Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica.
| Ano de defesa: | 2020 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | , , , |
| Tipo de documento: | Tese |
| Tipo de acesso: | Acesso aberto |
| Idioma: | por |
| Instituição de defesa: |
Universidade Federal de Alfenas
|
| Programa de Pós-Graduação: |
Programa de Pós-Graduação em Química
|
| Departamento: |
Instituto de Química
|
| País: |
Brasil
|
| Palavras-chave em Português: | |
| Área do conhecimento CNPq: | |
| Link de acesso: | https://repositorio.unifal-mg.edu.br/handle/123456789/1836 |
Resumo: | This work presents the synthesis of new palladium (II) compounds from three Schiff bases, N,N-metfen-sOH (L 1 ), N,N-etfen-sOH (L 2 ) and N,N-etdiben (L 3 ). The reaction of these ligands with the palladium precursors, [Pd(AcO) 2 ] e Li 2 [PdCl 4 ] formed three new compounds: [Pd(N,N-metfen-sO) 2 ] (C 1 ), [Pd(N,N-etfen-sO) 2 ] (C 2 ) and [Pd(- AcO)( N,N-etdiben)] 2 (C 3 a). The substitution of complex C 3 a acetates by chlorides, bromides, azides and thiocyanates, and the reaction of this same complex with triphenylphosphine formed others five new complexes. All synthesized compounds, including Schiff bases, were previously characterized by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), CHN elemental analysis, simultaneous thermogravimetry and differential thermal analysis (TGA-DTA) and single crystal X- ray diffraction. Single crystals of compounds C 1 and C 2 were obtained, and the resolution of these structures was very important for the structural elucidation of these compounds. From the X-ray data, the Hirshfeld surfaces were also obtained, complementing the supramolecular characterization of these complexes. The infrared and NMR spectra agree with the proposed structures, indicating the coordination mode of singular synthesized complex. Elemental analysis agrees with the proposed structures. The residual mass of the thermogravimetry analysis agree with the proposed palladium content on structures. The thermal analysis was also used to compare the thermal stability of compounds after substitution reactions. DFT calculations were important for understanding some properties of these complexes, in addition to corroborating the proposed coordination modes. Preliminary experiments to determine the cytotoxic potential of the compounds were carried out against MCF-7 (human breast adenocarcinoma), HepG2 (human liver adenocarcinoma) and A549 (human lung epithelial adenocarcinoma) and showed that three of the new synthesized compounds cause a small decrease in cell viability of this tumor cell line, mainly MCF-7. |
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Sarto, Luís Eduardohttp://lattes.cnpq.br/6402668883583711Torres, ClaudiaNascimento, André Luiz Carneiro Soares DoPisseti, Fábio LuizD’Assunção, Lázaro MoscardiniVillis, Paulo César MendesAlmeida, Eduardo Tonon Dehttp://lattes.cnpq.br/78033014459933142021-06-25T17:53:19Z2020-02-19SARTO, Luís Eduardo. Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica.. 2020. 137 f. Tese (Doutorado em Química) - Universidade Federal de Alfenas, Alfenas/MG, 2020.https://repositorio.unifal-mg.edu.br/handle/123456789/1836This work presents the synthesis of new palladium (II) compounds from three Schiff bases, N,N-metfen-sOH (L 1 ), N,N-etfen-sOH (L 2 ) and N,N-etdiben (L 3 ). The reaction of these ligands with the palladium precursors, [Pd(AcO) 2 ] e Li 2 [PdCl 4 ] formed three new compounds: [Pd(N,N-metfen-sO) 2 ] (C 1 ), [Pd(N,N-etfen-sO) 2 ] (C 2 ) and [Pd(- AcO)( N,N-etdiben)] 2 (C 3 a). The substitution of complex C 3 a acetates by chlorides, bromides, azides and thiocyanates, and the reaction of this same complex with triphenylphosphine formed others five new complexes. All synthesized compounds, including Schiff bases, were previously characterized by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), CHN elemental analysis, simultaneous thermogravimetry and differential thermal analysis (TGA-DTA) and single crystal X- ray diffraction. Single crystals of compounds C 1 and C 2 were obtained, and the resolution of these structures was very important for the structural elucidation of these compounds. From the X-ray data, the Hirshfeld surfaces were also obtained, complementing the supramolecular characterization of these complexes. The infrared and NMR spectra agree with the proposed structures, indicating the coordination mode of singular synthesized complex. Elemental analysis agrees with the proposed structures. The residual mass of the thermogravimetry analysis agree with the proposed palladium content on structures. The thermal analysis was also used to compare the thermal stability of compounds after substitution reactions. DFT calculations