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

Detalhes bibliográficos
Autor(a) principal: Nogueira, Bernardo Albuquerque
Data de Publicação: 2021
Outros Autores: 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
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.
id RCAP_ce5e2dfc090527b488997ae87cc7fdf5
oai_identifier_str oai:estudogeral.uc.pt:10316/99945
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling 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 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799134069662941184