Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila

Detalhes bibliográficos
Ano de defesa: 2013
Autor(a) principal: Zambiazi, Priscilla Jussiane lattes
Orientador(a): Hörner, Manfredo lattes
Banca de defesa: Bresolin, Leandro lattes, Squizani, Fatima lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Química
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/10543
Resumo: This study shows the triazenes ligands and complexes Pd(II), K+ and Au(I) obtained from reactions of the ligands with fragments para-sulfonamidephenyl, comprising triazene ligand 1,3-bis (4 - sulfonamidephenyl) (1) and the complex {trans-Bis[1,3-bis(4-sulfonamidephenyl)triazenide-κN1]bis(pyridine-κN)palladium(II)}{tetra(pyridine-κN)palladium(II)}bis(potssium)·water (2) and for compounds containing orto-halophenyl fragments represented by [1,3-bis(2-fluorophenyl)triazenide-κN1](triphenylphosphine- κP)gold(I) (3), [1,3-bis(2-chlorinephenyl)triazenide-κN1](triphenylphosphine-κP)gold(I) (4), [1,3-bis(2-bromidephenyl)triazenide-κN1](triphenylphosphine-κP)gold(I) (5) and [1,3-bis(2-iodinephenyl)triazenide-κN1](triphenylphosphine - κP)gold(I) (6) complexes. The compounds reported were characterized by X-ray diffraction on single crystal, and their structures in solid state are formed through supramolecular arrangements via classical and non-classical hydrogen bonding, as in the case of the compounds with the sulfonamide grouping, one can observe the formation of supramolecular synthons. In complexes 4, 5 and 6 it is observed to occur interactions halogen···halogen characterized by the formation of dimeric units associated by a center of inversion, besides having geometries classified by the angle of the links formed between the halogen and carbon atoms. Compounds 1, 2, 3, 4, 5 and 6 were subjected to evaluation front of biological activity, such as plasmidial DNA cleavage studies, evaluation of cytotoxicity and antibacterial activity, showing promising results.
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spelling 2017-05-222017-05-222013-03-08ZAMBIAZI, Priscilla Jussiane. Synthesis, crystallographic analysis and biological activity of the complexes with triazenides ligands with orto-halophenyl and para-sulfonamidephenyl fragments. 2013. 168 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2013.http://repositorio.ufsm.br/handle/1/10543This study shows the triazenes ligands and complexes Pd(II), K+ and Au(I) obtained from reactions of the ligands with fragments para-sulfonamidephenyl, comprising triazene ligand 1,3-bis (4 - sulfonamidephenyl) (1) and the complex {trans-Bis[1,3-bis(4-sulfonamidephenyl)triazenide-κN1]bis(pyridine-κN)palladium(II)}{tetra(pyridine-κN)palladium(II)}bis(potssium)·water (2) and for compounds containing orto-halophenyl fragments represented by [1,3-bis(2-fluorophenyl)triazenide-κN1](triphenylphosphine- κP)gold(I) (3), [1,3-bis(2-chlorinephenyl)triazenide-κN1](triphenylphosphine-κP)gold(I) (4), [1,3-bis(2-bromidephenyl)triazenide-κN1](triphenylphosphine-κP)gold(I) (5) and [1,3-bis(2-iodinephenyl)triazenide-κN1](triphenylphosphine - κP)gold(I) (6) complexes. The compounds reported were characterized by X-ray diffraction on single crystal, and their structures in solid state are formed through supramolecular arrangements via classical and non-classical hydrogen bonding, as in the case of the compounds with the sulfonamide grouping, one can observe the formation of supramolecular synthons. In complexes 4, 5 and 6 it is observed to occur interactions halogen···halogen characterized by the formation of dimeric units associated by a center of inversion, besides having geometries classified by the angle of the links formed between the halogen and carbon atoms. Compounds 1, 2, 3, 4, 5 and 6 were subjected to evaluation front of biological activity, such as plasmidial DNA cleavage studies, evaluation of cytotoxicity and antibacterial activity, showing promising results.Este trabalho apresenta o estudo de ligantes triazenos e complexos de Pd(II), K+ e Au(I) obtidos a partir de reações com os ligantes com fragmentos para-sulfonamidafenila compreendendo o ligante 