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Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks

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Resumo:The confinement and catalytic behavior of Mo(CO)6 species inside UiO-66 (zirconium and hafnium) metalorganic frameworks (MOFs) have been investigated by means of multitechnique characterization and catalytic olefin epoxidation. Mo(CO)6 was encapsulated in nanocrystalline MOFs by solvothermal and vapor phase impregnation methods (STI and VPI, respectively), resulting in Mo loadings of 2.0–8.8 wt% (STI) or 15 wt% (VPI). Powder X-ray diffraction, SEM-EDS, N2 adsorption, FT-IR and 13C{1H} CP MAS NMR collectively confirmed immobilization within the pore spaces of the hosts, which maintained their bulk crystallinity and crystal morphologies. CO resonances in the 13C{1H} CP MAS NMR spectra were assigned to hexacarbonyl guest molecules located in the larger pore spaces, such as the octahedral cavities (for STI and VPI samples), and in more restricted environments such as the tetrahedral cavities (for the VPI sample). FT-IR spectra displayed the characteristic pattern of νCO stretching modes for an octahedral symmetry molecule slightly perturbed by interaction of one of the carbonyl groups with the MOF support. The spectra evidenced the formation of a weak hydrogen bonding interaction of the type μ3-OH⋅⋅⋅OCMo(CO)5 involving the μ3-OH groups that are exclusively present in the tetrahedral cavities of the UiO-66 structure. The Mo(CO)6 loaded MOFs are active and reusable pre-catalysts for cis-cyclooctene epoxidation, exhibiting excellent epoxide selectivity (up to quantitative epoxide yield within 1 h reaction) and tert-butyl hydroperoxide efficiency. Catalyst recycling and retention of structural integrity were demonstrated for UiO-66(Hf) loaded with 8.8 wt% Mo by the STI method. The UiO-66(Hf) host may be a better catalyst support than its Zr counterpart due its smaller crystallite size (≈100 nm) and higher defectivity. The substrate scope was broadened for Mo(8.8-STI)/Hf-MOF which promoted the epoxidation of biobased olefins (methyl oleate and DL-limonene) and oxidative dehydrogenation of cyclooctanol to cyclooctanone.
Autores principais:Gomes, Diana P.
Outros Autores:Silva, Andreia F.; Gomes, Ana C.; Neves, Patrícia; Valente, Anabela A.; Gonçalves, Isabel S.; Pillinger, Martyn
Assunto:Molybdenum hexacarbonyl cis-Cyclooctene Tert-butyl hydroperoxide Metal-organic framework Epoxidation
Ano:2022
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso restrito
Instituição associada:Universidade de Aveiro
Idioma:inglês
Origem:RIA - Repositório Institucional da Universidade de Aveiro
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author Gomes, Diana P.
author2 Silva, Andreia F.
Gomes, Ana C.
Neves, Patrícia
Valente, Anabela A.
Gonçalves, Isabel S.
Pillinger, Martyn
author2_role author
author
author
author
author
author
author_facet Gomes, Diana P.
Silva, Andreia F.
Gomes, Ana C.
Neves, Patrícia
Valente, Anabela A.
Gonçalves, Isabel S.
Pillinger, Martyn
author_role author
country_str PT
creators_json_txt [{\"Person.name\":\"Gomes, Diana P.\"},{\"Person.name\":\"Silva, Andreia F.\"},{\"Person.name\":\"Gomes, Ana C.\"},{\"Person.name\":\"Neves, Patrícia\"},{\"Person.name\":\"Valente, Anabela A.\"},{\"Person.name\":\"Gonçalves, Isabel S.\"},{\"Person.name\":\"Pillinger, Martyn\"}]
datacite.creators.creator.creatorName.fl_str_mv Gomes, Diana P.
Silva, Andreia F.
Gomes, Ana C.
Neves, Patrícia
Valente, Anabela A.
Gonçalves, Isabel S.
