Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo
| Ano de defesa: | 2017 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | |
| Tipo de documento: | Dissertação |
| Tipo de acesso: | Acesso aberto |
| Idioma: | por |
| Instituição de defesa: |
Universidade Federal da Paraíba
|
| 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: | https://repositorio.ufpb.br/jspui/handle/tede/9185 |
Resumo: | This work reports the synthesis, characterization and investigation of the luminescent properties of new lanthanide -diketonate complexes, Ln(- dic)2(NO3)L2, Ln(TTA)3L2 and Ln(DBM)3L (TPPO), where thenoyltrifluoroacetone (TTA) and dibenzoylmethane (DBM), L = triphenylphosphine oxide (TPPO), tributylphosphine oxide (TBPO), and trioctylphosphine oxide (TOPO). Eu3+ ion complexes were also synthesized with triphenylarsine oxide (TPAsO) and tricyclohexylphosphine (TCHPO) as auxiliary ligands. The complexes were characterized by complexometric titration with EDTA, CHN elemental analysis, Fourier transform infrared (FTIR) absorption spectroscopy and thermogravimetric analysis (TGA). The photoluminescent properties in the visible and near infrared (NIR) regions of the synthesized complexes were investigated from excitation, emission and luminescence decay curves. The excitation spectra are characterized by the presence of large bands associated with transitions centered on the ligands, evidencing the efficiency of the luminescence sensitization by the antenna ligands. The emission spectra in the visible region of the compounds of the Sm3+ and Eu3+ ions show narrow bands attributed to intraconfigurationtransitions and are dominated by the hypersensitive transitions (~645 nm) and (~612 nm). The values of the intensity parameters and for the complexes of Sm3+ and Eu3+ presented a good correlation, evidencing that the chemical environment influence in a similar way the spectroscopic properties of these ions. The photoluminescent properties of the Eu3+ ion complexes were investigated by the intensity parameters and , radiative and nonradiative ( and ), lifetime of the emitting state () and quantum emission efficience . The highest values of are found for Eu(-dic)2(NO3)L2 complexes, in the range of 51-86%. It was observed that the Eu(-dic)3L2 compounds exhibited shorter lifetimes, which may be related to the presence of a suppressor channel, resulting in higher values of . The intensity parameters and vary only slightly when changes occur in the number and nature of the ligands of the first coordination sphere, with parameter being more sensitive to changes in coordination geometry. The emission spectra in the NIR region of the bis- and trisdiketonate complexes of Pr3+, Nd3+, Sm3+, Er3+ and Yb3+ ions present characteristic luminescence. Changes in the nature and number of ligands coordinated to the Ln3+ ion slightly influence the spectral profiles. The results obtained for the studied systems suggest that these are potential candidates to act as Molecular Light Converting Devices. |
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2017-07-31T14:45:43Z2018-07-21T00:30:14Z2018-07-21T00:30:14Z2017-02-13MOURA. Jandeilson de Lima. Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo. 2017. 159 f. Dissertação (Mestrado em Química)- Universidade Federal da Paraíba, João Pessoa, 2017.https://repositorio.ufpb.br/jspui/handle/tede/9185This work reports the synthesis, characterization and investigation of the luminescent properties of new lanthanide -diketonate complexes, Ln(- dic)2(NO3)L2, Ln(TTA)3L2 and Ln(DBM)3L (TPPO), where thenoyltrifluoroacetone (TTA) and dibenzoylmethane (DBM), L = triphenylphosphine oxide (TPPO), tributylphosphine oxide (TBPO), and trioctylphosphine oxide (TOPO). Eu3+ ion complexes were also synthesized with triphenylarsine oxide (TPAsO) and tricyclohexylphosphine (TCHPO) as auxiliary ligands. The complexes were characterized by complexometric titration with EDTA, CHN elemental analysis, Fourier transform infrared (FTIR) absorption spectroscopy and thermogravimetric analysis (TGA). The photoluminescent properties in the visible and near infrared (NIR) regions of the synthesized complexes were investigated from excitation, emission and luminescence decay curves. The excitation spectra are characterized by the presence of large bands associated with transitions centered on the ligands, evidencing the efficiency of the luminescence sensitization by the antenna ligands. The emission spectra in the visible region of the compounds of the Sm3+ and Eu3+ ions show narrow