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Dirhodium complex immobilization on modified cellulose for highly selective heterogeneous cyclopropanation reactions

Rösler, Lorenz ; Höfler, Mark V. ; Breitzke, Hergen ; Wissel, Till ; Herr, Kevin ; Heise, Henrike ; Gutmann, Torsten ; Buntkowsky, Gerd (2023)
Dirhodium complex immobilization on modified cellulose for highly selective heterogeneous cyclopropanation reactions.
In: Cellulose, 2022, 29 (11)
doi: 10.26083/tuprints-00024225
Artikel, Zweitveröffentlichung, Verlagsversion

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Kurzbeschreibung (Abstract)

A novel, efficient approach for the functionalization of microcrystalline cellulose (MCC) is presented. The as-obtained material allows the immobilization of chiral dirhodium catalysts preserving their enantioselectivity in asymmetric cyclopropanation reactions. As model, microcrystalline cellulose is modified with a polyethylene glycol derived linker, and Rh₂(S-DOSP)₄ is grafted on the material to produce a heterogeneous catalyst. SEM images at different stages of the immobilization show an unchanging uniform morphology, providing constantly good separation characteristics. The modification of the cellulose material with the polyethylene derived linker and the immobilization process are monitored using DNP enhanced ¹H → ¹³C CP MAS NMR, quantitative ¹⁹F MAS NMR, TGA and ICP-OES analysis, confirming the success of the immobilization as well as the stability of bonds between the used linker molecule and the cellulose material. Finally, the evaluation of the produced catalyst is demonstrated in the asymmetric cyclopropanation reaction between styrene and methyl(E)-2-diazo-4-phenylbut-3-enoate showing excellent enantioselectivity with an ee of nearly 90% over a wide temperature range as well as good recyclability characteristics in four consecutive catalysis cycles.

Typ des Eintrags: Artikel
Erschienen: 2023
Autor(en): Rösler, Lorenz ; Höfler, Mark V. ; Breitzke, Hergen ; Wissel, Till ; Herr, Kevin ; Heise, Henrike ; Gutmann, Torsten ; Buntkowsky, Gerd
Art des Eintrags: Zweitveröffentlichung
Titel: Dirhodium complex immobilization on modified cellulose for highly selective heterogeneous cyclopropanation reactions
Sprache: Englisch
Publikationsjahr: 2023
Ort: Darmstadt
Publikationsdatum der Erstveröffentlichung: 2022
Verlag: Springer Nature
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Cellulose
Jahrgang/Volume einer Zeitschrift: 29
(Heft-)Nummer: 11
DOI: 10.26083/tuprints-00024225
URL / URN: https://tuprints.ulb.tu-darmstadt.de/24225
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Herkunft: Zweitveröffentlichungsservice
Kurzbeschreibung (Abstract):

A novel, efficient approach for the functionalization of microcrystalline cellulose (MCC) is presented. The as-obtained material allows the immobilization of chiral dirhodium catalysts preserving their enantioselectivity in asymmetric cyclopropanation reactions. As model, microcrystalline cellulose is modified with a polyethylene glycol derived linker, and Rh₂(S-DOSP)₄ is grafted on the material to produce a heterogeneous catalyst. SEM images at different stages of the immobilization show an unchanging uniform morphology, providing constantly good separation characteristics. The modification of the cellulose material with the polyethylene derived linker and the immobilization process are monitored using DNP enhanced ¹H → ¹³C CP MAS NMR, quantitative ¹⁹F MAS NMR, TGA and ICP-OES analysis, confirming the success of the immobilization as well as the stability of bonds between the used linker molecule and the cellulose material. Finally, the evaluation of the produced catalyst is demonstrated in the asymmetric cyclopropanation reaction between styrene and methyl(E)-2-diazo-4-phenylbut-3-enoate showing excellent enantioselectivity with an ee of nearly 90% over a wide temperature range as well as good recyclability characteristics in four consecutive catalysis cycles.

Freie Schlagworte: Immobilization, Asymmetric cyclopropanation, Dirhodium, NMR spectroscopy, Dynamic nuclear polarization
Status: Verlagsversion
URN: urn:nbn:de:tuda-tuprints-242258
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 530 Physik
500 Naturwissenschaften und Mathematik > 540 Chemie
Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie
07 Fachbereich Chemie > Eduard Zintl-Institut
07 Fachbereich Chemie > Eduard Zintl-Institut > Fachgebiet Physikalische Chemie
Hinterlegungsdatum: 11 Jul 2023 11:45
Letzte Änderung: 02 Aug 2024 12:53
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