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Synthesis and Single Crystal X‐Ray Structure of New (2E)‐2‐[3‐(1H‐Imidazol‐1‐yl)‐1‐phenylpropylidene]‐N‐phenylhydrazinecarboxamide
Author(s) -
Mohamed I. Attia,
Hazem A. Ghabbour,
Aida A. ElAzzouny,
Omar A. AlDeeb,
Maha S. Almutairi,
HoongKun Fun
Publication year - 2013
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.436
H-Index - 50
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2013/515309
Subject(s) - chemistry , intramolecular force , monoclinic crystal system , hydrogen bond , crystal structure , crystallography , intermolecular force , moiety , molecule , stereochemistry , imine , single crystal , catalysis , organic chemistry
Synthesis, spectroscopic characterization and X-ray crystal structure of a new (2E)-2-[3-(1H-imidazol-1-yl)-1-phenylpropylidene]-N-phenylhydrazinecarboxamide (4) are reported. The stereochemistry of the title compound 4, C19H19N5O, about the imine bond [1.296 (4) Å] was assigned to have (E)-configuration. In the urea moiety, the N–H entities are trans to each other, and one of these forms is an intramolecular N–H⋯H hydrogen bond. The compound crystallizes in the monoclinic space group P21/c with a = 5.8093 (2) Å, b = 20.5575 (6) Å, c = 14.0355 (5) Å, α = 90.00°, β = 97.365° (2), γ = 90.00°, V = 1662.36 (10) Å3, and Z = 4. The molecules are packed in crystal structure by weak intermolecular hydrogen interactions

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