Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides

Detalhes bibliográficos
Autor(a) principal: Sousa, Filipa L.
Data de Publicação: 2006
Outros Autores: Pillinger, Martyn, Ferreira, Rute A. Sá, Granadeiro, Carlos M., Cavaleiro, Ana M. V., Rocha, João, Carlos, Luís D., Trindade, Tito, Nogueira, Helena I. S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/5716
Resumo: Novel luminescent polyoxometalate anion-pillared layered double hydroxides (LDHs) were prepared by aqueous ion exchange of a Zn–Al LDH precursor in nitrate form with the europium-containing polyoxotungstate anions [EuW10O36]9–, [Eu(BW11O39)(H2O)3]6– and [Eu(PW11O39)2]11–. The host– guest interaction has a strong influence on the nature of the final intercalated species, as evidenced by elemental analy- Introduction Layered double hydroxides are an important class of ionic lamellar solids with the general formula [M2+ 1–xM3+ x(OH)2](Am–)x/m·nH2O (M2+ = Mg2+, Zn2+, Ni2+ etc., M3+ = Al3+, Cr3+, Ga3+ etc).[1] The positively charged layers, containing divalent and trivalent cations in octahedral positions, are separated by charge balancing anions and water molecules. The water molecules are connected to both the metal hydroxide layers and the interlayer anions through extensive hydrogen bonding. A range of organic or inorganic guests may be incorporated into LDHs by either ion exchange, direct synthesis or hydrothermal reconstruction of calcined precursors.[2,3] In particular, intercalation chemistry has been explored with the aim of introducing catalytically active sites and photo- and electroactive species. Many different types of metal coordination compounds and oxometalates have been immobilized in LDHs, including phthalocyanines, cyanocomplexes, oxalate complexes and polyoxometalates (POMs).[4] The first report of LDHs containing polyoxometalates concerned their use as exhaust gas and hydrocarbon conversion catalysts.[5] Since then, a variety of iso- and heteropolyanions with different nuclearities and structures (Keggin, Dawson, Preyssler, Finke) have been incorporated into the interlayer space of these materials.[6–18] Two factors assume considerable importance for the successful intercalation of polyoxometalates into an LDH compound. First, the heteropoly species should carry sufficient charge in order to be [a] Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal E-mail: helena@dq.ua.pt [b] Department of Physics, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal © 2006 Wiley-VCH Verlag 726 GmbH & Co. KGaA, Weinheim Eur. J. Inorg. Chem. 2006, 726–734 sis, powder X-ray diffraction (XRD), infra-red (IR) and Raman spectroscopy, solid state magic-angle spinning (MAS) 11B and 31P NMR spectroscopy, and photoluminescence spectroscopy.
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spelling Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxidesLayered double hydroxidesLayered compoundsPolyoxometalatesHost–guest systemsLuminescenceNovel luminescent polyoxometalate anion-pillared layered double hydroxides (LDHs) were prepared by aqueous ion exchange of a Zn–Al LDH precursor in nitrate form with the europium-containing polyoxotungstate anions [EuW10O36]9–, [Eu(BW11O39)(H2O)3]6– and [Eu(PW11O39)2]11–. The host– guest interaction has a strong influence on the nature of the final intercalated species, as evidenced by elemental analy- Introduction Layered double hydroxides are an important class of ionic lamellar solids with the general formula [M2+ 1–xM3+ x(OH)2](Am–)x/m·nH2O (M2+ = Mg2+, Zn2+, Ni2+ etc., M3+ = Al3+, Cr3+, Ga3+ etc).[1] The positively charged layers, containing divalent and trivalent cations in octahedral positions, are separated by charge balancing anions and water molecules. The water molecules are connected to both the metal hydroxide layers and the interlayer anions through extensive hydrogen bonding. A range of organic or inorganic guests may be incorporated into LDHs by either ion exchange, direct synthesis or hydrothermal reconstruction of calcined precursors.[2,3] In particular, intercalation chemistry has been explored with the aim of introducing catalytically active sites and photo- and electroactive species. Many different types of metal coordination compounds and oxometalates have been immobilized in LDHs, including phthalocyanines, cyanocomplexes, oxalate complexes and polyoxometalates (POMs).[4] The first report of LDHs containing polyoxometalates concerned their use as exhaust gas and hydrocarbon conversion catalysts.[5] Since then, a variety of iso- and heteropolyanions with different nuclearities and structures (Keggin, Dawson, Preyssler, Finke) have been incorporated into the interlayer space of these materials.[6–18] Two factors assume considerable importance for the successful intercalation of polyoxometalates into an LDH compound. First, the heteropoly species should carry sufficient charge in order to be [a] Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal E-mail: helena@dq.ua.pt [b] Department of Physics, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal © 2006 Wiley-VCH Verlag 726 GmbH & Co. KGaA, Weinheim Eur. J. Inorg. Chem. 2006, 726–734 sis, powder X-ray diffraction (XRD), infra-red (IR) and Raman spectroscopy, solid state magic-angle spinning (MAS) 11B and 31P NMR spectroscopy, and photoluminescence spectroscopy.WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim2006-022006-02-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/5716eng1434-1948Sousa, Filipa L.Pillinger, MartynFerreira, Rute A. SáGranadeiro, Carlos M.Cavaleiro, Ana M. V.Rocha, JoãoCarlos, Luís D.Trindade, TitoNogueira, Helena I. S.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-17T03:22:28ZPortal AgregadorONG
dc.title.none.fl_str_mv Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
title Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
spellingShingle Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
Sousa, Filipa L.