1,3-bis-(4-sulfonamidafenil)triazeno (1) e o complexo {trans-Bis[1,3-bis(4-sulfonamidafenil)triazenido-κN1]bis(piridina-κN)paládio(II)}{tetra(piridina-κN)paládio(II)}bis(potássio)·água (2) e para compostos contendo fragmentos orto-halofenila representados pelos complexos [1,3-bis(2-fluorofenil)triazenido-κN1](trifenilfosfina- κP)ouro(I) (3), [1,3-bis(2-clorofenil)triazenido-κN1](trifenilfosfina- κP)ouro(I) (4), [1,3-bis(2-bromofenil)triazenido-κN1](trifenilfosfina- κP)ouro(I) (5) e [1,3-bis(2-iodofenil)triazenido-κ-N1](trifenilfosfina- κP)ouro(I) (6). Os compostos relatados foram caracterizados por difração de raios X em monocristal, e suas estruturas no estado sólido são formadas através de arranjos supramoleculares via ligações de hidrogênio clássicas e não clássicas, como no caso dos compostos com o grupamento sulfonamida, pode-se observar a formação de synthons supramoleculares. Nos complexos 4, 5 e 6 é observada a ocorrência de interações halogênio···halogênio caracterizadas pela formação de unidades díméricas associadas por um centro de inversão, além de apresentarem geometrias classificadas pelo ângulo de ligações formado entre os átomos de halogênio e carbono. Os compostos 1, 2, 3, 4, 5 e 6 foram submetidos a avaliação frente a atividade biológica, como estudos na clivagem do DNA plasmidial, avaliação da citotoxicidade e atividade antibacteriana, mostrando resultados promissores.Conselho Nacional de Desenvolvimento Científico e Tecnológicoapplication/pdfporUniversidade Federal de Santa MariaPrograma de Pós-Graduação em QuímicaUFSMBRQuímicaTriazenosComplexos de Pd(II)K+ e Au(I)Synthons supramolecularesInterações halogênio···halogênioAtividade biológicaTriazenesComplexes of Pd(II)K+ and Au(I)Supramolecular synthonsHalogen···halogen interactionsBiological activityCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICASíntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenilaSynthesis, crystallographic analysis and biological activity of the complexes with triazenides ligands with orto-halophenyl and para-sulfonamidephenyl fragmentsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisHörner, Manfredohttp://lattes.cnpq.br/8922528250830998Bresolin, Leandrohttp://lattes.cnpq.br/3961672079507969Squizani, Fatimahttp://lattes.cnpq.br/1060502818943139http://lattes.cnpq.br/5833091143764435Zambiazi, Priscilla Jussiane1006000000004005003003005007e7796b1-053d-4bbe-8e62-e769f0da5cea362da7d8-5946-4f2b-8ecd-f9f5df3600af455eae8e-d46f-4e15-8c0d-249c48314f836c576d48-34e1-4008-b46b-a68350c55a17info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALZAMBIAZI, PRISCILA JUSSIANE.pdfapplication/pdf10163252http://repositorio.ufsm.br/bitstream/1/10543/1/ZAMBIAZI%2c%20PRISCILA%20JUSSIANE.pdf0fe47a1bd4ebf627a10d16cfcd6804b6MD51TEXTZAMBIAZI, PRISCILA JUSSIANE.pdf.txtZAMBIAZI, PRISCILA JUSSIANE.pdf.txtExtracted texttext/plain212051http://repositorio.ufsm.br/bitstream/1/10543/2/ZAMBIAZI%2c%20PRISCILA%20JUSSIANE.pdf.txt27706e2a3ddce58c6189004886aee50aMD52THUMBNAILZAMBIAZI, PRISCILA JUSSIANE.pdf.jpgZAMBIAZI, PRISCILA JUSSIANE.pdf.jpgIM Thumbnailimage/jpeg5765http://repositorio.ufsm.br/bitstream/1/10543/3/ZAMBIAZI%2c%20PRISCILA%20JUSSIANE.pdf.jpgb8de3a9c3303e4e48bea2c2e1c651801MD531/105432022-05-11 10:37:26.437oai:repositorio.ufsm.br:1/10543Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2022-05-11T13:37:26Biblioteca Digital de Teses e Dissertações do UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.por.fl_str_mv Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
dc.title.alternative.eng.fl_str_mv Synthesis, crystallographic analysis and biological activity of the complexes with triazenides ligands with orto-halophenyl and para-sulfonamidephenyl fragments
title Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
spellingShingle Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
Zambiazi, Priscilla Jussiane
Triazenos
Complexos de Pd(II)
K+ e Au(I)
Synthons supramoleculares
Interações halogênio···halogênio
Atividade biológica
Triazenes
Complexes of Pd(II)
K+ and Au(I)
Supramolecular synthons
Halogen···halogen interactions
Biological activity
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