bands attributed to intraconfigurationtransitions and are dominated by the hypersensitive transitions (~645 nm) and (~612 nm). The values of the intensity parameters and for the complexes of Sm3+ and Eu3+ presented a good correlation, evidencing that the chemical environment influence in a similar way the spectroscopic properties of these ions. The photoluminescent properties of the Eu3+ ion complexes were investigated by the intensity parameters and , radiative and nonradiative ( and ), lifetime of the emitting state () and quantum emission efficience . The highest values of are found for Eu(-dic)2(NO3)L2 complexes, in the range of 51-86%. It was observed that the Eu(-dic)3L2 compounds exhibited shorter lifetimes, which may be related to the presence of a suppressor channel, resulting in higher values of . The intensity parameters and vary only slightly when changes occur in the number and nature of the ligands of the first coordination sphere, with parameter being more sensitive to changes in coordination geometry. The emission spectra in the NIR region of the bis- and trisdiketonate complexes of Pr3+, Nd3+, Sm3+, Er3+ and Yb3+ ions present characteristic luminescence. Changes in the nature and number of ligands coordinated to the Ln3+ ion slightly influence the spectral profiles. The results obtained for the studied systems suggest that these are potential candidates to act as Molecular Light Converting Devices.Este trabalho reporta a síntese, caracterização e investigação das propriedades luminescentes de -dicetonatos de íons lantanídos, Ln(- dic)2(NO3)L2, Ln(TTA)3L2 e Ln(DBM)3L, em que Ln3+ = Pr3+, Nd3+, Sm3+, Eu3+, Er3+ e Yb3+, -dic = 2-tenoilltrifluoroacetona (TTA) e dibenzoilmetano (DBM), L = óxido de trifenilfosfina (TPPO), tributilfosfina (TBPO) e trioctilfosfina (TOPO). Para os compostos do íon Eu3+, foram também sintetizados os complexos com o óxido de trifenilarsina (TPAsO) e triciclohexilfosfina (TCHPO) como ligantes auxiliares. Os complexos sintetizados foram caracterizados por titulação complexométrica com EDTA, análise elementar CHN, espectroscopia de absorção na região do infravermelho com transformada de Fourier (FTIR) e análise termogravimétrica (TGA). As propriedades fotoluminescentes nas regiões do visível e infravermelho próximo (NIR) dos complexos sintetizados foram investigadas a partir dos espectros de excitação, emissão e curvas de decaimento de luminescência. Os espectros de excitação são caracterizados pela presença de bandas largas associadas às transições centradas nos ligantes , evidenciando a eficiência na sensibilização da luminescência pelos ligantes antenas. Os espectros de emissão, na região do visível, dos compostos dos íons Sm3+ e Eu3+, exibem bandas finas oriundas das transições intraconfiguracionaise são dominados pelas transições hipersensíveis (~645 nm) e (~612 nm). Os valores dos parâmetros de intensidade e dos complexos de Sm3+ e Eu3+ apresentaram uma boa correlação, evidenciando que o ambiente químico influência de maneira semelhante as propriedades espectroscópica destes íons. As propriedades fotoluminescentes dos complexos do íon Eu3+ foram investigados por meio dos parâmetros de intensidade e , taxas de radiativa e nãoradiativa ( e ), tempo de vida do estado () e, eficiência quântica de emissão ( ). Os maiores valores de são encontrados para os complexos Eu(- dic)2(NO3)L2, na faixa de 51-86%. Observou-se que os compostos Eu(-dic)3L2 exibiram tempo de vida mais curto, o que pode estar relacionado com a presença de uma canal supressor, resultando assim em maiores valores de . Os parâmetros de intensidade e , variam apenas ligeiramente quando ocorre alterações no número e na natureza dos ligantes da primeira esfera de coordenação, sendo o 2 mais sensível as alterações na geometria de coordenação. Os espectros de emissão na região do NIR dos complexos bis- e tris-dicetonatos dos íons Pr3+, Nd3+, Sm3+, Er3+ e Yb3+ apresentam luminescência característica. As alterações na natureza e número de ligantes coordenados ao íon Ln3+ influenciam ligeiramente os perfis espectrais. Os resultados obtidos para os sistemas estudados sugerem que estes são potenciais candidatos a atuarem como Dispositivos Moleculares Conversores de Luz.Submitted by ANA KARLA PEREIRA RODRIGUES (anakarla_@hotmail.com) on 2017-07-31T14:45:43Z No. of bitstreams: 1 arquivototal.pdf: 9976488 bytes, checksum: d0e80f609f413107e918fa94fe016bad (MD5)Made available in DSpace on 2017-07-31T14:45:43Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 9976488 bytes, checksum: