Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)

Detalhes bibliográficos
Autor(a) principal: Broch, Fernanda
Data de Publicação: 2008
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
Texto Completo: http://repositorio.ufsm.br/handle/1/10428
Resumo: Triazenes and/or triazenido ligands, strategically substituted by terminal aryl groups [-N=NN(H)-] or (-N3 --) chains and containing halogen in the ortho position and ester in the para position, were evaluated in relation to the occurrence of intermolecular interactions through secondary non-covalent bonding. The research is based on the single crystal X-ray diffraction to analysis of arrangements performed by the free triazene molecules and by the triazenido complexes in the solid state. Triazenido ligands show a variety of modes of coordination which has motivated several structural studies of free triazenes and related complexes with diverse transition metals. This work report the synthesis and crystal structure of five new molecules in the literature: 1-(2-chlorophenyl)-3-(4-ethoxycarbonylphenyl)triazene; 1-(2-bromophenyl)-3-(4-ethoxycarbonylphenyl)triazene, and the mononuclear complexes bis[1-(4-ethoxycabonylphenyl)-3-(2-fluorophenyl)- triazenide]mercury(II), cis-bis[3-(2-fluorophenyl)-1-(4-carboxyphenyl)triazenide]-bis(pyridine)- nickel(II) and trans-bis[3-(2-iodophenyl)-1-(4-carboxyphenyl)triazenide]-bis(pyridine) copper(II). The asymmetric diaryltriazene molecules, Ar-NNNH-Ar [Ar = o-C6H4-X (X=F, Cl, Br, I); Ar = p-C6H4-CO2Et] and the related complexes were obtained in good yields in accordance with the reaction conditions of similar compounds reported in literarure. Beside the structural analysis of al compounds, melting-point, infrared, nuclear magnetic resonance and ultraviolet-visible espectroscopies wer also carried out for characterization.
id UFSM_72f40d72a401b4bf85c719beb4bbb322
oai_identifier_str oai:repositorio.ufsm.br:1/10428
network_acronym_str UFSM
network_name_str Manancial - Repositório Digital da UFSM
repository_id_str
spelling Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)Supramolecularity of asymmetric disubstituted 4-(ethoxycarbonylphenyl)-2-(halophenyl)triazenes and complexes containing Ni(II), Cu(II), and Hg(II)TriazenoComplexos triazenidosDifração de raios-XArranjo supramolecularTriazeneTriazenide complexX-ray diffractionSupramolecular arrangementCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICATriazenes and/or triazenido ligands, strategically substituted by terminal aryl groups [-N=NN(H)-] or (-N3 --) chains and containing halogen in the ortho position and ester in the para position, were evaluated in relation to the occurrence of intermolecular interactions through secondary non-covalent bonding. The research is based on the single crystal X-ray diffraction to analysis of arrangements performed by the free triazene molecules and by the triazenido complexes in the solid state. Triazenido ligands show a variety of modes of coordination which has motivated several structural studies of free triazenes and related complexes with diverse transition metals. This work report the synthesis and crystal structure of five new molecules in the literature: 1-(2-chlorophenyl)-3-(4-ethoxycarbonylphenyl)triazene; 1-(2-bromophenyl)-3-(4-ethoxycarbonylphenyl)triazene, and the mononuclear complexes bis[1-(4-ethoxycabonylphenyl)-3-(2-fluorophenyl)- triazenide]mercury(II), cis-bis[3-(2-fluorophenyl)-1-(4-carboxyphenyl)triazenide]-bis(pyridine)- nickel(II) and trans-bis[3-(2-iodophenyl)-1-(4-carboxyphenyl)triazenide]-bis(pyridine) copper(II). The asymmetric diaryltriazene molecules, Ar-NNNH-Ar [Ar = o-C6H4-X (X=F, Cl, Br, I); Ar = p-C6H4-CO2Et] and the related complexes were obtained in good yields in accordance with the reaction conditions of similar compounds reported in literarure. Beside the structural analysis of al compounds, melting-point, infrared, nuclear magnetic resonance and ultraviolet-visible espectroscopies wer also carried out for characterization.Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorTriazenos e/ou ligantes triazenidos, estrategicamente substituídos por grupos arilas terminais na cadeia diazoamínica [-N=N-N(H)-] ou triazenídica (-N3 --) contendo halogênio na posição orto e éster na posição para, foram avaliados quanto à ocorrência de interações intermoleculares através de ligações secundárias não-covalentes. A investigação baseou-se principalmente na difração de raios-X em monocristal para analisar estruturalmente a formação de arranjos supramoleculares formados pelas moléculas e complexos no estado sólido. Ligantes triazenidos apresentam uma variedade de modos de coordenação os quais tem motivado vários estudos estruturais desses compostos nas moléculas livres e em complexos com metais de transição. Sob este ponto de vista, apresenta-se neste trabalho a síntese e a investigação da estrutura cristalina e molecular de cinco moléculas inéditas na literatura: os pré-ligantes 1-(2-clorofenil)-3-(4-etoxicarbonilfenil)triazeno; 1-(2-bromofenil)-3- (4-etoxicarbonilfenil)triazeno, e dos complexos mononucleares bis[1-(4-etoxicabonilfenil)-3-(2-fluorofenil)triazenido]mercúrio(II); cis-bis[3-(2-fluorofenil)-1-(4-etoxicarbonilfenil)triazenido]- bis (piridina)níquel(II) e trans-bis[3-(2-iodofenil)-1-(4-etoxicarbonilfenil)triazenido]-bis(piridina)cobre(II). Os ligantes