Pillinger, Martyn
datacite.date.Accepted.fl_str_mv 2022-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2022-07-27T10:29:53Z
datacite.date.embargoed.fl_str_mv 2022-07-27T10:29:53Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_16ec
datacite.subjects.subject.fl_str_mv Molybdenum hexacarbonyl
cis-Cyclooctene
Tert-butyl hydroperoxide
Metal-organic framework
Epoxidation
datacite.titles.title.fl_str_mv Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
dc.creator.none.fl_str_mv Gomes, Diana P.
Silva, Andreia F.
Gomes, Ana C.
Neves, Patrícia
Valente, Anabela A.
Gonçalves, Isabel S.
Pillinger, Martyn
dc.date.Accepted.fl_str_mv 2022-01-01T00:00:00Z
dc.date.available.fl_str_mv 2022-07-27T10:29:53Z
dc.date.embargoed.fl_str_mv 2022-07-27T10:29:53Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv http://hdl.handle.net/10773/34328
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Elsevier
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_16ec
dc.subject.none.fl_str_mv Molybdenum hexacarbonyl
cis-Cyclooctene
Tert-butyl hydroperoxide
Metal-organic framework
Epoxidation
dc.title.fl_str_mv Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description The confinement and catalytic behavior of Mo(CO)6 species inside UiO-66 (zirconium and hafnium) metalorganic frameworks (MOFs) have been investigated by means of multitechnique characterization and catalytic olefin epoxidation. Mo(CO)6 was encapsulated in nanocrystalline MOFs by solvothermal and vapor phase impregnation methods (STI and VPI, respectively), resulting in Mo loadings of 2.0–8.8 wt% (STI) or 15 wt% (VPI). Powder X-ray diffraction, SEM-EDS, N2 adsorption, FT-IR and 13C{1H} CP MAS NMR collectively confirmed immobilization within the pore spaces of the hosts, which maintained their bulk crystallinity and crystal morphologies. CO resonances in the 13C{1H} CP MAS NMR spectra were assigned to hexacarbonyl guest molecules located in the larger pore spaces, such as the octahedral cavities (for STI and VPI samples), and in more restricted environments such as the tetrahedral cavities (for the VPI sample). FT-IR spectra displayed the characteristic pattern of νCO stretching modes for an octahedral symmetry molecule slightly perturbed by interaction of one of the carbonyl groups with the MOF support. The spectra evidenced the formation of a weak hydrogen bonding interaction of the type μ3-OH⋅⋅⋅OCMo(CO)5 involving the μ3-OH groups that are exclusively present in the tetrahedral cavities of the UiO-66 structure. The Mo(CO)6 loaded MOFs are active and reusable pre-catalysts for cis-cyclooctene epoxidation, exhibiting excellent epoxide selectivity (up to quantitative epoxide yield within 1 h reaction) and tert-butyl hydroperoxide efficiency. Catalyst recycling and retention of structural integrity were demonstrated for UiO-66(Hf) loaded with 8.8 wt% Mo by the STI method. The UiO-66(Hf) host may be a better catalyst support than its Zr counterpart due its smaller crystallite size (≈100 nm) and higher defectivity. The substrate scope was broadened for Mo(8.8-STI)/Hf-MOF which promoted the epoxidation of biobased olefins (methyl oleate and DL-limonene) and oxidative dehydrogenation of cyclooctanol to cyclooctanone.
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identifier.url.fl_str_mv http://hdl.handle.net/10773/34328
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institution Universidade de Aveiro
instname_str Universidade de Aveiro
language eng
network_acronym_str ria
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oai_identifier_str oai:ria.ua.pt:10773/34328
organization_str_mv urn:organizationAcronym:ua
person_str_mv Gomes, Diana P.
Silva, Andreia F.
Gomes, Ana C.
Neves, Patrícia
Valente, Anabela A.
Gonçalves, Isabel S.
