Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3

Detalhes bibliográficos
Ano de defesa: 2011
Autor(a) principal: Gois, Elba Pereira De lattes
Orientador(a): Almeida, Eduardo Tonon De lattes
Banca de defesa: Godoy Netto, Adelino Vieira De, Pissetti, Fábio Luiz
Tipo de documento: Dissertação
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/123456789/379
Resumo: In recent years there has been a significant increase in the number of research papers that report the use of transition metal compounds for therapeutic purposes. Many studies were based on the possible interactions of metal ions with bimolecular present in living organisms. It is known that the geometry of square-planar metal ions present in the palladium(II), platinum(II), gold(III), nickel(II) - strong field and iridium(I) - strong field, favors the ion-DNA interaction and drugs act mainly as intercalation inter-or intra-tape. This work was guided by the synthesis and characterization of new complexes of palladium(II) with potential pharmacological applications. We obtained a compound cyclometallated Pd(II) by reacting the ligand nitrogen cyclometallated H2ani2p-fen with tetracloropalad(II) of lithium in molar ratio (1:1 or 1:2). The complex stoichiometry (1:1) [Pd2(Hani2p-fen)2Cl2] C2 was used as precursor in the synthesis of five complexes, of halide substitution by chlorine and bromine and iodine pseudohalide azide, cyanate and thiocyanate: [Pd(H2L)X2], [Pd2(HL)2X2], [Pd4(H2L)2X4] and [Pd4L2X4] where X = N3, NCO, SCN, Br and I. Since the complex stoichiometry (1:2) [Pd4(Hani2p-fen)2(ani2p-fen)Cl4] C8 was used as precursor in the synthesis of more complex five others. Substitutions were also chlorine by halides (Br, I) and pseudohalide (N3, SCN and NCO), yielding the complexes: [Pd4(HL)2(L)X4] and [Pd4(L)2X4] where X = N3, NCO, SCN, Br and I. In addition to the spectroscopic techniques (UV-Vis, IR e NMR of 1H), Tests of solubility, melting point, elemental analysis (CHNS) and thermogravimetric studies (TG-DTA) for both the imine ligand, as for the complexes metal. Regarding the vibrational spectroscopy in the ultraviolet - visible, there was the shift of the absorption bands of the complexes indicating coordination of the ligand and the substitution of groups coordinated regiospecífies bridge. The technique of vibrational spectroscopy in the infrared region allowed inferring the mode of coordination of pseudohalide and confirms the presence of the ligand coordinated to the metal center. This technique confirmed that the azide, cyanate and thiocyanate groups are preferably coordinated so end-on, end-to-end and terminal. The analysis of NMR 1H spectra of ligand and complexes cyclopalladated nitrogen showed the presence of signs consistent with the proposed structures. Regarding the thermograms was possible to propose a mechanism for new thermodecomposition complex, because as the only waste met Pd identified by X-ray diffraction by the powder method. Aiming to employ these compounds in biological assays front of Leishmania, experiments were performed in vitro cell promastigotes and amastigotes of L. (L.) braziliensis. Determined the viability of these cultures, expressed by the Index of Cytotoxicity (IC50), which indicates the concentration of substance that induces death 50% of the cell population. The compounds that showed better leishmanicidal activity were those containing chlorine (C8) and thiocyanate (C11).
