Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas

Detalhes bibliográficos
Ano de defesa: 2016
Autor(a) principal: Mota, João Paulo Ferreira
Orientador(a): Mazzetto, Selma Elaine
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Não Informado pela instituição
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://www.repositorio.ufc.br/handle/riufc/40132
Resumo: In this study were obtained some macromolecules, new asymmetric meso-porphyrins and phthalocyanines, derived from hydrogenated cardanol, the majority constituent of the cashew nut shell liquid (technical CNSL). Where, in addition, it was evaluated the liquid crystalline properties of these compounds in heating and cooling cycles. The data obtained by spectroscopic and spectrometric methods, 1H and 13C NMR, UV-vis, MS (MALDI-TOF) and IR have indicated the efficiency of the synthetic procedure, that allowed us, to obtain the new meso-5-mono-4-hydroxyphenyl-10,15,20-tri-4-[2-(3-pentadecylphenoxy)ethoxy]phenyl porphyrin free and metalated with nickel, cobalt, copper and zinc, as well as the 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecylphenoxy) phthalocyanine free and metallated with cobalt, nickel, zinc and copper. The precursors produced in this study, 1-(2- bromoethoxy)-3-pentadecylbenzene (compound 1), 4-[2-(3-pentadecylphenoxy)ethoxy] benzaldehyde (compound 2) e 4-(3-pentadecylphenoxy)phthalonitrile (compound 3), were purified by two different procedures: column chromatography (a) and recrystallization (b). Whereas for the last, a significant reduction in the generation of residues were observed, when comparing the chromatography, which on average, 200 g of silica gel and 1650 mL of solvent were used. The liquid crystalline properties of the macromolecules were measured by means of images obtained in polarized optical microscopy (POM), during heating and cooling cycles. These images show that only free phthalocyanine 2(3),9(10),16(17),23(24)-tetrakis(-3- pentadecylphenoxy) self-organizes, displaying focal conic textures, which were observed in liquid crystal phases. Another compound that showed evidence of an organized phase was the cobalt 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecylphenoxy) phthalocyanine. However, the results of X-rays diffraction analysis suggest that only the free phthalocyanine showed the formation of a liquid crystalline phase with discotic hexagonal columnar structure (Colh).
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spelling Mota, João Paulo FerreiraMazzetto, Selma Elaine2019-03-07T18:36:50Z2019-03-07T18:36:50Z2016MOTA, João Paulo Ferreira. Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas. 2016. 110 f. Tese (Doutorado em Química) - Universidade Federal do Ceará, Fortaleza, 2016.http://www.repositorio.ufc.br/handle/riufc/40132In this study were obtained some macromolecules, new asymmetric meso-porphyrins and phthalocyanines, derived from hydrogenated cardanol, the majority constituent of the cashew nut shell liquid (technical CNSL). Where, in addition, it was evaluated the liquid crystalline properties of these compounds in heating and cooling cycles. The data obtained by spectroscopic and spectrometric methods, 1H and 13C NMR, UV-vis, MS (MALDI-TOF) and IR have indicated the efficiency of the synthetic procedure, that allowed us, to obtain the new meso-5-mono-4-hydroxyphenyl-10,15,20-tri-4-[2-(3-pentadecylphenoxy)ethoxy]phenyl porphyrin free and metalated with nickel, cobalt, copper and zinc, as well as the 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecylphenoxy) phthalocyanine free and metallated with cobalt, nickel, zinc and copper. The precursors produced in this study, 1-(2- bromoethoxy)-3-pentadecylbenzene (compound 1), 4-[2-(3-pentadecylphenoxy)ethoxy] benzaldehyde (compound 2) e 4-(3-pentadecylphenoxy)phthalonitrile (compound 3), were purified by two different procedures: column chromatography (a) and recrystallization (b). Whereas for the last, a significant reduction in the generation of residues were observed, when comparing the chromatography, which on average, 200 g of silica gel and 1650 mL of solvent were used. The liquid crystalline properties of the macromolecules were measured by means of images obtained in polarized optical microscopy (POM), during heating and cooling cycles. These images show that only free phthalocyanine 2(3),9(10),16(17),23(24)-tetrakis(-3- pentadecylphenoxy) self-organizes, displaying focal conic textures, which were observed in liquid crystal phases. Another compound that showed evidence of an organized phase was the cobalt 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecylphenoxy) phthalocyanine. However, the results of X-rays diffraction analysis suggest that only the free phthalocyanine showed the formation of a liquid crystalline phase with discotic hexagonal columnar structure (Colh).Neste trabalho foram obtidas algumas macromoléculas, novas meso-porfirinas assimétricas e ftalocianinas, derivadas do cardanol hidrogenado, o constituinte majoritário do Líquido da Casca da Castanha de Caju (LCC técnico). Onde, além disso, foi avaliado as propriedades liquido cristalinas destes compostos em ciclos de aquecimento e resfriamento. Os dados obtidos por meio de métodos espectroscópicos e espectrométricos, RMN 1H e 13C, UV−vis, EM (Maldi−TOF) e IV, indicaram a eficiencia do procedimento sintético que possibilitou obter a nova meso-5-mono-4-hidroxifenil-10,15,20-tri-4-[2-(3-pentadecilfenoxi)etoxi]fenil porfirina livre e metalada com níquel, cobalto, cobre e zinco, bem como a 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecilfenoxi) ftalocianina livre e metalada com cobalto, níquel, zinco e cobre. Os precursores produzidos neste trabalho, 1-(2-bromoetoxi)-3- pentadecilbenzeno (composto 1), 4-[2-(3-pentadecilfenoxi) etoxi]benzaldeido (composto 2) e 4-(3-pentadecilfenoxi)ftalonitrila (composto 3), foram