were important for understanding some properties of these complexes, in addition to corroborating the proposed coordination modes. Preliminary experiments to determine the cytotoxic potential of the compounds were carried out against MCF-7 (human breast adenocarcinoma), HepG2 (human liver adenocarcinoma) and A549 (human lung epithelial adenocarcinoma) and showed that three of the new synthesized compounds cause a small decrease in cell viability of this tumor cell line, mainly MCF-7.O presente trabalho envolve a preparação de novos compostos de paládio(II), a partir de três bases de Schiff, N,N-metfen-sOH (L 1 ), N,N-etfen-sOH (L 2 ) e N,N- etdiben (L 3 ) A partir da reação desses ligantes com os precursores de paládio, [Pd(AcO) 2 ] e Li 2 [PdCl 4 ], foram sintetizados três novos complexos: [Pd(N,N-metfen- sO) 2 ] (C 1 ), [Pd(N,N-etfen-sO) 2 ] (C 2 ) e [Pd(-AcO)( N,N-etdiben)] 2 (C 3 a). A substituição dos acetatos do complexo C 3 a por cloretos, brometos, azidas e tiocianatos, e a reação desse mesmo complexo com trifenilfosfina, originou mais cinco complexos. Todos os compostos sintetizados, inclusive as bases de Schiff, foram previamente caracterizados por espectroscopia de absorção na região do infravermelho (IV) e de ressonância magnética nuclear (RMN), análise elementar CHN, termogravimetria e análise térmica diferencial simultâneas (TGA-DTA) e difração de raios X de monocristal (DRX). Foram obtidos monocristais dos compostos C 1 e C 2 , e a resolução dessas estruturas foi de suma importância para a elucidação estrutural desses compostos. A partir dos dados de raios X, também foram obtidas as superfícies de Hirshfeld, sendo essa uma ferramenta muito importante na discussão da Química Supramolecular desses complexos. Os espectros obtidos no infravermelho e no RMN corroboram as propostas estruturais, indicando o modo de coordenação de ca da um dos complexos sintetizados. Resultados de análise elementar CHN concordam com as estruturas propostas. As curvas termogravimétricas apresentaram massas residuais condizentes com o teor de paládio proposto para cada um dos complexos, além de elucidar diferenças de estabilidade térmica causadas pelas reações de substituição. Os cálculos de DFT foram importantes para a compreensão de algumas propriedades desses complexos, além de corroborarem os modos de coordenação propostos. Experimentos preliminares para determinar o potencial citotóxico dos compostos foram realizados frente a MCF-7 (adenocarcinoma mamário humano), HepG2 (adenocarcinoma hepático humano) e A549 (adenocarcinoma epitelial de pulmão humano) e mostraram que três dos novos compostos sintetizados causaram uma pequena diminuição na viabilidade celular dessas linhagens de células tumorais, principalmente da MCF-7.application/pdfporUniversidade Federal de AlfenasPrograma de Pós-Graduação em QuímicaUNIFAL-MGBrasilInstituto de Químicainfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/Complexos de Paládio(II)Base de SchiffDifração de raios XSuperfície de HirshfeldDFTQUIMICA::QUIMICA INORGANICAComplexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica.info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion13282530788267823066006003139127065238931096reponame:Biblioteca Digital de Teses e Dissertações da UNIFALinstname:Universidade Federal de Alfenas (UNIFAL)instacron:UNIFALSarto, Luís EduardoCC-LICENSElicense_urllicense_urltext/plain; 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| dc.title.pt-BR.fl_str_mv |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. |
| title |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. |
| spellingShingle |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. Sarto, Luís Eduardo Complexos de Paládio(II) Base de Schiff Difração de raios X Superfície de Hirshfeld DFT QUIMICA::QUIMICA INORGANICA |
| title_short |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. |
| title_full |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. |
| title_fullStr |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. |
| title_full_unstemmed |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. |
| title_sort |
Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica. |
| author |
Sarto, Luís Eduardo |
| author_facet |
Sarto, Luís Eduardo |
| author_role |
author |
| dc.contributor.author.fl_str_mv |
Sarto, Luís Eduardo |
| dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/6402668883583711 |
| dc.contributor.advisor-co1.fl_str_mv |
Torres, Claudia |
| dc.contributor.referee1.fl_str_mv |
Nascimento, André Luiz Carneiro Soares Do |
| dc.contributor.referee2.fl_str_mv |
Pisseti, Fábio Luiz |
| dc.contributor.referee3.fl_str_mv |
D’Assunção, Lázaro Moscardini |
| dc.contributor.referee4.fl_str_mv |
