Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos

Detalhes bibliográficos
Autor(a) principal: Kautz, Jacqueline
Data de Publicação: 2015
Outros Autores: Feltrin, Carlos Willian, Sales, Eric Souza, Eifler-Lima, Vera Lucia, Merlo, Aloir Antonio
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/131116
Resumo: Condensation reactions of glycerol with aldehydes and ketones were performed under thermal heating and microwave irradiation regimes. Homogeneous and heterogeneous catalysts were tested in both conditions. A silica sulfated (SiO2–SO3H) heterogeneous catalyst demonstrated the best performance relative to a selectivity of >95% in favor of 5-membered ketals. For acetals, preference in favor of 5-membered or 6-membered functional groups depends on the nature of the catalyst. Homogenous catalysts favor the more stable 6-membered acetals, whereas heterogeneous catalysts favor the less stable 5-membered acetals. However, the isomer ratios in the acetalization reaction are too low, and hence the reaction cannot be used in a synthetic plan for functional materials. Ketalization processes mediated by SiO2–SO3H show a high selectivity in favor of a 5-membered ring (1,3-dioxolane). The scope of condensation was tested with different ketones. A mechanism for heterogeneous catalysis related to the selectivity in the cyclization process is presented herein. Solketal, a commercial product, was also obtained by a condensation reaction of glycerol and propanone, and showed a high selectivity in favor of 1,3-dioxolane. It was transformed to potential allylic and chiral intermediates. A mesogenic core was connected to the organic framework of glycerol to produce a monomer liquid crystal material with a stable smectic-C mesophase.
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spelling Kautz, JacquelineFeltrin, Carlos WillianSales, Eric SouzaEifler-Lima, Vera LuciaMerlo, Aloir Antonio2015-12-15T02:37:47Z20150100-4042http://hdl.handle.net/10183/131116000980570Condensation reactions of glycerol with aldehydes and ketones were performed under thermal heating and microwave irradiation regimes. Homogeneous and heterogeneous catalysts were tested in both conditions. A silica sulfated (SiO2–SO3H) heterogeneous catalyst demonstrated the best performance relative to a selectivity of >95% in favor of 5-membered ketals. For acetals, preference in favor of 5-membered or 6-membered functional groups depends on the nature of the catalyst. Homogenous catalysts favor the more stable 6-membered acetals, whereas heterogeneous catalysts favor the less stable 5-membered acetals. However, the isomer ratios in the acetalization reaction are too low, and hence the reaction cannot be used in a synthetic plan for functional materials. Ketalization processes mediated by SiO2–SO3H show a high selectivity in favor of a 5-membered ring (1,3-dioxolane). The scope of condensation was tested with different ketones. A mechanism for heterogeneous catalysis related to the selectivity in the cyclization process is presented herein. Solketal, a commercial product, was also obtained by a condensation reaction of glycerol and propanone, and showed a high selectivity in favor of 1,3-dioxolane. It was transformed to potential allylic and chiral intermediates. A mesogenic core was connected to the organic framework of glycerol to produce a monomer liquid crystal material with a stable smectic-C mesophase.application/pdfporQuímica nova. São Paulo. Vol. 38, n. 8 (set. 2015), p. 1053-1062GlicerolCondensaçãoCompostos carbonílicosCristais líquidosGlycerol derivativesCondensation reactionHeterogeneous catalystLiquid crystalsSolketal transformationReação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidosCondensation reaction of glycerol and carbonyl compounds : synthesis, characterization, and derivatization for liquid crystalsinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000980570.pdf000980570.pdfTexto completoapplication/pdf1676195http://www.lume.ufrgs.br/bitstream/10183/131116/1/000980570.pdfa3b44ac067d1829d3c2439caf609ac75MD51TEXT000980570.pdf.txt000980570.pdf.txtExtracted Texttext/plain47888http://www.lume.ufrgs.br/bitstream/10183/131116/2/000980570.pdf.txte02018e11538b9181978cc445f686788MD52THUMBNAIL000980570.pdf.jpg000980570.pdf.jpgGenerated Thumbnailimage/jpeg1931http://www.lume.ufrgs.br/bitstream/10183/131116/3/000980570.pdf.jpg9672ac556ffdbe9de2ab74aa453308ffMD5310183/1311162018-10-25 09:49:08.721oai:www.lume.ufrgs.br:10183/131116Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-10-25T12:49:08Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
dc.title.alternative.en.fl_str_mv Condensation reaction of glycerol and carbonyl compounds : synthesis, characterization, and derivatization for liquid crystals
title Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
spellingShingle Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
Kautz, Jacqueline
Glicerol
Condensação
Compostos carbonílicos
Cristais líquidos
Glycerol derivatives
Condensation reaction
Heterogeneous catalyst
Liquid crystals
Solketal transformation
title_short Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
title_full Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
title_fullStr Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
title_full_unstemmed Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
title_sort Reação de condensação do glicerol com compostos carbonílicos : síntese, caracterização e aplicação em cristais líquidos
author Kautz, Jacqueline
author_facet Kautz, Jacqueline
Feltrin, Carlos Willian
Sales, Eric Souza
Eifler-Lima, Vera Lucia
Merlo, Aloir Antonio
author_role author
author2 Feltrin, Carlos Willian
Sales, Eric Souza
Eifler-Lima, Vera Lucia
Merlo, Aloir Antonio
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Kautz, Jacqueline
Feltrin, Carlos Willian
Sales, Eric Souza
Eifler-Lima, Vera Lucia
Merlo, Aloir Antonio
dc.subject.por.fl_str_mv Glicerol
Condensação
Compostos carbonílicos
Cristais líquidos
topic Glicerol
Condensação
Compostos carbonílicos
Cristais líquidos
Glycerol derivatives
Condensation reaction
Heterogeneous catalyst
Liquid crystals
Solketal transformation
dc.subject.eng.fl_str_mv Glycerol derivatives
Condensation reaction
Heterogeneous catalyst
Liquid crystals
Solketal transformation
description Condensation reactions of glycerol with aldehydes and ketones were performed under thermal heating and microwave irradiation regimes. Homogeneous and heterogeneous catalysts were tested in both conditions. A silica sulfated (SiO2–SO3H) heterogeneous catalyst demonstrated the best performance relative to a selectivity of >95% in favor of 5-membered ketals. For acetals, preference in favor of 5-membered or 6-membered functional groups depends on the nature of the catalyst. Homogenous catalysts favor the more stable 6-membered acetals, whereas heterogeneous catalysts favor the less stable 5-membered acetals. However, the isomer ratios in the acetalization reaction are too low, and hence the reaction cannot be used in a synthetic plan for functional materials. Ketalization processes mediated by SiO2–SO3H show a high selectivity in favor of a 5-membered ring (1,3-dioxolane). The scope of condensation was tested with different ketones. A mechanism for heterogeneous catalysis related to the selectivity in the cyclization process is presented herein. Solketal, a commercial product, was also obtained by a condensation reaction of glycerol and propanone, and showed a high selectivity in favor of 1,3-dioxolane. It was transformed to potential allylic and chiral intermediates. A mesogenic core was connected to the organic framework of glycerol to produce a monomer liquid crystal material with a stable smectic-C mesophase.
publishDate 2015
dc.date.accessioned.fl_str_mv 2015-12-15T02:37:47Z
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dc.relation.ispartof.pt_BR.fl_str_mv Química nova. São Paulo. Vol. 38, n. 8 (set. 2015), p. 1053-1062
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