Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis

Detalhes bibliográficos
Autor(a) principal: Neves, Patrícia
Data de Publicação: 2024
Outros Autores: Gomes, Ana C., Monteiro, Rodrigo P., Santos, Mirela J., Valente, Anabela A., Lopes, André D., Gonçalves, Isabel S., Pillinger, Martyn
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/42485
Resumo: There are very few known examples of supramolecular compounds comprising molybdenum species hosted inside the portals/cavities of cucurbit[n]urils (CBn). In this work, CB7 and CB8 macrocycles have been studied as hosts for the carbonyl complex [CpMo(CO)3Me] (1) (Cp = η5-C5H5). Compounds were isolated in the solid state and characterized as genuine 1:1 inclusion complexes (1@CBn) by elemental and thermogravimetric analyses, powder X-ray diffraction, scanning electron microscopy, 13C{1H} cross-polarization magic-angle spinning NMR, FT-IR, Raman, and diffuse reflectance UV–Vis spectroscopies. The host–guest structures can act as supramolecular precatalysts for olefin epoxidation. Based on the model reaction of cis-cyclooctene with hydroperoxide oxidants (tert-butylhydroperoxide or hydrogen peroxide), the structural features of 1@CBn as well as the operating conditions influence the catalytic process. The metal species in 1@CBn undergo oxidative decarbonylation in situ, giving oxidized metal species that are catalytically active for olefin epoxidation. The type of oxidant and solvent influences the catalytic activity and stability. 1@CB8 was more stable than 1@CB7 with regard to catalyst recycling and reuse. Based on the substrate scope investigation, for relatively large olefins, such as the fatty acid methyl ester methyl oleate, the size of the macrocyclic host may be a determining factor for catalytic activity.
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spelling Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysisCarbonyl complexesCucurbiturilsInclusion compoundsMolybdenumOlefin epoxidationThere are very few known examples of supramolecular compounds comprising molybdenum species hosted inside the portals/cavities of cucurbit[n]urils (CBn). In this work, CB7 and CB8 macrocycles have been studied as hosts for the carbonyl complex [CpMo(CO)3Me] (1) (Cp = η5-C5H5). Compounds were isolated in the solid state and characterized as genuine 1:1 inclusion complexes (1@CBn) by elemental and thermogravimetric analyses, powder X-ray diffraction, scanning electron microscopy, 13C{1H} cross-polarization magic-angle spinning NMR, FT-IR, Raman, and diffuse reflectance UV–Vis spectroscopies. The host–guest structures can act as supramolecular precatalysts for olefin epoxidation. Based on the model reaction of cis-cyclooctene with hydroperoxide oxidants (tert-butylhydroperoxide or hydrogen peroxide), the structural features of 1@CBn as well as the operating conditions influence the catalytic process. The metal species in 1@CBn undergo oxidative decarbonylation in situ, giving oxidized metal species that are catalytically active for olefin epoxidation. The type of oxidant and solvent influences the catalytic activity and stability. 1@CB8 was more stable than 1@CB7 with regard to catalyst recycling and reuse. Based on the substrate scope investigation, for relatively large olefins, such as the fatty acid methyl ester methyl oleate, the size of the macrocyclic host may be a determining factor for catalytic activity.Wiley2024-09-20T13:49:32Z2024-05-01T00:00:00Z2024-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/42485eng0268-260510.1002/aoc.7412Neves, PatríciaGomes, Ana C.Monteiro, Rodrigo P.Santos, Mirela J.Valente, Anabela A.Lopes, André D.Gonçalves, Isabel S.Pillinger, Martyninfo: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:RCAAP2024-09-23T01:47:02Zoai:ria.ua.pt:10773/42485Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-09-23T01:47:02Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
title Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
spellingShingle Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
Neves, Patrícia
Carbonyl complexes
Cucurbiturils
Inclusion compounds
Molybdenum
Olefin epoxidation
title_short Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
title_full Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
title_fullStr Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
title_full_unstemmed Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
title_sort Inclusion complexes of cucurbit[n]urils (n = 7, 8) with η5‐cyclopentadienyl methyl tricarbonyl molybdenum(II) and their use in epoxidation catalysis
author Neves, Patrícia
author_facet Neves, Patrícia
Gomes, Ana C.
Monteiro, Rodrigo P.
Santos, Mirela J.
Valente, Anabela A.
Lopes, André D.
Gonçalves, Isabel S.
Pillinger, Martyn
author_role author
author2 Gomes, Ana C.
Monteiro, Rodrigo P.
Santos, Mirela J.
Valente, Anabela A.
Lopes, André D.
Gonçalves, Isabel S.
Pillinger, Martyn
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Neves, Patrícia
Gomes, Ana C.
Monteiro, Rodrigo P.
Santos, Mirela J.
Valente, Anabela A.
Lopes, André D.
Gonçalves, Isabel S.
Pillinger, Martyn
dc.subject.por.fl_str_mv Carbonyl complexes
Cucurbiturils
Inclusion compounds
Molybdenum
Olefin epoxidation
topic Carbonyl complexes
Cucurbiturils
Inclusion compounds
Molybdenum
Olefin epoxidation
description There are very few known examples of supramolecular compounds comprising molybdenum species hosted inside the portals/cavities of cucurbit[n]urils (CBn). In this work, CB7 and CB8 macrocycles have been studied as hosts for the carbonyl complex [CpMo(CO)3Me] (1) (Cp = η5-C5H5). Compounds were isolated in the solid state and characterized as genuine 1:1 inclusion complexes (1@CBn) by elemental and thermogravimetric analyses, powder X-ray diffraction, scanning electron microscopy, 13C{1H} cross-polarization magic-angle spinning NMR, FT-IR, Raman, and diffuse reflectance UV–Vis spectroscopies. The host–guest structures can act as supramolecular precatalysts for olefin epoxidation. Based on the model reaction of cis-cyclooctene with hydroperoxide oxidants (tert-butylhydroperoxide or hydrogen peroxide), the structural features of 1@CBn as well as the operating conditions influence the catalytic process. The metal species in 1@CBn undergo oxidative decarbonylation in situ, giving oxidized metal species that are catalytically active for olefin epoxidation. The type of oxidant and solvent influences the catalytic activity and stability. 1@CB8 was more stable than 1@CB7 with regard to catalyst recycling and reuse. Based on the substrate scope investigation, for relatively large olefins, such as the fatty acid methyl ester methyl oleate, the size of the macrocyclic host may be a determining factor for catalytic activity.
publishDate 2024
dc.date.none.fl_str_mv 2024-09-20T13:49:32Z
2024-05-01T00:00:00Z
2024-05
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/10773/42485
url http://hdl.handle.net/10773/42485
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0268-2605
10.1002/aoc.7412
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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