Novel Application of Polymer Networks Carrying Tertiary Amines as a Catalyst Inside Microflow Reactors Used for Knoevenagel Reactions

dc.bibliographicCitation.firstPage5765eng
dc.bibliographicCitation.issue35eng
dc.bibliographicCitation.journalTitleEuropean journal of organic chemistryeng
dc.bibliographicCitation.lastPage5774eng
dc.bibliographicCitation.volume2020eng
dc.contributor.authorBerg, Patrik
dc.contributor.authorObst, Franziska
dc.contributor.authorSimon, David
dc.contributor.authorRichter, Andreas
dc.contributor.authorAppelhans, Dietmar
dc.contributor.authorKuckling, Dirk
dc.date.accessioned2021-09-28T07:06:03Z
dc.date.available2021-09-28T07:06:03Z
dc.date.issued2020
dc.description.abstractA novel application is described for utilizing hydrogel dots as organocatalyst carriers inside microfluidic reactors. Tertiary amines were covalently immobilized in the hydrogel dots. Due to the diffusion of reactants within the swollen hydrogel dots, the accessible amount of catalysts inside a microfluidic reactor chamber can be increased compared to the accessible amount of surface-bound catalysts. To perform fast Knoevenagel reactions, important flow parameters had to be validated to optimize the reactor performance while keeping the dimensions of the reactor chamber constant; e.g. the height of the hydrogel dots had to be adjusted to the invariable dimensions of the reactor chamber, or an adjustment of organocatalysts in the hydrogel dots had to be validated to achieve the highest conversion rate during a certain residence time. To characterize the conversion, nuclear magnetic resonance (NMR) and UV/Vis-spectroscopy were utilized as an offline and online method, respectively. With suitable hydrogel dots, the influence of different flow parameters (e.g., operating flow rate and reactant concentration) on the selected model reactions in the microfluidic reactor was investigated. Finally, a variety of reactants were screened with the optimized flow parameters. With these results, the turnover frequency was determined for the Knoevenagel reactions in a microfluidic reactor, and the results were compared with published data that were determined by other synthetic approaches. © 2020 The Authors published by Wiley-VCH GmbHeng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/6920
dc.identifier.urihttps://doi.org/10.34657/5967
dc.language.isoengeng
dc.publisherWeinheim : Wiley-VCH Verl.eng
dc.relation.doihttps://doi.org/10.1002/ejoc.202000978
dc.relation.essn1099-0690
dc.relation.issn1434-193X
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.otherGreen chemistryeng
dc.subject.otherHydrogel dotseng
dc.subject.otherImmobilized organocatalystseng
dc.subject.otherMicrofluidic reactoreng
dc.subject.otherOrganocatalytic reactioneng
dc.titleNovel Application of Polymer Networks Carrying Tertiary Amines as a Catalyst Inside Microflow Reactors Used for Knoevenagel Reactionseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPHTeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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