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spelling Gois, Elba Pereira Dehttp://lattes.cnpq.br/7388999275444692Torres, CláudiaGodoy Netto, Adelino Vieira DePissetti, Fábio LuizAlmeida, Eduardo Tonon Dehttp://lattes.cnpq.br/73889992754446922015-06-12T23:27:18Z2011-01-25GOIS, Elba Pereira de. Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3. 2011.155 f. Dissertação (Mestrado em Química) - Universidade Federal de Alfenas, Alfenas, MG, 2011.https://repositorio.unifal-mg.edu.br/handle/123456789/379In recent years there has been a significant increase in the number of research papers that report the use of transition metal compounds for therapeutic purposes. Many studies were based on the possible interactions of metal ions with bimolecular present in living organisms. It is known that the geometry of square-planar metal ions present in the palladium(II), platinum(II), gold(III), nickel(II) - strong field and iridium(I) - strong field, favors the ion-DNA interaction and drugs act mainly as intercalation inter-or intra-tape. This work was guided by the synthesis and characterization of new complexes of palladium(II) with potential pharmacological applications. We obtained a compound cyclometallated Pd(II) by reacting the ligand nitrogen cyclometallated H2ani2p-fen with tetracloropalad(II) of lithium in molar ratio (1:1 or 1:2). The complex stoichiometry (1:1) [Pd2(Hani2p-fen)2Cl2] C2 was used as precursor in the synthesis of five complexes, of halide substitution by chlorine and bromine and iodine pseudohalide azide, cyanate and thiocyanate: [Pd(H2L)X2], [Pd2(HL)2X2], [Pd4(H2L)2X4] and [Pd4L2X4] where X = N3, NCO, SCN, Br and I. Since the complex stoichiometry (1:2) [Pd4(Hani2p-fen)2(ani2p-fen)Cl4] C8 was used as precursor in the synthesis of more complex five others. Substitutions were also chlorine by halides (Br, I) and pseudohalide (N3, SCN and NCO), yielding the complexes: [Pd4(HL)2(L)X4] and [Pd4(L)2X4] where X = N3, NCO, SCN, Br and I. In addition to the spectroscopic techniques (UV-Vis, IR e NMR of 1H), Tests of solubility, melting point, elemental analysis (CHNS) and thermogravimetric studies (TG-DTA) for both the imine ligand, as for the complexes metal. Regarding the vibrational spectroscopy in the ultraviolet - visible, there was the shift of the absorption bands of the complexes indicating coordination of the ligand and the substitution of groups coordinated regiospecífies bridge. The technique of vibrational spectroscopy in the infrared region allowed inferring the mode of coordination of pseudohalide and confirms the presence of the ligand coordinated to the metal center. This technique confirmed that the azide, cyanate and thiocyanate groups are preferably coordinated so end-on, end-to-end and terminal. The analysis of NMR 1H spectra of ligand and complexes cyclopalladated nitrogen showed the presence of signs consistent with the proposed structures. Regarding the thermograms was possible to propose a mechanism for new thermodecomposition complex, because as the only waste met Pd identified by X-ray diffraction by the powder method. Aiming to employ these compounds in biological assays front of Leishmania, experiments were performed in vitro cell promastigotes and amastigotes of L. (L.) braziliensis. Determined the viability of these cultures, expressed by the Index of Cytotoxicity (IC50), which indicates the concentration of substance that induces death 50% of the cell population. The compounds that showed better leishmanicidal activity were those containing chlorine (C8) and thiocyanate (C11).Nos últimos anos verificou-se um aumento significativo no número de trabalhos de pesquisa que relatam a utilização de compostos de metais de transição com fins terapêuticos. Muitos estudos tomaram como base as possíveis interações dos íons metálicos com as biomoléculas presentes no organismo vivo. Sabe-se que a geometria quadrado-planar presentes nos íons metálicos paládio(II), platina(II), ouro(III), níquel(II) - campo forte e irídio(I) - campo forte, favorece a interação íon-DNA e atuam principalmente como drogas intercaladoras de modo inter ou intra-fita. O presente trabalho foi norteado pela síntese e caracterização de novos complexos de paládio(II) com possíveis aplicações farmacológicas. Foi obtido um composto ciclometalado de Pd(II) mediante reação de ciclometalação do ligante nitrogenado H2ani2p-fen com tetracloropaladato(II) de lítio, nas proporções estequiométricas (1:1 e 1:2). O complexo da estequiometria (1:1) [Pd2(Hani2p-fen)2Cl2] C2 foi utilizado como precursor na síntese de outros cincos complexos, por substituição do cloro por haletos bromo e iodo e pseudohaletos azida, cianato e tiocianato: [Pd(H2L)X2], [Pd2(HL)2X2], [Pd4(H2L)2X4] e [Pd4L2X4] sendo X = N3, NCO, SCN, Br e I. Já o complexo da estequiometria (1:2) [Pd4(Hani2p-fen)2(ani2p-fen)Cl4] C8 foi utilizado como precursor na síntese de mais outros cincos complexos. As substituições também foram do cloro por haletos (Br, I) e pseudohaletos (N3, NCO e SCN), obtendo os complexos: [Pd4(HL)2(L)X4] e [Pd4(L)2X4] sendo X = N3, NCO, SCN, Br e I. Além das técnicas espectroscópicas (IV, UV-Vis, RMN de 1H), foram realizados testes de solubilidade, ponto de fusão, análise elementar (CHNS) e estudos termogravimétricos (TG-DTA), tanto para o ligante imínico, como para os complexos metálicos. No tocante, a espectroscopia vibracional na região do ultravioleta – visível, foi observado o deslocamento das bandas de absorção dos complexos indicando a coordenação do ligante, bem como a substituição regioespecífica dos grupos coordenados em ponte. A técnica de espectroscopia vibracional na região do infravermelho permitiu inferir sobre o modo de coordenação dos pseudohaletos e confirmar a presença do ligante coordenado ao centro metálico. Esta técnica confirmou que os grupos azida, cianato e tiocianato estão coordenados preferencialmente de modo end-on, end-to-end e terminal. A análise dos espectros de RMN de 1H ligante nitrogenado e dos complexos ciclopaladados mostrou a presença de sinais compatíveis com as estruturas propostas. Em relação às curvas termogravimétricas foi possível propor um mecanismo de termodecomposição para os novos complexos, pois como único resíduo encontrou-se paládio metálico, identificado por difração de raios-X pelo método de pó. Visando empregar estes compostos em ensaios biológicos frente à Leishmania, foram realizados experimentos in vitro de células promastigotas e amastigotas da L. (L.) brazilienses. Determinou-se a viabilidade celular destas culturas, expressa pelo Índice de Citotoxicidade (IC50), que indica a concentração de substância que induz à morte 50% da população celular. Os complexos que apresentaram melhor atividade leishmanicida foram os derivados que contêm cloro (C8) e tiocianato (C11).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/Paládio - SínteseSchiff, Bases deLeishmaniaQUIMICA::QUIMICA INORGANICAAspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3info:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/publishedVersion13282530788267823066006003139127065238931096reponame:Repositório Institucional da Universidade Federal de Alfenas - RiUnifalinstname:Universidade Federal de Alfenas (UNIFAL)instacron:UNIFALGois, Elba Pereira DeLICENSElicense.txtlicense.txttext/plain; charset=utf-81987https://repositorio.unifal-mg.edu.br/bitstreams/1de375c2-0b6d-443a-8585-495889d6e05a/download31555718c4fc75849dd08f27935d4f6bMD51CC-LICENSElicense_urllicense_urltext/plain; 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dc.title.pt-BR.fl_str_mv Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
title Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
spellingShingle Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
Gois, Elba Pereira De
Paládio - Síntese
Schiff, Bases de
Leishmania
QUIMICA::QUIMICA INORGANICA
title_short Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
title_full Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
title_fullStr Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
title_full_unstemmed Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
title_sort Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3
author Gois, Elba Pereira De
author_facet Gois, Elba Pereira De
author_role author
dc.contributor.author.fl_str_mv Gois, Elba Pereira De
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/7388999275444692
dc.contributor.advisor-co1.fl_str_mv Torres, Cláudia
dc.contributor.referee1.fl_str_mv Godoy Netto, Adelino Vieira De
dc.contributor.referee2.fl_str_mv Pissetti, Fábio Luiz
dc.contributor.advisor1.fl_str_mv Almeida, Eduardo Tonon De
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/7388999275444692
contributor_str_mv Torres, Cláudia
Godoy Netto, Adelino Vieira De
Pissetti, Fábio Luiz
Almeida, Eduardo Tonon De
dc.subject.por.fl_str_mv Paládio - Síntese
Schiff, Bases de
Leishmania
topic Paládio - Síntese
Schiff, Bases de
Leishmania
QUIMICA::QUIMICA INORGANICA
dc.subject.cnpq.fl_str_mv QUIMICA::QUIMICA INORGANICA