purificados por dois procedimentos distintos: cromatografia em coluna (a) e recristalização (b). Sendo que no último, foi observado uma redução significativa na geração de resíduos, quando comparamos esta metodologia com a cromatográfia em coluna, onde em média 200 g de gel de sílica e 1650 mL de solvente foram utilizados. As propriedades liquido cristalinas das macromoléculas foram avaliadas por meio de imagens obtidas na microscopia óptica de luz polarizada (MOLP) em ciclos de aquecimento e resfriamento. Estas imagens mostraram que apenas a ftalocianina 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecilfenoxi) livre se auto-organiza exibindo texturas cônica focal, a qual é observada em fases liquido cristalinas. Outro composto que apresentou indícios de uma fase organizada foi a cobalto 2(3),9(10),16(17),23(24)-tetrakis(-3- pentadecilfenoxi) ftalocianina. No entanto, os resultados das análises de difração de raios-X sugerem que apenas a ftalocianina livre apresentou a formação de uma fase líquido cristalina com estrutura discótica colunar hexagonal (Colh).Porfirinas assimétricasFtalocianinasCristal líquidoLCC técnicoRecristalizaçãoMacromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinasinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisporreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccessORIGINAL2016_tese_jpfmota.pdf2016_tese_jpfmota.pdfapplication/pdf4198943http://repositorio.ufc.br/bitstream/riufc/40132/1/2016_tese_jpfmota.pdff4c5be943179e657d9c041f64408b72dMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://repositorio.ufc.br/bitstream/riufc/40132/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52riufc/401322019-03-07 15:36:50.105oai:repositorio.ufc.br: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Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2019-03-07T18:36:50Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.pt_BR.fl_str_mv Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
title Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
spellingShingle Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
Mota, João Paulo Ferreira
Porfirinas assimétricas
Ftalocianinas
Cristal líquido
LCC técnico
Recristalização
title_short Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
title_full Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
title_fullStr Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
title_full_unstemmed Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
title_sort Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas
author Mota, João Paulo Ferreira
author_facet Mota, João Paulo Ferreira
author_role author
dc.contributor.author.fl_str_mv Mota, João Paulo Ferreira
dc.contributor.advisor1.fl_str_mv Mazzetto, Selma Elaine
contributor_str_mv Mazzetto, Selma Elaine
dc.subject.por.fl_str_mv Porfirinas assimétricas
Ftalocianinas
Cristal líquido
LCC técnico
Recristalização
topic Porfirinas assimétricas
Ftalocianinas
Cristal líquido
LCC técnico
Recristalização
description In this study were obtained some macromolecules, new asymmetric meso-porphyrins and phthalocyanines, derived from hydrogenated cardanol, the majority constituent of the cashew nut shell liquid (technical CNSL). Where, in addition, it was evaluated the liquid crystalline properties of these compounds in heating and cooling cycles. The data obtained by spectroscopic and spectrometric methods, 1H and 13C NMR, UV-vis, MS (MALDI-TOF) and IR have indicated the efficiency of the synthetic procedure, that allowed us, to obtain the new meso-5-mono-4-hydroxyphenyl-10,15,20-tri-4-[2-(3-pentadecylphenoxy)ethoxy]phenyl porphyrin free and metalated with nickel, cobalt, copper and zinc, as well as the 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecylphenoxy) phthalocyanine free and metallated with cobalt, nickel, zinc and copper. The precursors produced in this study, 1-(2- bromoethoxy)-3-pentadecylbenzene (compound 1), 4-[2-(3-pentadecylphenoxy)ethoxy] benzaldehyde (compound 2) e 4-(3-pentadecylphenoxy)phthalonitrile (compound 3), were purified by two different procedures: column chromatography (a) and recrystallization (b). Whereas for the last, a significant reduction in the generation of residues were observed, when comparing the chromatography, which on average, 200 g of silica gel and 1650 mL of solvent were used. The liquid crystalline properties of the macromolecules were measured by means of images obtained in polarized optical microscopy (POM), during heating and cooling cycles. These images show that only free phthalocyanine 2(3),9(10),16(17),23(24)-tetrakis(-3- pentadecylphenoxy) self-organizes, displaying focal conic textures, which were observed in liquid crystal phases. Another compound that showed evidence of an organized phase was the cobalt 2(3),9(10),16(17),23(24)-tetrakis(-3-pentadecylphenoxy) phthalocyanine. However, the results of X-rays diffraction analysis suggest that only the free phthalocyanine showed the formation of a liquid crystalline phase with discotic hexagonal columnar structure (Colh).
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2019-03-07T18:36:50Z
dc.date.available.fl_str_mv 2019-03-07T18:36:50Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
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dc.identifier.citation.fl_str_mv MOTA, João Paulo Ferreira. Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas. 2016. 110 f. Tese (Doutorado em Química) - Universidade Federal do Ceará, Fortaleza, 2016.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufc.br/handle/riufc/40132
identifier_str_mv MOTA, João Paulo Ferreira. Macromoléculas derivadas do cardanol hidrogenado: síntese e propriedades líquido cristalinas. 2016. 110 f. Tese (Doutorado em Química) - Universidade Federal do Ceará, Fortaleza, 2016.
url http://www.repositorio.ufc.br/handle/riufc/40132
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