Anchoring an Iridium Pincer Complex in a Hydrophobic Microporous Polymer for Application in Continuous‐Flow Alkane Dehydrogenation

dc.contributor.authorKönig, Michaela
dc.contributor.authorTraxler, Michael
dc.contributor.authorRudolph, Maik Alexander
dc.contributor.authorSchmidt, Johannes
dc.contributor.authorKüçükkeçeci, Hüseyin
dc.contributor.authorSchomäcker, Reinhard
dc.contributor.authorThomas, Arne
dc.date.accessioned2022-12-15T12:51:02Z
dc.date.available2022-12-15T12:51:02Z
dc.date.issued2022-08-18
dc.date.updated2022-11-22T16:56:31Z
dc.description.abstractAn iridium pincer complex {p‐KO‐C6H2‐2,6‐[OP(t‐Bu)2]2}Ir(C2H4) is immobilized in a propyl bromide‐functionalized microporous polymer network using the concepts of surface organometallic chemistry. The support material enables the formation of isolated active metal sites embedded in a chemically robust and highly hydrophobic environment. The catalyst maintained high porosity and – without prior activation – exhibited high activity in the continuous‐flow dehydrogenation of cyclohexane at elevated temperatures. The catalyst shows a stable performance for at least 7 days, even when additional H2O was co‐fed, owing to its hydrophobic nature.en
dc.description.sponsorshipDFG, 390540038, EXC 2008: Unifying Systems in Catalysis "UniSysCat"
dc.description.sponsorshipTU Berlin, Open-Access-Mittel – 2022
dc.identifier.eissn1867-3899
dc.identifier.issn1867-3880
dc.identifier.urihttps://depositonce.tu-berlin.de/handle/11303/17818
dc.identifier.urihttps://doi.org/10.14279/depositonce-16607
dc.language.isoen
dc.relation.ispartof10.14279/depositonce-16653
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540 Chemie und zugeordnete Wissenschaftende
dc.subject.othercatalysis
dc.subject.otherdehydrogenation
dc.subject.othermicroporous polymer network
dc.subject.otherpincer
dc.titleAnchoring an Iridium Pincer Complex in a Hydrophobic Microporous Polymer for Application in Continuous‐Flow Alkane Dehydrogenationen
dc.typeArticle
dc.type.versionpublishedVersion
dcterms.bibliographicCitation.articlenumbere202200811
dcterms.bibliographicCitation.doi10.1002/cctc.202200811
dcterms.bibliographicCitation.issue18
dcterms.bibliographicCitation.journaltitleChemCatChemen
dcterms.bibliographicCitation.originalpublishernameWiley
dcterms.bibliographicCitation.originalpublisherplaceNew York, NY
dcterms.bibliographicCitation.volume14
tub.accessrights.dnbfree
tub.affiliationFak. 2 Mathematik und Naturwissenschaften::Inst. Chemie::FG Funktionsmaterialien
tub.publisher.universityorinstitutionTechnische Universität Berlin

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