title_full Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
title_fullStr Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
title_full_unstemmed Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
title_sort Síntese, análise cristalográfica e atividade biológica de complexos com ligantes triazenidos com fragmentos orto-halofenila e para-sulfonamidafenila
author Zambiazi, Priscilla Jussiane
author_facet Zambiazi, Priscilla Jussiane
author_role author
dc.contributor.advisor1.fl_str_mv Hörner, Manfredo
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/8922528250830998
dc.contributor.referee1.fl_str_mv Bresolin, Leandro
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/3961672079507969
dc.contributor.referee2.fl_str_mv Squizani, Fatima
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/1060502818943139
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/5833091143764435
dc.contributor.author.fl_str_mv Zambiazi, Priscilla Jussiane
contributor_str_mv Hörner, Manfredo
Bresolin, Leandro
Squizani, Fatima
dc.subject.por.fl_str_mv Triazenos
Complexos de Pd(II)
K+ e Au(I)
Synthons supramoleculares
Interações halogênio···halogênio
Atividade biológica
topic Triazenos
Complexos de Pd(II)
K+ e Au(I)
Synthons supramoleculares
Interações halogênio···halogênio
Atividade biológica
Triazenes
Complexes of Pd(II)
K+ and Au(I)
Supramolecular synthons
Halogen···halogen interactions
Biological activity
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Triazenes
Complexes of Pd(II)
K+ and Au(I)
Supramolecular synthons
Halogen···halogen interactions
Biological activity
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description This study shows the triazenes ligands and complexes Pd(II), K+ and Au(I) obtained from reactions of the ligands with fragments para-sulfonamidephenyl, comprising triazene ligand 1,3-bis (4 - sulfonamidephenyl) (1) and the complex {trans-Bis[1,3-bis(4-sulfonamidephenyl)triazenide-κN1]bis(pyridine-κN)palladium(II)}{tetra(pyridine-κN)palladium(II)}bis(potssium)·water (2) and for compounds containing orto-halophenyl fragments represented by [1,3-bis(2-fluorophenyl)triazenide-κN1](triphenylphosphine- κP)gold(I) (3), [1,3-bis(2-chlorinephenyl)triazenide-κN1](triphenylphosphine-κP)gold(I) (4), [1,3-bis(2-bromidephenyl)triazenide-κN1](triphenylphosphine-κP)gold(I) (5) and [1,3-bis(2-iodinephenyl)triazenide-κN1](triphenylphosphine - κP)gold(I) (6) complexes. The compounds reported were characterized by X-ray diffraction on single crystal, and their structures in solid state are formed through supramolecular arrangements via classical and non-classical hydrogen bonding, as in the case of the compounds with the sulfonamide grouping, one can observe the formation of supramolecular synthons. In complexes 4, 5 and 6 it is observed to occur interactions halogen···halogen characterized by the formation of dimeric units associated by a center of inversion, besides having geometries classified by the angle of the links formed between the halogen and carbon atoms. Compounds 1, 2, 3, 4, 5 and 6 were subjected to evaluation front of biological activity, such as plasmidial DNA cleavage studies, evaluation of cytotoxicity and antibacterial activity, showing promising results.
publishDate 2013
dc.date.issued.fl_str_mv 2013-03-08
dc.date.accessioned.fl_str_mv 2017-05-22
dc.date.available.fl_str_mv 2017-05-22
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dc.identifier.citation.fl_str_mv ZAMBIAZI, Priscilla Jussiane. Synthesis, crystallographic analysis and biological activity of the complexes with triazenides ligands with orto-halophenyl and para-sulfonamidephenyl fragments. 2013. 168 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2013.
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/10543
identifier_str_mv ZAMBIAZI, Priscilla Jussiane. Synthesis, crystallographic analysis and biological activity of the complexes with triazenides ligands with orto-halophenyl and para-sulfonamidephenyl fragments. 2013. 168 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2013.
url http://repositorio.ufsm.br/handle/1/10543
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