Cocrystallization of Diphenylamine and Picric acid (1:2)-Reference-Cited by-同舟云学术

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Cocrystallization of Diphenylamine and Picric acid (1:2)

Published:2012 Issue:0 Volume:28 Page:31-32
ISSN:1883-3578
Container-title:X-ray Structure Analysis Online
language:en
Short-container-title:X-ray Structure Analysis Online

Author:

KAPOOR Kamini¹,GUPTA Vivek K.¹,VELMURUGAN R.²,SEKAR M.³

Affiliation:

1. X-ray Crystallography Laboratory, Post-Graduate Department of Physics & Electronics, University of Jammu

2. Department of Chemistry (Post Graduate and Research), Kongunadu Arts and Science College

3. Post Graduate and Research Department of Chemistry, Sri Ramakrishna Mission Vidyalaya College of Arts and Science

Publisher

Japan Society for Analytical Chemistry

Subject

Materials Chemistry,Analytical Chemistry

Link

https://www.jstage.jst.go.jp/article/xraystruct/28/0/28_0_31/_pdf

Reference9 articles.

1. Diphenylamine and derivatives in the environment: a review

2. 2. Y. In, H. Nagata, M. Doi, T. Ishida, and A. Wakahara, Acta Cryst., 1997, C53, 367.

3. 3. P. Zaderenko, M. S. Gil, P. Lo'pez, P. Ballesteros, I. Fonseca, and A. Albert, Acta Cryst., 1997, B53, 961.

4. 4. H. Nagata, Y. In, M. Doi, T. Ishida, and A. Wakahara, Acta Cryst., 1995, B51, 1051.

5. 5. G. Smith, U. D. Wermuth, and P. C. Healy, Acta Cryst., 2004, E60, o1800.

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1. 2,5-diphenyloxazole and 4-pyrrolidinopyridine as conformers to picric acid: Structural characterization coupled with Multivariate Statistical Analysis;Journal of Molecular Structure;2024-05

2. Cocrystallization of Paracetamol-Picric acid: Hirshfeld surface analysis, supramolecular architecture and third-order nonlinear optical properties;Journal of Molecular Structure;2019-08

3. Structural investigation and Hirshfeld surface analysis of three organic picrate salts;Zeitschrift für Kristallographie - Crystalline Materials;2017-07-19

4. Supramolecular architectures of N,N,N′,N′-tetrakis-(2-hydroxyethyl)ethylenediamine and tris(2-hydroxyethyl)amine with La(iii) picrate;RSC Adv.;2014-11-11

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