2,4,6-Trinitro-N-(m-tolyl)aniline: A New Polymorphic Material Exhibiting Different Colors
Autor(a) principal: | |
---|---|
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/10316/107464 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. |
id |
RCAP_278322e911ea0fba58c96d1222d3d66b |
---|---|
oai_identifier_str |
oai:estudogeral.uc.pt:10316/107464 |
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)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 |
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/10316/107464 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 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1528-7483 1528-7505 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
ACS American Chemical Society |
publisher.none.fl_str_mv |
ACS 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_ |
1799134124455231488 |