Layered double hydroxides
Layered compounds
Polyoxometalates
Host–guest systems
Luminescence
title_short Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
title_full Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
title_fullStr Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
title_full_unstemmed Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
title_sort Luminescent polyoxotungstoeuropate anion-pillared layered double hydroxides
author Sousa, Filipa L.
author_facet Sousa, Filipa L.
Pillinger, Martyn
Ferreira, Rute A. Sá
Granadeiro, Carlos M.
Cavaleiro, Ana M. V.
Rocha, João
Carlos, Luís D.
Trindade, Tito
Nogueira, Helena I. S.
author_role author
author2 Pillinger, Martyn
Ferreira, Rute A. Sá
Granadeiro, Carlos M.
Cavaleiro, Ana M. V.
Rocha, João
Carlos, Luís D.
Trindade, Tito
Nogueira, Helena I. S.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sousa, Filipa L.
Pillinger, Martyn
Ferreira, Rute A. Sá
Granadeiro, Carlos M.
Cavaleiro, Ana M. V.
Rocha, João
Carlos, Luís D.
Trindade, Tito
Nogueira, Helena I. S.
dc.subject.por.fl_str_mv Layered double hydroxides
Layered compounds
Polyoxometalates
Host–guest systems
Luminescence
topic Layered double hydroxides
Layered compounds
Polyoxometalates
Host–guest systems
Luminescence
description Novel luminescent polyoxometalate anion-pillared layered double hydroxides (LDHs) were prepared by aqueous ion exchange of a Zn–Al LDH precursor in nitrate form with the europium-containing polyoxotungstate anions [EuW10O36]9–, [Eu(BW11O39)(H2O)3]6– and [Eu(PW11O39)2]11–. The host– guest interaction has a strong influence on the nature of the final intercalated species, as evidenced by elemental analy- Introduction Layered double hydroxides are an important class of ionic lamellar solids with the general formula [M2+ 1–xM3+ x(OH)2](Am–)x/m·nH2O (M2+ = Mg2+, Zn2+, Ni2+ etc., M3+ = Al3+, Cr3+, Ga3+ etc).[1] The positively charged layers, containing divalent and trivalent cations in octahedral positions, are separated by charge balancing anions and water molecules. The water molecules are connected to both the metal hydroxide layers and the interlayer anions through extensive hydrogen bonding. A range of organic or inorganic guests may be incorporated into LDHs by either ion exchange, direct synthesis or hydrothermal reconstruction of calcined precursors.[2,3] In particular, intercalation chemistry has been explored with the aim of introducing catalytically active sites and photo- and electroactive species. Many different types of metal coordination compounds and oxometalates have been immobilized in LDHs, including phthalocyanines, cyanocomplexes, oxalate complexes and polyoxometalates (POMs).[4] The first report of LDHs containing polyoxometalates concerned their use as exhaust gas and hydrocarbon conversion catalysts.[5] Since then, a variety of iso- and heteropolyanions with different nuclearities and structures (Keggin, Dawson, Preyssler, Finke) have been incorporated into the interlayer space of these materials.[6–18] Two factors assume considerable importance for the successful intercalation of polyoxometalates into an LDH compound. First, the heteropoly species should carry sufficient charge in order to be [a] Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal E-mail: helena@dq.ua.pt [b] Department of Physics, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal © 2006 Wiley-VCH Verlag 726 GmbH & Co. KGaA, Weinheim Eur. J. Inorg. Chem. 2006, 726–734 sis, powder X-ray diffraction (XRD), infra-red (IR) and Raman spectroscopy, solid state magic-angle spinning (MAS) 11B and 31P NMR spectroscopy, and photoluminescence spectroscopy.
publishDate 2006
dc.date.none.fl_str_mv 2006-02
2006-02-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/5716
url http://hdl.handle.net/10773/5716
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1434-1948
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
publisher.none.fl_str_mv WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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