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Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid

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Summary:The single-pot efficient oxidation of ethane to acetic acid catalysed by Au(I) or Au(III) compounds, chlorotriphenylphosphinegold(I) (1), chlorotrimethylphosphinegold(I) (2), 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidenegold(I) chloride (3), dichloro(2-pyridinecarboxylato)gold(III) (4), homogenous and supported on different carbon materials: activated carbon (AC), multi-walled carbon nanotubes (CNT) and carbon xerogel (CX), oxidised with nitric acid followed by treatment with NaOH (-ox-Na), is reported. The reactions were performed in water/acetonitrile. The materials were selective for the production of acetic acid, with no trace of by-products being detected. The best homogenous catalysts were complexes 2 and 3 which showed the highest ethane conversion and an acetic acid yield of ca. 21%, followed by 4 and 1. The heterogenised materials showed much better activity than the homogenous counterparts, with acetic acid yields up to 41.4% for 4@CNT-ox-Na, and remarkable selectivity (with acetic acid being the only product detected). The heterogenised catalysts with the best results were reused up to five cycles, with no significant loss of activity, and maintaining high selectivity for acetic acid. 4@CNT-ox-Na showed not only the best catalytic activity but also the best stability during the recycling runs.
Main Authors:Ribeiro, Ana P. C.
Other Authors:Matias, Inês A. S.; Carabineiro, Sónia A. C.; Martins, Luísa M. D. R. S.
Subject:Acetic acid Carbon Ethane oxidation Gold Heterogeneous catalysis Catalysis Physical and Theoretical Chemistry
Year:2022
Country:Portugal
Document type:article
Access type:open access
Associated institution:Universidade Nova de Lisboa
Language:English
Origin:Repositório Institucional da UNL
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author Ribeiro, Ana P. C.
author2 Matias, Inês A. S.
Carabineiro, Sónia A. C.
Martins, Luísa M. D. R. S.
author2_role author
author
author
author_facet Ribeiro, Ana P. C.
Matias, Inês A. S.
Carabineiro, Sónia A. C.
Martins, Luísa M. D. R. S.
author_role author
contributor_name_str_mv LAQV@REQUIMTE
DQ - Departamento de Química
MDPI - Multidisciplinary Digital Publishing Institute
RUN
country_str PT
creators_json_txt [{\"Person.name\":\"Ribeiro, Ana P. C.\"},{\"Person.name\":\"Matias, Inês A. S.\"},{\"Person.name\":\"Carabineiro, Sónia A. C.\"},{\"Person.name\":\"Martins, Luísa M. D. R. S.\"}]
datacite.contributors.contributor.contributorName.fl_str_mv LAQV@REQUIMTE
DQ - Departamento de Química
MDPI - Multidisciplinary Digital Publishing Institute
RUN
datacite.creators.creator.creatorName.fl_str_mv Ribeiro, Ana P. C.
Matias, Inês A. S.
Carabineiro, Sónia A. C.
Martins, Luísa M. D. R. S.
datacite.date.Accepted.fl_str_mv 2022-02-01T00:00:00Z
datacite.date.available.fl_str_mv 2022-02-17T23:19:48Z
datacite.date.embargoed.fl_str_mv 2022-02-17T23:19:48Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Acetic acid
Carbon
Ethane oxidation
Gold
Heterogeneous catalysis
Catalysis
Physical and Theoretical Chemistry
datacite.titles.title.fl_str_mv Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
dc.contributor.none.fl_str_mv LAQV@REQUIMTE
DQ - Departamento de Química
MDPI - Multidisciplinary Digital Publishing Institute
RUN
dc.creator.none.fl_str_mv Ribeiro, Ana P. C.
Matias, Inês A. S.
Carabineiro, Sónia A. C.
Martins, Luísa M. D. R. S.
dc.date.Accepted.fl_str_mv 2022-02-01T00:00:00Z
dc.date.available.fl_str_mv 2022-02-17T23:19:48Z
dc.date.embargoed.fl_str_mv 2022-02-17T23:19:48Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv http://hdl.handle.net/10362/133133
dc.language.none.fl_str_mv eng
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv Acetic acid
Carbon
Ethane oxidation
Gold
Heterogeneous catalysis
Catalysis
Physical and Theoretical Chemistry
dc.title.fl_str_mv Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description The single-pot efficient oxidation of ethane to acetic acid catalysed by Au(I) or Au(III) compounds, chlorotriphenylphosphinegold(I) (1), chlorotrimethylphosphinegold(I) (2), 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidenegold(I) chloride (3), dichloro(2-pyridinecarboxylato)gold(III) (4), homogenous and supported on different carbon materials: activated carbon (AC), multi-walled carbon nanotubes (CNT) and carbon xerogel (CX), oxidised with nitric acid followed by treatment with NaOH (-ox-Na), is reported. The reactions were performed in water/acetonitrile. The materials were selective for the production of acetic acid, with no trace of by-products being detected. The best homogenous catalysts were complexes 2 and 3 which showed the highest ethane conversion and an acetic acid yield of ca. 21%, followed by 4 and 1. The heterogenised materials showed much better activity than the homogenous counterparts, with acetic acid yields up to 41.4% for 4@CNT-ox-Na, and remarkable selectivity (with acetic acid being the only product detected). The heterogenised catalysts with the best results were reused up to five cycles, with no significant loss of activity, and maintaining high selectivity for acetic acid. 4@CNT-ox-Na showed not only the best catalytic activity but also the best stability during the recycling runs.
