Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)

Detalhes bibliográficos
Ano de defesa: 2017
Autor(a) principal: Rodrigues, Jéssica Fonseca lattes
Orientador(a): Lang, Ernesto Schulz lattes
Banca de defesa: Stieler, Rafael lattes, Schumacher, Ricardo Frederico lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Química
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/14091
Resumo: This work describes the synthesis and structural characterization of new organochalcogenoxanes polymer and clusters compounds containing yttrium(III) ion. The synthetized compounds have structure of unidimensional coordination polymer [Y(C6H5SeO2)2(NO3)(CH3OH)]n (1) which grows along crystallographic axis a and macromolecular clusters [(C6H5Te)18O24{Y(NO3)(H2O)}216+] (2), [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)2}212+] (3) and [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)3}210+] (4). There is a lack of study of compounds containing organocalcogenoxanes (R-E-O, where R = aryl, E = Se, Te) and its known that they compose a great variety of compounds of interesting morphologies. So, knowing that yttrium(III) ion is one of the hardest species according to Pearson’s Theory, this property was utilized to synthetize compounds where this ion coordinates to oxygen, the hard atom of organocalcogenoxanes ligands. From the reaction of phenylseleninic acid with yttrium(III) salt, a coordination polymer was synthetized (1) and the versatility of coordination modes of this ligand can be observed. In the synthesis of compounds 2, 3 and 4, phenyltellurium(IV) triiodide was utilized, which doesn’t contain any oxygen originally, but suffer an in situ hydrolysis reaction producing phenyltellurinic acid. Due to the hypervalent character of the tellurium atom, half-spheres were formed interconnected by iodine rings in (2) or phenylseleninate bridges in (3) and (4). Yttrium(III) plays an important role in the formation of this clusters because it acts as a template, confirmed due the attempt to perform the same reaction without the presence of this ion, and the impossibility to get the same compounds. The compounds were characterized by X-ray diffraction, infrared spectroscopy, elemental analysis and mass spectrometry.
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spelling 2018-08-23T20:38:03Z2018-08-23T20:38:03Z2017-07-26http://repositorio.ufsm.br/handle/1/14091This work describes the synthesis and structural characterization of new organochalcogenoxanes polymer and clusters compounds containing yttrium(III) ion. The synthetized compounds have structure of unidimensional coordination polymer [Y(C6H5SeO2)2(NO3)(CH3OH)]n (1) which grows along crystallographic axis a and macromolecular clusters [(C6H5Te)18O24{Y(NO3)(H2O)}216+] (2), [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)2}212+] (3) and [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)3}210+] (4). There is a lack of study of compounds containing organocalcogenoxanes (R-E-O, where R = aryl, E = Se, Te) and its known that they compose a great variety of compounds of interesting morphologies. So, knowing that yttrium(III) ion is one of the hardest species according to Pearson’s Theory, this property was utilized to synthetize compounds where this ion coordinates to oxygen, the hard atom of organocalcogenoxanes ligands. From the reaction of phenylseleninic acid with yttrium(III) salt, a coordination polymer was synthetized (1) and the versatility of coordination modes of this ligand can be observed. In the synthesis of compounds 2, 3 and 4, phenyltellurium(IV) triiodide was utilized, which doesn’t contain any oxygen originally, but suffer an in situ hydrolysis reaction producing phenyltellurinic acid. Due to the hypervalent character of the tellurium atom, half-spheres were formed interconnected by iodine rings in (2) or phenylseleninate bridges in (3) and (4). Yttrium(III) plays an important role in the formation of this clusters because it acts as a template, confirmed due the attempt to perform the same reaction without the presence of this ion, and the impossibility to get the same compounds. The compounds were characterized by X-ray diffraction, infrared spectroscopy, elemental analysis and mass spectrometry.O presente trabalho descreve a síntese e caracterização estrutural de novos compostos poliméricos e clusters derivados de organocalcogenoxanos contendo o íon ítrio(III). Os compostos sintetizados estão na forma do polímero de coordenação unidimensional [Y(C6H5SeO2)2(NO3)(CH3OH)]n (1), o qual cresce ao longo do eixo cristalográfico a, e clusters polinucleares macromoleculares [(C6H5Te)18O24{Y(NO3)(H2O)}216+] (2), [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)2}212+] (3) e [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)3}210+] (4). O estudo de compostos contendo organocalcogenoxanos (R-E-O, onde R = arila, E = Se, Te) é escasso e sabe-se que o uso dos mesmos compõe uma classe de grande variedade estrutural e morfologias interessantes. Sendo assim, sabendo-se que o íon ítrio(III) é uma das espécies de maior caráter duro de acordo com a Teoria de Pearson, utilizou-se esta propriedade para sintetizar compostos onde o ítrio(III) se coordena ao oxigênio, centro duro de ligantes derivados de organocalcogenoxanos. A partir da reação do ácido fenilselenínico com o sal de ítrio(III), obteve-se o complexo polimérico (1), no qual se pode observar a versatilidade deste ligante quanto aos seus modos de coordenação. Na síntese dos compostos (2, 3 e 4), utilizou-se triiodeto de feniltelúrio, o qual não contém originalmente oxigênio em sua composição, mas sofre uma reação de hidrólise in situ, formando o ácido feniltelurínico. Devido ao maior caráter metálico e maior raio atômico do telúrio, formam-se meia esferas interligadas por anéis de iodo em 2 ou fenilseleninatos em 3 e 4. O ítrio(III) possui papel fundamental na formação dos clusters pois atua como template, o que pode ser confirmado devido à tentativa de realizar a mesma reação sem a presença deste íon, não sendo possível obter os mesmos compostos. Os compostos obtidos foram caracterizados por difração de raios X em monocristal, espectroscopia na região do infravermelho, análise elementar e espectrometria de massas.Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqporUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em QuímicaUFSMBrasilQuímicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessOrganocalcogenoxanosÍtrio(III)Polímero de coordenaçãoCluster macromolecularOrganochalcogenoxanesYttrium(III)Coordination polymerMacromolecular clusterCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICASíntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)Synthesis and structural characterization of new organochalcogenoxanes compounds containing yttrium(III)info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisLang, Ernesto Schulzhttp://lattes.cnpq.br/4481982189769819Stieler, Rafaelhttp://lattes.cnpq.br/6824260536594075Schumacher, Ricardo Fredericohttp://lattes.cnpq.br/7856034546434135http://lattes.cnpq.br/7793853870530762Rodrigues, Jéssica Fonseca1006000000006000c9d7568-d5c4-466d-b807-0125a7d37b975d0c00dc-a90f-49b2-85ab-243052b42d704e2eba6e-3462-4f5f-85b0-3cb2ae5c69d56a26f817-0d52-41d8-9183-c785c92d110areponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGQUIMICA_2017_RODRIGUES_JESSICA.pdfDIS_PPGQUIMICA_2017_RODRIGUES_JESSICA.pdfDissertação de Mestradoapplication/pdf4595562http://repositorio.ufsm.br/bitstream/1/14091/1/DIS_PPGQUIMICA_2017_RODRIGUES_JESSICA.pdf1bc78c02aeae483d5f04d4deb6f80913MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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dc.title.por.fl_str_mv Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
dc.title.alternative.eng.fl_str_mv Synthesis and structural characterization of new organochalcogenoxanes compounds containing yttrium(III)
title Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
spellingShingle Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
Rodrigues, Jéssica Fonseca
Organocalcogenoxanos
Ítrio(III)
Polímero de coordenação
Cluster macromolecular
Organochalcogenoxanes
Yttrium(III)
Coordination polymer
Macromolecular cluster
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
title_full Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
title_fullStr Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
title_full_unstemmed Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
title_sort Síntese e caracterização estrutural de novos compostos organocalcogenoxanos contendo ítrio(III)
author Rodrigues, Jéssica Fonseca
author_facet Rodrigues, Jéssica Fonseca
author_role author
dc.contributor.advisor1.fl_str_mv Lang, Ernesto Schulz
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/4481982189769819
dc.contributor.referee1.fl_str_mv Stieler, Rafael
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/6824260536594075
dc.contributor.referee2.fl_str_mv Schumacher, Ricardo Frederico
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/7856034546434135
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/7793853870530762
dc.contributor.author.fl_str_mv Rodrigues, Jéssica Fonseca
contributor_str_mv Lang, Ernesto Schulz
Stieler, Rafael
Schumacher, Ricardo Frederico
dc.subject.por.fl_str_mv Organocalcogenoxanos
Ítrio(III)
Polímero de coordenação
Cluster macromolecular
topic Organocalcogenoxanos
Ítrio(III)
Polímero de coordenação
Cluster macromolecular
Organochalcogenoxanes
Yttrium(III)
Coordination polymer
Macromolecular cluster
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Organochalcogenoxanes
Yttrium(III)
Coordination polymer
Macromolecular cluster
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description This work describes the synthesis and structural characterization of new organochalcogenoxanes polymer and clusters compounds containing yttrium(III) ion. The synthetized compounds have structure of unidimensional coordination polymer [Y(C6H5SeO2)2(NO3)(CH3OH)]n (1) which grows along crystallographic axis a and macromolecular clusters [(C6H5Te)18O24{Y(NO3)(H2O)}216+] (2), [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)2}212+] (3) and [{(C6H5Te)18O24Y(NO3)(H2O)(C6H5SeO2)3}210+] (4). There is a lack of study of compounds containing organocalcogenoxanes (R-E-O, where R = aryl, E = Se, Te) and its known that they compose a great variety of compounds of interesting morphologies. So, knowing that yttrium(III) ion is one of the hardest species according to Pearson’s Theory, this property was utilized to synthetize compounds where this ion coordinates to oxygen, the hard atom of organocalcogenoxanes ligands. From the reaction of phenylseleninic acid with yttrium(III) salt, a coordination polymer was synthetized (1) and the versatility of coordination modes of this ligand can be observed. In the synthesis of compounds 2, 3 and 4, phenyltellurium(IV) triiodide was utilized, which doesn’t contain any oxygen originally, but suffer an in situ hydrolysis reaction producing phenyltellurinic acid. Due to the hypervalent character of the tellurium atom, half-spheres were formed interconnected by iodine rings in (2) or phenylseleninate bridges in (3) and (4). Yttrium(III) plays an important role in the formation of this clusters because it acts as a template, confirmed due the attempt to perform the same reaction without the presence of this ion, and the impossibility to get the same compounds. The compounds were characterized by X-ray diffraction, infrared spectroscopy, elemental analysis and mass spectrometry.
publishDate 2017
dc.date.issued.fl_str_mv 2017-07-26
dc.date.accessioned.fl_str_mv 2018-08-23T20:38:03Z
dc.date.available.fl_str_mv 2018-08-23T20:38:03Z
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 http://repositorio.ufsm.br/handle/1/14091
url http://repositorio.ufsm.br/handle/1/14091
dc.language.iso.fl_str_mv por
language por
dc.relation.cnpq.fl_str_mv 100600000000
dc.relation.confidence.fl_str_mv 600
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dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química
dc.publisher.initials.fl_str_mv UFSM
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Química
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações do UFSM
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