2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/99945 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 matrix isolation infrared spectroscopy) and its polymorphic crystalline phases. The investigations on the isolated molecule allowed 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 to identify three different polymorphs, exhibiting red, orange and yellow colors, which were subsequently characterized structurally by single crystal X-ray diffraction, vibrationally, by infrared and Raman spectroscopies (complemented by fully-periodic DFT calculations on the crystals), electronically, using solid state ultraviolet-visible absorption spectroscopy, and thermodynamically, by differential scanning calorimetry and polarized light thermomicroscopy. 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 on 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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2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors2,4,6-trinitro-N-(m-tolyl)anilinecolor polymorphismmolecular structurecrystal structurethermal analysisinfrared, Raman and UV-Vis spectroscopies2,4,6-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 matrix isolation infrared spectroscopy) and its polymorphic crystalline phases. The investigations on the isolated molecule allowed 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 to identify three different polymorphs, exhibiting red, orange and yellow colors, which were subsequently characterized structurally by single crystal X-ray diffraction, vibrationally, by infrared and Raman spectroscopies (complemented by fully-periodic DFT calculations on the crystals), electronically, using solid state ultraviolet-visible absorption spectroscopy, and thermodynamically, by differential scanning calorimetry and polarized light thermomicroscopy. 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 on 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.American Chemical Society2021-11-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/99945http://hdl.handle.net/10316/99945https://doi.org/10.1021/acs.cgd.1c01123eng1528-7483Nogueira, Bernardo AlbuquerqueLopes, Susana Margarida MartinsLopes, Susy BrancoNikitin, TimurRodrigues, Ana Clara BeltranEusébio, Maria Ermelinda da SilvaPaixão, José António de CarvalhoMelo, Teresa Margarida Vasconcelos Dias de Pinho eMilani, 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:RCAAP2022-08-31T10:45:55Zoai:estudogeral.uc.pt:10316/99945Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:17:25.819454Repositório 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 Albuquerque 2,4,6-trinitro-N-(m-tolyl)aniline color polymorphism molecular structure crystal structure thermal analysis infrared, Raman and UV-Vis spectroscopies |
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 Albuquerque |
author_facet |
Nogueira, Bernardo Albuquerque Lopes, Susana Margarida Martins Lopes, Susy Branco Nikitin, Timur Rodrigues, Ana Clara Beltran Eusébio, Maria Ermelinda da Silva Paixão, José António de Carvalho Melo, Teresa Margarida Vasconcelos Dias de Pinho e Milani, Alberto Castiglioni, Chiara Fausto, Rui |
author_role |
author |
author2 |
Lopes, Susana Margarida Martins Lopes, Susy Branco Nikitin, Timur Rodrigues, Ana Clara Beltran Eusébio, Maria Ermelinda da Silva Paixão, José António de Carvalho Melo, Teresa Margarida Vasconcelos Dias de Pinho e 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 Albuquerque Lopes, Susana Margarida Martins Lopes, Susy Branco Nikitin, Timur Rodrigues, Ana Clara Beltran Eusébio, Maria Ermelinda da Silva Paixão, José António de Carvalho Melo, Teresa Margarida Vasconcelos Dias de Pinho e Milani, Alberto Castiglioni, Chiara Fausto, Rui |
dc.subject.por.fl_str_mv |
2,4,6-trinitro-N-(m-tolyl)aniline color polymorphism molecular structure crystal structure thermal analysis infrared, Raman and UV-Vis spectroscopies |
topic |
2,4,6-trinitro-N-(m-tolyl)aniline color polymorphism molecular structure crystal structure thermal analysis infrared, Raman and UV-Vis spectroscopies |
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 matrix isolation infrared spectroscopy) and its polymorphic crystalline phases. The investigations on the isolated molecule allowed 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 to identify three different polymorphs, exhibiting red, orange and yellow colors, which were subsequently characterized structurally by single crystal X-ray diffraction, vibrationally, by infrared and Raman spectroscopies (complemented by fully-periodic DFT calculations on the crystals), electronically, using solid state ultraviolet-visible absorption spectroscopy, and thermodynamically, by differential scanning calorimetry and polarized light thermomicroscopy. 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 on 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 |
2021-11-18 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10316/99945 http://hdl.handle.net/10316/99945 https://doi.org/10.1021/acs.cgd.1c01123 |
url |
http://hdl.handle.net/10316/99945 https://doi.org/10.1021/acs.cgd.1c01123 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1528-7483 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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