bis(aril)triazenos, Ar-NNNH-Ar [Ar = o-C6H4-X (X=F, Cl, Br, I); Ar = p- C6H4-CO2Et] e os complexos foram preparados com bons rendimentos de acordo com condições padrões relatadas na literarura. Técnicas de ponto de fusão, espectroscopias de infravermelho, ressonância magnética nuclear e na região do ultravioleta-visível complementaram o trabalho.Universidade Federal de Santa MariaBRQuímicaUFSMPrograma de Pós-Graduação em QuímicaHörner, Manfredohttp://lattes.cnpq.br/8922528250830998Nunes, Fabio Souzahttp://lattes.cnpq.br/7117607785614286Squizani, Fatimahttp://lattes.cnpq.br/1060502818943139Broch, Fernanda2017-05-162017-05-162008-05-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfBROCH, Fernanda. Supramolecularity of asymmetric disubstituted 4-(ethoxycarbonylphenyl)-2-(halophenyl)triazenes and complexes containing Ni(II), Cu(II), and Hg(II). 2008. 141 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2008.http://repositorio.ufsm.br/handle/1/10428porinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2023-04-17T17:18:14Zoai:repositorio.ufsm.br:1/10428Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2023-04-17T17:18:14Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
Supramolecularity of asymmetric disubstituted 4-(ethoxycarbonylphenyl)-2-(halophenyl)triazenes and complexes containing Ni(II), Cu(II), and Hg(II)
title Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
spellingShingle Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
Broch, Fernanda
Triazeno
Complexos triazenidos
Difração de raios-X
Arranjo supramolecular
Triazene
Triazenide complex
X-ray diffraction
Supramolecular arrangement
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
title_full Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
title_fullStr Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
title_full_unstemmed Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
title_sort Supramolecularidade de triazenos assimétricos dissubstituídos 4-(etoxicarbonilfenil)-2-(halofenil) e complexos de Ni(II), Cu(II) e Hg(II)
author Broch, Fernanda
author_facet Broch, Fernanda
author_role author
dc.contributor.none.fl_str_mv Hörner, Manfredo
http://lattes.cnpq.br/8922528250830998
Nunes, Fabio Souza
http://lattes.cnpq.br/7117607785614286
Squizani, Fatima
http://lattes.cnpq.br/1060502818943139
dc.contributor.author.fl_str_mv Broch, Fernanda
dc.subject.por.fl_str_mv Triazeno
Complexos triazenidos
Difração de raios-X
Arranjo supramolecular
Triazene
Triazenide complex
X-ray diffraction
Supramolecular arrangement
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
topic Triazeno
Complexos triazenidos
Difração de raios-X
Arranjo supramolecular
Triazene
Triazenide complex
X-ray diffraction
Supramolecular arrangement
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description Triazenes and/or triazenido ligands, strategically substituted by terminal aryl groups [-N=NN(H)-] or (-N3 --) chains and containing halogen in the ortho position and ester in the para position, were evaluated in relation to the occurrence of intermolecular interactions through secondary non-covalent bonding. The research is based on the single crystal X-ray diffraction to analysis of arrangements performed by the free triazene molecules and by the triazenido complexes in the solid state. Triazenido ligands show a variety of modes of coordination which has motivated several structural studies of free triazenes and related complexes with diverse transition metals. This work report the synthesis and crystal structure of five new molecules in the literature: 1-(2-chlorophenyl)-3-(4-ethoxycarbonylphenyl)triazene; 1-(2-bromophenyl)-3-(4-ethoxycarbonylphenyl)triazene, and the mononuclear complexes bis[1-(4-ethoxycabonylphenyl)-3-(2-fluorophenyl)- triazenide]mercury(II), cis-bis[3-(2-fluorophenyl)-1-(4-carboxyphenyl)triazenide]-bis(pyridine)- nickel(II) and trans-bis[3-(2-iodophenyl)-1-(4-carboxyphenyl)triazenide]-bis(pyridine) copper(II). The asymmetric diaryltriazene molecules, Ar-NNNH-Ar [Ar = o-C6H4-X (X=F, Cl, Br, I); Ar = p-C6H4-CO2Et] and the related complexes were obtained in good yields in accordance with the reaction conditions of similar compounds reported in literarure. Beside the structural analysis of al compounds, melting-point, infrared, nuclear magnetic resonance and ultraviolet-visible espectroscopies wer also carried out for characterization.
publishDate 2008
dc.date.none.fl_str_mv 2008-05-02
2017-05-16
2017-05-16
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv BROCH, Fernanda. Supramolecularity of asymmetric disubstituted 4-(ethoxycarbonylphenyl)-2-(halophenyl)triazenes and complexes containing Ni(II), Cu(II), and Hg(II). 2008. 141 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2008.
http://repositorio.ufsm.br/handle/1/10428
identifier_str_mv BROCH, Fernanda. Supramolecularity of asymmetric disubstituted 4-(ethoxycarbonylphenyl)-2-(halophenyl)triazenes and complexes containing Ni(II), Cu(II), and Hg(II). 2008. 141 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2008.
url http://repositorio.ufsm.br/handle/1/10428
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
BR
Química
UFSM
Programa de Pós-Graduação em Química
publisher.none.fl_str_mv Universidade Federal de Santa Maria
BR
Química
UFSM
Programa de Pós-Graduação em Química
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
_version_ 1805922038633725952