Villis, Paulo César Mendes |
| dc.contributor.advisor1.fl_str_mv |
Almeida, Eduardo Tonon De |
| dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/7803301445993314 |
| contributor_str_mv |
Torres, Claudia Nascimento, André Luiz Carneiro Soares Do Pisseti, Fábio Luiz D’Assunção, Lázaro Moscardini Villis, Paulo César Mendes Almeida, Eduardo Tonon De |
| dc.subject.por.fl_str_mv |
Complexos de Paládio(II) Base de Schiff Difração de raios X Superfície de Hirshfeld DFT |
| topic |
Complexos de Paládio(II) Base de Schiff Difração de raios X Superfície de Hirshfeld DFT QUIMICA::QUIMICA INORGANICA |
| dc.subject.cnpq.fl_str_mv |
QUIMICA::QUIMICA INORGANICA |
| description |
This work presents the synthesis of new palladium (II) compounds from three Schiff bases, N,N-metfen-sOH (L 1 ), N,N-etfen-sOH (L 2 ) and N,N-etdiben (L 3 ). The reaction of these ligands with the palladium precursors, [Pd(AcO) 2 ] e Li 2 [PdCl 4 ] formed three new compounds: [Pd(N,N-metfen-sO) 2 ] (C 1 ), [Pd(N,N-etfen-sO) 2 ] (C 2 ) and [Pd(- AcO)( N,N-etdiben)] 2 (C 3 a). The substitution of complex C 3 a acetates by chlorides, bromides, azides and thiocyanates, and the reaction of this same complex with triphenylphosphine formed others five new complexes. All synthesized compounds, including Schiff bases, were previously characterized by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), CHN elemental analysis, simultaneous thermogravimetry and differential thermal analysis (TGA-DTA) and single crystal X- ray diffraction. Single crystals of compounds C 1 and C 2 were obtained, and the resolution of these structures was very important for the structural elucidation of these compounds. From the X-ray data, the Hirshfeld surfaces were also obtained, complementing the supramolecular characterization of these complexes. The infrared and NMR spectra agree with the proposed structures, indicating the coordination mode of singular synthesized complex. Elemental analysis agrees with the proposed structures. The residual mass of the thermogravimetry analysis agree with the proposed palladium content on structures. The thermal analysis was also used to compare the thermal stability of compounds after substitution reactions. DFT calculations were important for understanding some properties of these complexes, in addition to corroborating the proposed coordination modes. Preliminary experiments to determine the cytotoxic potential of the compounds were carried out against MCF-7 (human breast adenocarcinoma), HepG2 (human liver adenocarcinoma) and A549 (human lung epithelial adenocarcinoma) and showed that three of the new synthesized compounds cause a small decrease in cell viability of this tumor cell line, mainly MCF-7. |
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2020 |
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2020-02-19 |
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2021-06-25T17:53:19Z |
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info:eu-repo/semantics/doctoralThesis |
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info:eu-repo/semantics/publishedVersion |
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SARTO, Luís Eduardo. Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica.. 2020. 137 f. Tese (Doutorado em Química) - Universidade Federal de Alfenas, Alfenas/MG, 2020. |
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https://repositorio.unifal-mg.edu.br/handle/123456789/1836 |
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SARTO, Luís Eduardo. Complexo de paládio com iminas derivadas de diaminas aromáticas: síntese, investigação estrutural, estudo térmico e atividade antineoplásica.. 2020. 137 f. Tese (Doutorado em Química) - Universidade Federal de Alfenas, Alfenas/MG, 2020. |
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https://repositorio.unifal-mg.edu.br/handle/123456789/1836 |
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por |
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600 600 |
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Instituto de Química |
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Universidade Federal de Alfenas |
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4afdbb8c545fd630ea7db775da747b2f d41d8cd98f00b204e9800998ecf8427e d41d8cd98f00b204e9800998ecf8427e 31555718c4fc75849dd08f27935d4f6b a1be7a058da9c212f478795e970dfcb6 28ab1625f1c17f816dd3b6223c3dbb72 f666eb9eaac83af7e60ef50cfea2cd67 |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 MD5 MD5 |
| repository.name.fl_str_mv |
Biblioteca Digital de Teses e Dissertações da UNIFAL - Universidade Federal de Alfenas (UNIFAL) |
| repository.mail.fl_str_mv |
bdtd@unifal-mg.edu.br || bdtd@unifal-mg.edu.br |
| _version_ |
1850508392922087424 |