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Synthesis and X-ray crystallography of N,N'-di(2-hydroxybenzylidene)hydrazine
Sohail Saeed (1,*)
, Naghmana Rashid (2) , Shaaban Kamel Mohamed (3) (1) Department of Chemistry, Research Complex, Allama Iqbal Open University, Islamabad-44000, Pakistan
(2) Department of Chemistry, Research Complex, Allama Iqbal Open University, Islamabad-44000, Pakistan
(3) Division of Chemistry and The Environmental Science, School of Science and The Environment, Manchester Metropolitan University, M15GD, England
(*) Corresponding Author
Received: 18 Dec 2016 | Revised: 07 Jan 2017 | Accepted: 08 Jan 2017 | Published: 31 Mar 2017 | Issue Date: March 2017
Abstract
The biologically active N,N'-di(2-hydroxybenzylidene)hydrazine has been synthesized and specifically characterized by X-ray crystallography. There are two molecules of N,N'-di(2-hydroxybenzylidene)hydrazine, C14H12N2O2, in the unit cell. The N,N'-di(2-hydroxy benzylidene)hydrazine molecule is planar, with maximum deviation from the mean plane being less than 0.028(2) Å. Intramolecular O-H···N hydrogen bonding interactions were observed in the crystal lattice which connected the molecules into chain running along b-axis.
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European Journal of Chemistry
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DOI: 10.5155/eurjchem.8.1.15-17.1521
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The National Engineering and Scientific Commission (NESCOM), Islamabad, Pakistan
Citations
[1]. Ikram Saadaoui, Fatma Krichen, Bochra Ben Salah, Riadh Ben Mansour, Nabil Miled, Ali Bougatef, Mohamed Kossentini
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Journal of Molecular Structure 1180, 344, 2019
DOI: 10.1016/j.molstruc.2018.12.008
[2]. Praveen Singh, Ranjeet Kumar, Ashish Kumar Tewari
Hydrogen bonding framework in imidazole derivatives: Crystal structure and Hirshfeld surface analysis
European Journal of Chemistry 11(1), 50, 2020
DOI: 10.5155/eurjchem.11.1.50-59.1945
[3]. Manish Kumar Dixit, Mrigendra Dubey
Li+-Induced fluorescent metallogel: a case of ESIPT-CHEF and ICT phenomenon
Physical Chemistry Chemical Physics 20(36), 23762, 2018
DOI: 10.1039/C8CP04579H
[4]. Nilankar Diyali, Meena Chettri, Abhranil De, Bhaskar Biswas
Synthesis, crystal structure, and antidiabetic property of hydrazine functionalized Schiff base: 1,2-Di(benzylidene)hydrazine
European Journal of Chemistry 13(2), 234, 2022
DOI: 10.5155/eurjchem.13.2.234-240.2265
References
[1]. Rajavel, P.; Senthil, M. S; Anitha, C. E-Journal Chem. 2008, 5(3), 620-626.
https://doi.org/10.1155/2008/583487
[2]. Ugras, H. I.; Basaran, I.; Kilic. T.; Cakir, U. J. Heterocyclic Chem. 2006, 43, 1679-1684.
https://doi.org/10.1002/jhet.5570430639
[3]. Wadher, S. J.; Puranik, M. P.; Karande, N. A.; Yeole, P. G. Int. J. Pharm. Tech. Res. 2009, 1, 22-33.
[4]. Elena, E. F.; Torres, L.; Antonia, M.; Mendialoey, M. A.; Sevela, M. T. Polyhedron 2000, 19, 441-451.
https://doi.org/10.1016/S0277-5387(99)00383-6
[5]. Mohamed, G. G.; Omar, M. M.; Hindy, A. M. Turk. J. Chem. 2006, 30, 361-382.
[6]. Siddiqui, H. L.; Iqbal, A.; Ahmad, S.; Weaver, G. W. Molecules 2006, 11, 206-211.
https://doi.org/10.3390/11020206
[7]. Oxford Diffraction, CrysAlis PRO and CrysAlis RED. Oxford Diffraction Ltd, Abingdon, Oxfordshire, England, 2010.
[8]. Sheldrick, G. M. Acta Cryst. A 2008, 64, 112-122.
https://doi.org/10.1107/S0108767307043930
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DOI Link: https://doi.org/10.5155/eurjchem.8.1.15-17.1521
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European Journal of Chemistry 2017, 8(1), 15-17 | doi: https://doi.org/10.5155/eurjchem.8.1.15-17.1521 | Get rights and content
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