Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina

Detalhes bibliográficos
Ano de defesa: 2012
Autor(a) principal: Martins, Tássia Joi
Orientador(a): Moreira, Wania da Conceição lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de São Carlos
Programa de Pós-Graduação: Programa de Pós-Graduação em Química - PPGQ
Departamento: Não Informado pela instituição
País: BR
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.ufscar.br/handle/ufscar/6519
Resumo: Metalloporphyrins and metalophthalocyanines assemblies have attracted in the last few decades. The syntheses of face to face systems containing porphyrins or phthalocyanines can found in literature, however few works reported these arrangements in mixed systems. A new system composed by cobaltophthalocyanine (CoPc) and cobaltotetraphenylporphyrin (CoTPP) assembled in a face to face arrangement by using a rigid and conjugate ligand, like pyrazine (pyz), may result in a new material with interesting properties. Recently, in our laboratory, a new synthetic route for mixed complexes like CoPc(pyz)CoTPP(pyz)CoPc and CoTPP(pyz)CoPc(pyz)CoTPP was developed. Nevertheless, the possibility of an increase in the chain has not been investigated. This work aimed the investigation of a synthesis of heteropentamers formed by metaloporphyrins and metalophthalocyanines complexes, relating their properties with precursor s complexes. The heteropentamers synthesis was carried out using the same methodology described for heterotriads. It was synthesized the follow sequences of heteropentamers: CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc 2, CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP 1 and 2. For each synthesis, two fractions were obtained and isolated. The characterization was carried out by vibrational spectroscopy, Uv-vis spectroscopy, thermal analyses and solubility tests. The vibrational spectra showed the coordination of the macrocycles to the pyrazine terminal ligands on the adducts. This was also observed by thermogravimetry analysis. By the thermal analysis was also possible to verify differences in binding between the terminal pyrazines and the internal pyrazine ligands. The electronic spectra of heteropentamers showed chacacteristic bands of each macrocycle, however were observed shifts in the absorption bands of phthalocyanines and porphyrins in the heteropentamers fractions.
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spelling Martins, Tássia JoiMoreira, Wania da Conceiçãohttp://genos.cnpq.br:12010/dwlattes/owa/prc_imp_cv_int?f_cod=K4786312J8http://lattes.cnpq.br/77206334415687762016-06-02T20:36:37Z2012-04-202016-06-02T20:36:37Z2012-02-29https://repositorio.ufscar.br/handle/ufscar/6519Metalloporphyrins and metalophthalocyanines assemblies have attracted in the last few decades. The syntheses of face to face systems containing porphyrins or phthalocyanines can found in literature, however few works reported these arrangements in mixed systems. A new system composed by cobaltophthalocyanine (CoPc) and cobaltotetraphenylporphyrin (CoTPP) assembled in a face to face arrangement by using a rigid and conjugate ligand, like pyrazine (pyz), may result in a new material with interesting properties. Recently, in our laboratory, a new synthetic route for mixed complexes like CoPc(pyz)CoTPP(pyz)CoPc and CoTPP(pyz)CoPc(pyz)CoTPP was developed. Nevertheless, the possibility of an increase in the chain has not been investigated. This work aimed the investigation of a synthesis of heteropentamers formed by metaloporphyrins and metalophthalocyanines complexes, relating their properties with precursor s complexes. The heteropentamers synthesis was carried out using the same methodology described for heterotriads. It was synthesized the follow sequences of heteropentamers: CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc 2, CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP 1 and 2. For each synthesis, two fractions were obtained and isolated. The characterization was carried out by vibrational spectroscopy, Uv-vis spectroscopy, thermal analyses and solubility tests. The vibrational spectra showed the coordination of the macrocycles to the pyrazine terminal ligands on the adducts. This was also observed by thermogravimetry analysis. By the thermal analysis was also possible to verify differences in binding between the terminal pyrazines and the internal pyrazine ligands. The electronic spectra of heteropentamers showed chacacteristic bands of each macrocycle, however were observed shifts in the absorption bands of phthalocyanines and porphyrins in the heteropentamers fractions.O estudo das propriedades de materiais obtidos pela automontagem tendo como elementos constituintes metaloporfirinas e metaloftalocianinas tem despertado um crescente interesse nas últimas décadas. São descritos em literatura algumas sínteses de sistemas face a face contendo porfirinas ou ftalocianinas, porém poucos trabalhos descrevem esses arranjos moleculares mistos. Portanto, a proposta de um novo sistema composto por complexos ftalocianina (CoPc) e porfirinas (CoTPP) ligados por um ligante rígido e conjugado, como a pirazina (pyz), se torna interessante. Recentemente, em nosso laboratório, uma rota sintética para sistemas mistos do tipo CoPc(pyz)CoTPP(pyz)CoPc e CoTPP(pyz)CoPc(pyz)CoTPP foi desenvolvida. Entretanto, a possibilidade de aumento da cadeia ainda não foi investigada. Assim, este trabalho teve como objetivo principal investigar a possibilidade de síntese de heteropentâmeros formados por complexos de metaloftalocianinas e metaloporfirinas e o efeito do aumento da cadeia, relacionando suas propriedades com os complexos precursores. Para a síntese dos heteropentâmeros foi utilizada a metodologia