description In recent years there has been a significant increase in the number of research papers that report the use of transition metal compounds for therapeutic purposes. Many studies were based on the possible interactions of metal ions with bimolecular present in living organisms. It is known that the geometry of square-planar metal ions present in the palladium(II), platinum(II), gold(III), nickel(II) - strong field and iridium(I) - strong field, favors the ion-DNA interaction and drugs act mainly as intercalation inter-or intra-tape. This work was guided by the synthesis and characterization of new complexes of palladium(II) with potential pharmacological applications. We obtained a compound cyclometallated Pd(II) by reacting the ligand nitrogen cyclometallated H2ani2p-fen with tetracloropalad(II) of lithium in molar ratio (1:1 or 1:2). The complex stoichiometry (1:1) [Pd2(Hani2p-fen)2Cl2] C2 was used as precursor in the synthesis of five complexes, of halide substitution by chlorine and bromine and iodine pseudohalide azide, cyanate and thiocyanate: [Pd(H2L)X2], [Pd2(HL)2X2], [Pd4(H2L)2X4] and [Pd4L2X4] where X = N3, NCO, SCN, Br and I. Since the complex stoichiometry (1:2) [Pd4(Hani2p-fen)2(ani2p-fen)Cl4] C8 was used as precursor in the synthesis of more complex five others. Substitutions were also chlorine by halides (Br, I) and pseudohalide (N3, SCN and NCO), yielding the complexes: [Pd4(HL)2(L)X4] and [Pd4(L)2X4] where X = N3, NCO, SCN, Br and I. In addition to the spectroscopic techniques (UV-Vis, IR e NMR of 1H), Tests of solubility, melting point, elemental analysis (CHNS) and thermogravimetric studies (TG-DTA) for both the imine ligand, as for the complexes metal. Regarding the vibrational spectroscopy in the ultraviolet - visible, there was the shift of the absorption bands of the complexes indicating coordination of the ligand and the substitution of groups coordinated regiospecífies bridge. The technique of vibrational spectroscopy in the infrared region allowed inferring the mode of coordination of pseudohalide and confirms the presence of the ligand coordinated to the metal center. This technique confirmed that the azide, cyanate and thiocyanate groups are preferably coordinated so end-on, end-to-end and terminal. The analysis of NMR 1H spectra of ligand and complexes cyclopalladated nitrogen showed the presence of signs consistent with the proposed structures. Regarding the thermograms was possible to propose a mechanism for new thermodecomposition complex, because as the only waste met Pd identified by X-ray diffraction by the powder method. Aiming to employ these compounds in biological assays front of Leishmania, experiments were performed in vitro cell promastigotes and amastigotes of L. (L.) braziliensis. Determined the viability of these cultures, expressed by the Index of Cytotoxicity (IC50), which indicates the concentration of substance that induces death 50% of the cell population. The compounds that showed better leishmanicidal activity were those containing chlorine (C8) and thiocyanate (C11).
publishDate 2011
dc.date.issued.fl_str_mv 2011-01-25
dc.date.accessioned.fl_str_mv 2015-06-12T23:27:18Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.identifier.citation.fl_str_mv GOIS, Elba Pereira de. Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3. 2011.155 f. Dissertação (Mestrado em Química) - Universidade Federal de Alfenas, Alfenas, MG, 2011.
dc.identifier.uri.fl_str_mv https://repositorio.unifal-mg.edu.br/handle/123456789/379
identifier_str_mv GOIS, Elba Pereira de. Aspectos estruturais e potencialidade leishmanicida de compostos de paládio(II) ciclometalados ou não, com o ligante imínico H3C-O-p-C6H4-(E)HC=N-C6H4-p-N=CH(E)-C6H4-p-O-CH3. 2011.155 f. Dissertação (Mestrado em Química) - Universidade Federal de Alfenas, Alfenas, MG, 2011.
url https://repositorio.unifal-mg.edu.br/handle/123456789/379
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language por
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dc.relation.confidence.fl_str_mv 600
600
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dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Universidade Federal de Alfenas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química
dc.publisher.initials.fl_str_mv UNIFAL-MG
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Instituto de Química
publisher.none.fl_str_mv Universidade Federal de Alfenas
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