Pillinger, Martyn
publishDate 2022
publisher.none.fl_str_mv Elsevier
reponame_str RIA - Repositório Institucional da Universidade de Aveiro
repository_id_str urn:repositoryAcronym:ria
service_str_mv urn:repositoryAcronym:ria
spelling pt_PTThe confinement and catalytic behavior of Mo(CO)6 species inside UiO-66 (zirconium and hafnium) metalorganic frameworks (MOFs) have been investigated by means of multitechnique characterization and catalytic olefin epoxidation. Mo(CO)6 was encapsulated in nanocrystalline MOFs by solvothermal and vapor phase impregnation methods (STI and VPI, respectively), resulting in Mo loadings of 2.0–8.8 wt% (STI) or 15 wt% (VPI). Powder X-ray diffraction, SEM-EDS, N2 adsorption, FT-IR and 13C{1H} CP MAS NMR collectively confirmed immobilization within the pore spaces of the hosts, which maintained their bulk crystallinity and crystal morphologies. CO resonances in the 13C{1H} CP MAS NMR spectra were assigned to hexacarbonyl guest molecules located in the larger pore spaces, such as the octahedral cavities (for STI and VPI samples), and in more restricted environments such as the tetrahedral cavities (for the VPI sample). FT-IR spectra displayed the characteristic pattern of νCO stretching modes for an octahedral symmetry molecule slightly perturbed by interaction of one of the carbonyl groups with the MOF support. The spectra evidenced the formation of a weak hydrogen bonding interaction of the type μ3-OH⋅⋅⋅OCMo(CO)5 involving the μ3-OH groups that are exclusively present in the tetrahedral cavities of the UiO-66 structure. The Mo(CO)6 loaded MOFs are active and reusable pre-catalysts for cis-cyclooctene epoxidation, exhibiting excellent epoxide selectivity (up to quantitative epoxide yield within 1 h reaction) and tert-butyl hydroperoxide efficiency. Catalyst recycling and retention of structural integrity were demonstrated for UiO-66(Hf) loaded with 8.8 wt% Mo by the STI method. The UiO-66(Hf) host may be a better catalyst support than its Zr counterpart due its smaller crystallite size (≈100 nm) and higher defectivity. The substrate scope was broadened for Mo(8.8-STI)/Hf-MOF which promoted the epoxidation of biobased olefins (methyl oleate and DL-limonene) and oxidative dehydrogenation of cyclooctanol to cyclooctanone.application/pdfengElsevierpt_PTEpoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworksGomes, Diana P.Silva, Andreia F.Gomes, Ana C.Neves, PatríciaValente, Anabela A.Gonçalves, Isabel S.Pillinger, MartynHandlehttp://hdl.handle.net/10773/34328ISSNIsPartOf1387-1811DOIIsPartOf10.1016/j.micromeso.2021.1116032022-07-27T10:29:53Z2022-01-01T00:00:00Z2022-01http://purl.org/coar/access_right/c_16ecrestricted accesspt_PTMolybdenum hexacarbonylpt_PTcis-Cyclooctenept_PTTert-butyl hydroperoxidept_PTMetal-organic frameworkpt_PTEpoxidation6513854 byteshttp://purl.org/coar/access_right/c_16ecapplication/pdffulltexthttps://ria.ua.pt/bitstream/10773/34328/1/Microporous%20and%20Mesoporous%20Materials%20330%20%282022%29%20111603.pdfliteraturehttp://purl.org/coar/resource_type/c_6501journal article
spellingShingle Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
Gomes, Diana P.
Molybdenum hexacarbonyl
cis-Cyclooctene
Tert-butyl hydroperoxide
Metal-organic framework
Epoxidation
status SINGLETON
subject.fl_str_mv Molybdenum hexacarbonyl
cis-Cyclooctene
Tert-butyl hydroperoxide
Metal-organic framework
Epoxidation
title Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
title_full Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
title_fullStr Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
title_full_unstemmed Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
title_short Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
title_sort Epoxidation catalysts prepared by encapsulation of molybdenum hexacarbonyl in UiO-66(Zr/Hf)-type metal-organic frameworks
topic Molybdenum hexacarbonyl
cis-Cyclooctene
Tert-butyl hydroperoxide
Metal-organic framework
Epoxidation
topic_facet Molybdenum hexacarbonyl
cis-Cyclooctene
Tert-butyl hydroperoxide
Metal-organic framework
Epoxidation
url http://hdl.handle.net/10773/34328
visible 1