2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors

Detalhes bibliográficos
Autor(a) principal: Nogueira, Bernardo A.
Data de Publicação: 2021
Outros Autores: 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
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/107464
https://doi.org/10.1021/acs.cgd.1c01123
Resumo: 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.
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spelling 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors2,4,6-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.ACS American Chemical Society2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/107464http://hdl.handle.net/10316/107464https://doi.org/10.1021/acs.cgd.1c01123eng1528-74831528-7505Nogueira, Bernardo A.Lopes, Susana M. M.Lopes, SusyNikitin, TimurRodrigues, Ana Clara B.Eusébio, Maria Ermelinda S.Paixão, J. A.Pinho e Melo, Teresa M. V. D.Milani, AlbertoCastiglioni, ChiaraFausto, Ruiinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-18T08:16:06Zoai:estudogeral.uc.pt:10316/107464Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:23:48.958985Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
title 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
spellingShingle 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
Nogueira, Bernardo A.
title_short 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
title_full 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
title_fullStr 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
title_full_unstemmed 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
title_sort 2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
author Nogueira, Bernardo A.
author_facet 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
author_role author
author2 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
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv 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
description 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.
publishDate 2021
dc.date.none.fl_str_mv 2021
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/107464
http://hdl.handle.net/10316/107464
https://doi.org/10.1021/acs.cgd.1c01123
url http://hdl.handle.net/10316/107464
https://doi.org/10.1021/acs.cgd.1c01123
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dc.publisher.none.fl_str_mv ACS American Chemical Society
publisher.none.fl_str_mv ACS American Chemical Society
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