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eu_rights_str_mv openAccess
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inst_facet_str urn:organizationAcronym:unl{{{_:::_}}}Universidade Nova de Lisboa
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instname_str Universidade Nova de Lisboa
language eng
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network_name_str Repositório Institucional da UNL
oai_identifier_str oai:run.unl.pt:10362/133133
organization_str_mv urn:organizationAcronym:unl
person_str_mv Ribeiro, Ana P. C.
Matias, Inês A. S.
Carabineiro, Sónia A. C.
Martins, Luísa M. D. R. S.
publishDate 2022
repo_facet_str urn:repositoryAcronym:run{{{_:::_}}}Repositório Institucional da UNL
reponame_str Repositório Institucional da UNL
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spelling engenThe single-pot efficient oxidation of ethane to acetic acid catalysed by Au(I) or Au(III) compounds, chlorotriphenylphosphinegold(I) (1), chlorotrimethylphosphinegold(I) (2), 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidenegold(I) chloride (3), dichloro(2-pyridinecarboxylato)gold(III) (4), homogenous and supported on different carbon materials: activated carbon (AC), multi-walled carbon nanotubes (CNT) and carbon xerogel (CX), oxidised with nitric acid followed by treatment with NaOH (-ox-Na), is reported. The reactions were performed in water/acetonitrile. The materials were selective for the production of acetic acid, with no trace of by-products being detected. The best homogenous catalysts were complexes 2 and 3 which showed the highest ethane conversion and an acetic acid yield of ca. 21%, followed by 4 and 1. The heterogenised materials showed much better activity than the homogenous counterparts, with acetic acid yields up to 41.4% for 4@CNT-ox-Na, and remarkable selectivity (with acetic acid being the only product detected). The heterogenised catalysts with the best results were reused up to five cycles, with no significant loss of activity, and maintaining high selectivity for acetic acid. 4@CNT-ox-Na showed not only the best catalytic activity but also the best stability during the recycling runs.application/pdfenCommercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic AcidRibeiro, Ana P. C.Matias, Inês A. S.Carabineiro, Sónia A. C.Martins, Luísa M. D. R. S.LAQV@REQUIMTEDQ - Departamento de QuímicaMDPI - Multidisciplinary Digital Publishing InstituteHostingInstitutionOrganizationalRUNe-mailmailto:run@unl.ptrun@unl.ptISSNIsPartOf2073-4344URNIsPartOfPURE: 36734554URNIsPartOfPURE UUID: df9b2535-bd01-4db7-8187-8737140f3d27URNIsPartOfScopus: 85123540078URNIsPartOfORCID: /0000-0001-9913-4671/work/108412187URNIsPartOfWOS: 000770808200001DOIIsPartOf10.3390/catal120201652022-02-17T23:19:48Z2022-022022-02-01T00:00:00ZHandlehttp://hdl.handle.net/10362/133133http://purl.org/coar/access_right/c_abf2open accessAcetic acidCarbonEthane oxidationGoldHeterogeneous catalysisCatalysisPhysical and Theoretical Chemistry3124361 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://run.unl.pt/bitstreams/73eec90f-e2b6-4048-822e-0e193695931c/download
spellingShingle Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
Ribeiro, Ana P. C.
Acetic acid
Carbon
Ethane oxidation
Gold
Heterogeneous catalysis
Catalysis
Physical and Theoretical Chemistry
status SINGLETON
subject.fl_str_mv Acetic acid
Carbon
Ethane oxidation
Gold
Heterogeneous catalysis
Catalysis
Physical and Theoretical Chemistry
title Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
title_full Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
title_fullStr Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
title_full_unstemmed Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
title_short Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
title_sort Commercial Gold Complexes Supported on Functionalised Carbon Materials as Efficient Catalysts for the Direct Oxidation of Ethane to Acetic Acid
topic Acetic acid
Carbon
Ethane oxidation
Gold
Heterogeneous catalysis
Catalysis
Physical and Theoretical Chemistry
topic_facet Acetic acid
Carbon
Ethane oxidation
Gold
Heterogeneous catalysis
Catalysis
Physical and Theoretical Chemistry
url http://hdl.handle.net/10362/133133
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