d0e80f609f413107e918fa94fe016bad (MD5) Previous issue date: 2017-02-13Made available in DSpace on 2018-07-21T00:30:14Z (GMT). No. of bitstreams: 3 arquivototal.pdf: 9976488 bytes, checksum: d0e80f609f413107e918fa94fe016bad (MD5) arquivototal.pdf.txt: 159112 bytes, checksum: db3f66241cddb6aa42bf66305229db75 (MD5) arquivototal.pdf.jpg: 4930 bytes, checksum: 97bfc546587381a26e6da2f781eb5a16 (MD5) Previous issue date: 2017-02-13Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqapplication/pdfporUniversidade Federal da ParaíbaPrograma de Pós-Graduação em QuímicaUFPBBrasilQuímicaLantanídeosLuminescência no Infravermelho PróximoTransferência de energia.LanthanidesNear Infrared LuminescenceEnergy transferCIENCIAS EXATAS E DA TERRA::QUIMICAEstudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximoinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisTeotonio, Ercules Epaminondas de Sousa97789704400http://lattes.cnpq.br/804209263120700409438881409http://lattes.cnpq.br/5406003013456173Moura, Jandeilson de Limahttps://repositorio.ufpb.br/jspui/retrieve/18614/arquivototal.pdf.jpginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFPBinstname:Universidade Federal da Paraíba (UFPB)instacron:UFPBTHUMBNAILarquivototal.pdf.jpgarquivototal.pdf.jpgIM Thumbnailimage/jpeg4031https://repositorio.ufpb.br/jspui/bitstream/tede/9185/7/arquivototal.pdf.jpgb4a9f1a3560b14f1dd9ba71601dbcf35MD57TEXTarquivototal.pdf.txtarquivototal.pdf.txtExtracted texttext/plain164351https://repositorio.ufpb.br/jspui/bitstream/tede/9185/6/arquivototal.pdf.txt67ffdb1342dd4ae3c0892e0a3059d82aMD56ORIGINALarquivototal.pdfarquivototal.pdfArquivo Totalapplication/pdf9976488https://repositorio.ufpb.br/jspui/bitstream/tede/9185/2/arquivototal.pdfd0e80f609f413107e918fa94fe016badMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81892https://repositorio.ufpb.br/jspui/bitstream/tede/9185/1/license.txt8c8cacc7fa454d1f71e17b728b8bcecdMD51license.txtlicense.txttext/plain; charset=utf-81867https://repositorio.ufpb.br/jspui/bitstream/tede/9185/5/license.txt07956d2f9f6879bad6c75289be248398MD55tede/91852018-09-05 23:13:36.342oai:repositorio.ufpb.br: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Repositório InstitucionalPUBhttps://repositorio.ufpb.br/oai/requestdiretoria@ufpb.br||bdtd@biblioteca.ufpb.bropendoar:25462018-09-06T02:13:36Repositório Institucional da UFPB - Universidade Federal da Paraíba (UFPB)false |
| dc.title.por.fl_str_mv |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo |
| title |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo |
| spellingShingle |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo Moura, Jandeilson de Lima Lantanídeos Luminescência no Infravermelho Próximo Transferência de energia. Lanthanides Near Infrared Luminescence Energy transfer CIENCIAS EXATAS E DA TERRA::QUIMICA |
| title_short |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo |
| title_full |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo |
| title_fullStr |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo |
| title_full_unstemmed |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo |
| title_sort |
Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo |
| author |
Moura, Jandeilson de Lima |
| author_facet |
Moura, Jandeilson de Lima |
| author_role |
author |
| dc.contributor.advisor1.fl_str_mv |
Teotonio, Ercules Epaminondas de Sousa |
| dc.contributor.advisor1ID.fl_str_mv |
97789704400 |
| dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/8042092631207004 |
| dc.contributor.authorID.fl_str_mv |
09438881409 |
| dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/5406003013456173 |
| dc.contributor.author.fl_str_mv |
Moura, Jandeilson de Lima |
| contributor_str_mv |
Teotonio, Ercules Epaminondas de Sousa |
| dc.subject.por.fl_str_mv |
Lantanídeos Luminescência no Infravermelho Próximo Transferência de energia. |
| topic |
Lantanídeos Luminescência no Infravermelho Próximo Transferência de energia. Lanthanides Near Infrared Luminescence Energy transfer CIENCIAS EXATAS E DA TERRA::QUIMICA |
| dc.subject.eng.fl_str_mv |
Lanthanides Near Infrared Luminescence Energy transfer |
| dc.subject.cnpq.fl_str_mv |
CIENCIAS EXATAS E DA TERRA::QUIMICA |
| description |
