecular sheet
url http://scripts.iucr.org/cgi-bin/paper?S2414314617003765
work_keys_str_mv AT devakumarmanikandan 34chlorobutyl3hindole5carbonitrile
AT sundaramoorthygomathi 34chlorobutyl3hindole5carbonitrile
AT jeyaramanselvarajnirmalram 34chlorobutyl3hindole5carbonitrile
AT sadasivamsharmilatagore 34chlorobutyl3hindole5carbonitrile
AT velusamysethuraman 34chlorobutyl3hindole5carbonitrile
AT josephagim 34chlorobutyl3hindole5carbonitrile
AT raybutcher 34chlorobutyl3hindole5carbonitrile
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