Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107464
Title: 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
Authors: Nogueira, Bernardo A. 
Lopes, Susana M. M. 
Lopes, Susy 
Nikitin, Timur 
Rodrigues, Ana Clara B. 
Eusébio, Maria Ermelinda S. 
Paixão, J. A. 
Pinho e Melo, Teresa M. V. D. 
Milani, Alberto 
Castiglioni, Chiara 
Fausto, Rui 
Issue Date: 2021
Publisher: ACS American Chemical Society
Project: The CQC-IMS is financially supported by the Portuguese Science Foundation (“Fundação para a Ciência e a Tecnologia” - FCT) − Projects CQC UIDB/00313/2020 and UIDP/00313/2020 (National Funds). CFisUC is funded by FCT through the Projects UIDB/04564/2020 and UIDP/ 04564/2020. Access to instruments from Laser-Lab Coimbra and TAIL-UC (ICT_2009_02_012_1890) facilities funded under QREN-Mais Centro is gratefully acknowledged. B.A.N. also acknowledges FCT for the SFRH/BD/129852/2017 Ph.D. Scholarship. 
Serial title, monograph or event: Crystal Growth & Design
Volume: 21
Issue: 12
Abstract: 2,4,6-Trinitro-N-(m-tolyl)aniline or N-picryl-m-toluidine (abbreviated as TMA), exhibiting color polymorphism, was synthesized and characterized structurally, spectroscopically, and thermodynamically. The studies consider both the isolated molecule of the compound (studied theoretically at the DFT- (B3LYP)/6-311++G(d,p) level and experimentally by matrixisolation infrared spectroscopy) and its polymorphic crystalline phases. The investigations on the isolated molecule allowed us to evaluate the major intramolecular interactions determining the conformational preferences of the compound and characterize it in detail from the vibrational point of view. Two conformers were found (A and B), which differ in the relative orientation of the ring moieties of the molecule. Polymorph screening, by recrystallization of the compound using different solvents, allowed us to identify three different polymorphs, exhibiting red, orange, and yellow colors, which were subsequently characterized structurally by singlecrystal X-ray diffraction, vibrationally, by infrared and Raman spectroscopies (complemented by fully periodic differential functional theory calculations on the crystals), electronically, using solid-state ultraviolet−visible absorption spectroscopy, and thermodynamically, by differential scanning calorimetry and polarized light thermo-microscopy. The yellow polymorph was found to be a conformational polymorph of the orange and red ones, while the last two are packing polymorphs. Mechanistic insights into the causes of the different colors of the polymorphs are presented. On the whole, the reported investigation constitutes a comprehensive structural (for both the isolated molecule and crystalline phases), spectroscopic, and thermal analysis of the newly prepared compound, with particular emphasis on the rare color polymorphism it exhibits.
URI: https://hdl.handle.net/10316/107464
ISSN: 1528-7483
1528-7505
DOI: 10.1021/acs.cgd.1c01123
Rights: embargoedAccess
Appears in Collections:I&D CFis - Artigos em Revistas Internacionais
I&D CQC - Artigos em Revistas Internacionais

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