This work reports the synthesis, characterization and investigation of the luminescent properties of new lanthanide -diketonate complexes, Ln(- dic)2(NO3)L2, Ln(TTA)3L2 and Ln(DBM)3L (TPPO), where thenoyltrifluoroacetone (TTA) and dibenzoylmethane (DBM), L = triphenylphosphine oxide (TPPO), tributylphosphine oxide (TBPO), and trioctylphosphine oxide (TOPO). Eu3+ ion complexes were also synthesized with triphenylarsine oxide (TPAsO) and tricyclohexylphosphine (TCHPO) as auxiliary ligands. The complexes were characterized by complexometric titration with EDTA, CHN elemental analysis, Fourier transform infrared (FTIR) absorption spectroscopy and thermogravimetric analysis (TGA). The photoluminescent properties in the visible and near infrared (NIR) regions of the synthesized complexes were investigated from excitation, emission and luminescence decay curves. The excitation spectra are characterized by the presence of large bands associated with transitions centered on the ligands, evidencing the efficiency of the luminescence sensitization by the antenna ligands. The emission spectra in the visible region of the compounds of the Sm3+ and Eu3+ ions show narrow bands attributed to intraconfigurationtransitions and are dominated by the hypersensitive transitions (~645 nm) and (~612 nm). The values of the intensity parameters and for the complexes of Sm3+ and Eu3+ presented a good correlation, evidencing that the chemical environment influence in a similar way the spectroscopic properties of these ions. The photoluminescent properties of the Eu3+ ion complexes were investigated by the intensity parameters and , radiative and nonradiative ( and ), lifetime of the emitting state () and quantum emission efficience . The highest values of are found for Eu(-dic)2(NO3)L2 complexes, in the range of 51-86%. It was observed that the Eu(-dic)3L2 compounds exhibited shorter lifetimes, which may be related to the presence of a suppressor channel, resulting in higher values of . The intensity parameters and vary only slightly when changes occur in the number and nature of the ligands of the first coordination sphere, with parameter being more sensitive to changes in coordination geometry. The emission spectra in the NIR region of the bis- and trisdiketonate complexes of Pr3+, Nd3+, Sm3+, Er3+ and Yb3+ ions present characteristic luminescence. Changes in the nature and number of ligands coordinated to the Ln3+ ion slightly influence the spectral profiles. The results obtained for the studied systems suggest that these are potential candidates to act as Molecular Light Converting Devices. |
| publishDate |
2017 |
| dc.date.accessioned.fl_str_mv |
2017-07-31T14:45:43Z 2018-07-21T00:30:14Z |
| dc.date.issued.fl_str_mv |
2017-02-13 |
| dc.date.available.fl_str_mv |
2018-07-21T00:30:14Z |
| dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
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masterThesis |
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publishedVersion |
| dc.identifier.citation.fl_str_mv |
MOURA. Jandeilson de Lima. Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo. 2017. 159 f. Dissertação (Mestrado em Química)- Universidade Federal da Paraíba, João Pessoa, 2017. |
| dc.identifier.uri.fl_str_mv |
https://repositorio.ufpb.br/jspui/handle/tede/9185 |
| identifier_str_mv |
MOURA. Jandeilson de Lima. Estudos espectroscópicos de novos complexos B-dicetonatos de íons lantanídeos com emissão no visível e infravermelho próximo. 2017. 159 f. Dissertação (Mestrado em Química)- Universidade Federal da Paraíba, João Pessoa, 2017. |
| url |
https://repositorio.ufpb.br/jspui/handle/tede/9185 |
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por |
| language |
por |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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Universidade Federal da Paraíba |
| dc.publisher.program.fl_str_mv |
Programa de Pós-Graduação em Química |
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UFPB |
| dc.publisher.country.fl_str_mv |
Brasil |
| dc.publisher.department.fl_str_mv |
Química |
| publisher.none.fl_str_mv |
Universidade Federal da Paraíba |
| dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFPB instname:Universidade Federal da Paraíba (UFPB) instacron:UFPB |
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Universidade Federal da Paraíba (UFPB) |
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UFPB |
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UFPB |
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Repositório Institucional da UFPB |
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Repositório Institucional da UFPB - Universidade Federal da Paraíba (UFPB) |
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diretoria@ufpb.br||bdtd@biblioteca.ufpb.br |
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