(Z)-N-(2-Iodophenyl)-4-nitrobenzimidoyl cyanide

Rodolfo Moreno-Fuquen; Andres C Garcia; Rodrigo Abonia; Luz M Jaramillo-Gomez; Alan R. Kennedy

doi:10.1107/S2414314616003151

(Z)-N-(2-Iodophenyl)-4-nitrobenzimidoyl cyanide

Rodolfo Moreno-Fuquen, Andres C Garcia, Rodrigo Abonia, Luz M Jaramillo-Gomez, Alan R. Kennedy

Pure And Applied Chemistry

Research output: Contribution to journal › Article › peer-review

34 Downloads (Pure)

Abstract

In the title molecule, C14H8IN3O2, the cyanide group is anti to the iodide
substituent of the adjacent benzene ring. The central segment is essentially
planar (r.m.s deviation = 0.0341 A ° ) and it is twisted away from the iodide- and
nitro-substituted benzene rings by 69.02 (9) and 15.83 (16), respectively. In the
crystal, molecules are linked by weak C—H N interactions, leading to C(8)
chains along [010].

Original language	English
Pages (from-to)	x160315
Number of pages	3
Journal	IUCr Data
Volume	1
Issue number	2
DOIs	https://doi.org/10.1107/S2414314616003151
Publication status	Published - 27 Feb 2016

Keywords

crystal structure
C—H⋯N interactions
α-iminonitrile

Access to Document

10.1107/S2414314616003151Licence: Unspecified

Moreno-Fuquen-etal-IUCRD2016-(Z)-N-(2-Iodophenyl)-4-nitrobenzimidoyl-cyanideFinal published version, 393 KBLicence: CC BY 4.0

x-ray diffractometer
Kennedy, A.
Pure And Applied Chemistry
Facility/equipment: Equipment

Cite this

@article{bd95f298f5b646c089fd2f1106490eec,

title = "(Z)-N-(2-Iodophenyl)-4-nitrobenzimidoyl cyanide",

abstract = "In the title molecule, C14H8IN3O2, the cyanide group is anti to the iodidesubstituent of the adjacent benzene ring. The central segment is essentiallyplanar (r.m.s deviation = 0.0341 A ° ) and it is twisted away from the iodide- andnitro-substituted benzene rings by 69.02 (9) and 15.83 (16), respectively. In thecrystal, molecules are linked by weak C—H N interactions, leading to C(8)chains along [010].",

keywords = "crystal structure, C—H⋯N interactions, α-iminonitrile",

author = "Rodolfo Moreno-Fuquen and Garcia, {Andres C} and Rodrigo Abonia and Jaramillo-Gomez, {Luz M} and Kennedy, {Alan R.}",

note = "Open access journal. As discussed previously for the sister journal Acta Cryst. Section E, the author proofs are in cif format that is currently unsupported by PURE. ",

year = "2016",

month = feb,

day = "27",

doi = "10.1107/S2414314616003151",

language = "English",

volume = "1",

pages = "x160315",

journal = "IUCr Data",

issn = "2414-3146",

number = "2",

}

TY - JOUR

T1 - (Z)-N-(2-Iodophenyl)-4-nitrobenzimidoyl cyanide

AU - Moreno-Fuquen, Rodolfo

AU - Garcia, Andres C

AU - Abonia, Rodrigo

AU - Jaramillo-Gomez, Luz M

AU - Kennedy, Alan R.

N1 - Open access journal. As discussed previously for the sister journal Acta Cryst. Section E, the author proofs are in cif format that is currently unsupported by PURE.

PY - 2016/2/27

Y1 - 2016/2/27

N2 - In the title molecule, C14H8IN3O2, the cyanide group is anti to the iodidesubstituent of the adjacent benzene ring. The central segment is essentiallyplanar (r.m.s deviation = 0.0341 A ° ) and it is twisted away from the iodide- andnitro-substituted benzene rings by 69.02 (9) and 15.83 (16), respectively. In thecrystal, molecules are linked by weak C—H N interactions, leading to C(8)chains along [010].

AB - In the title molecule, C14H8IN3O2, the cyanide group is anti to the iodidesubstituent of the adjacent benzene ring. The central segment is essentiallyplanar (r.m.s deviation = 0.0341 A ° ) and it is twisted away from the iodide- andnitro-substituted benzene rings by 69.02 (9) and 15.83 (16), respectively. In thecrystal, molecules are linked by weak C—H N interactions, leading to C(8)chains along [010].

KW - crystal structure

KW - C—H⋯N interactions

KW - α-iminonitrile

U2 - 10.1107/S2414314616003151

DO - 10.1107/S2414314616003151

M3 - Article

SN - 2414-3146

VL - 1

SP - x160315

JO - IUCr Data

JF - IUCr Data

IS - 2

ER -

(Z)-N-(2-Iodophenyl)-4-nitrobenzimidoyl cyanide

Abstract

Keywords

Access to Document

Fingerprint

Equipment

x-ray diffractometer

Cite this