desenvolvida em nosso laboratório para heterotríades. Foram sintetizadas as seguintes sequências de heteropentâmeros: CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc 2, CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP 1 e 2, obtendo duas frações de cada sequência. A caracterização dos heteropentâmeros foi realizada através de espectroscopia vibracional (FTIR e espectroscopia Raman), espectroscopia eletrônica na região Uv-vis, análises térmicas, além de testes de solubilidade. A análise dos espectros vibracionais dos adutos demonstrou que bandas do ligante pirazina, após a formação dos heteropentâmeros não podem ser visualizadas, devido à coordenação dos complexos terminais. As análises termogravimétricas demonstraram diferenças na coordenação dos ligantes pirazina terminais e os ligantes mais internos no aduto, o que corrobora com as observações por espectroscopia vibracional. Os espectros eletrônicos dos heteropentâmeros apresentaram bandas características das unidades componentes desses sistemas, porém foram observados deslocamentos nas bandas xiii características das porfirinas e ftalocianinas nas diferentes frações de heteropentâmeros.Financiadora de Estudos e Projetosapplication/pdfporUniversidade Federal de São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarBRQuímica inorgânicaMetaloftalocianinaMetaloporfirinasComplexos mistosPropriedades eletrônicasCIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICASíntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirinainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINAL4252.pdfapplication/pdf1683521https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/6519/1/4252.pdfcbfeafe69fd4e87a641ef7d74f2d3006MD51TEXT4252.pdf.txt4252.pdf.txtExtracted texttext/plain0https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/6519/4/4252.pdf.txtd41d8cd98f00b204e9800998ecf8427eMD54THUMBNAIL4252.pdf.jpg4252.pdf.jpgIM Thumbnailimage/jpeg9048https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/6519/5/4252.pdf.jpg2f8bface6cdf842332c57b4b96671e6aMD55ufscar/65192020-03-23 19:52:13.702oai:repositorio.ufscar.br:ufscar/6519Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-05-25T12:51:23.344483Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
title Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
spellingShingle Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
Martins, Tássia Joi
Química inorgânica
Metaloftalocianina
Metaloporfirinas
Complexos mistos
Propriedades eletrônicas
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA
title_short Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
title_full Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
title_fullStr Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
title_full_unstemmed Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
title_sort Síntese e caracterização de heteropentâmeros formados por cobaltoftalocianina e cobaltotetrafenilporfirina
author Martins, Tássia Joi
author_facet Martins, Tássia Joi
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/7720633441568776
dc.contributor.author.fl_str_mv Martins, Tássia Joi
dc.contributor.advisor1.fl_str_mv Moreira, Wania da Conceição
dc.contributor.advisor1Lattes.fl_str_mv http://genos.cnpq.br:12010/dwlattes/owa/prc_imp_cv_int?f_cod=K4786312J8
contributor_str_mv Moreira, Wania da Conceição
dc.subject.por.fl_str_mv Química inorgânica
Metaloftalocianina
Metaloporfirinas
Complexos mistos
Propriedades eletrônicas
topic Química inorgânica
Metaloftalocianina
Metaloporfirinas
Complexos mistos
Propriedades eletrônicas
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA
description Metalloporphyrins and metalophthalocyanines assemblies have attracted in the last few decades. The syntheses of face to face systems containing porphyrins or phthalocyanines can found in literature, however few works reported these arrangements in mixed systems. A new system composed by cobaltophthalocyanine (CoPc) and cobaltotetraphenylporphyrin (CoTPP) assembled in a face to face arrangement by using a rigid and conjugate ligand, like pyrazine (pyz), may result in a new material with interesting properties. Recently, in our laboratory, a new synthetic route for mixed complexes like CoPc(pyz)CoTPP(pyz)CoPc and CoTPP(pyz)CoPc(pyz)CoTPP was developed. Nevertheless, the possibility of an increase in the chain has not been investigated. This work aimed the investigation of a synthesis of heteropentamers formed by metaloporphyrins and metalophthalocyanines complexes, relating their properties with precursor s complexes. The heteropentamers synthesis was carried out using the same methodology described for heterotriads. It was synthesized the follow sequences of heteropentamers: CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc 2, CoTPP(pyz)CoPc(pyz)CoTPP(pyz)CoPc(pyz)CoTPP 1 and 2. For each synthesis, two fractions were obtained and isolated. The characterization was carried out by vibrational spectroscopy, Uv-vis spectroscopy, thermal analyses and solubility tests. The vibrational spectra showed the coordination of the macrocycles to the pyrazine terminal ligands on the adducts. This was also observed by thermogravimetry analysis. By the thermal analysis was also possible to verify differences in binding between the terminal pyrazines and the internal pyrazine ligands. The electronic spectra of heteropentamers showed chacacteristic bands of each macrocycle, however were observed shifts in the absorption bands of phthalocyanines and porphyrins in the heteropentamers fractions.
publishDate 2012
dc.date.available.fl_str_mv 2012-04-20
2016-06-02T20:36:37Z
dc.date.issued.fl_str_mv 2012-02-29
dc.date.accessioned.fl_str_mv 2016-06-02T20:36:37Z
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