Benzo-15-crown-5 ether supported on multi-wall carbon nanotubes (MWCNTs) by tethered poly(amidoamine) (PAMAM) dendrimers efficiently coordinated methyltrioxorhenium in the selective oxidation of olefins to epoxides. Environmentally friendly hydrogen peroxide was used as a primary oxidant. Up to first and second generation dendrimer aggregates were prepared by applying a divergent PAMAM methodology. FT-IR, XRD and ICP-MS analyses confirmed the effective coordination of methyltrioxorhenium by the benzo-15-crown-5 ether moiety after immobilization on MWCNTs. The novel catalysts converted olefins to the corresponding epoxides in high yield without the use of Lewis base additives, or anhydrous hydrogen peroxide, the catalyst being stable for more than six oxidative runs. In the absence of the PAMAM structure, the synthesis of diols largely prevailed.
Dendrimer crown-ether tethered multi-wall carbon nanotubes support methyltrioxorhenium in the selective oxidation of olefins to epoxides / Bizzarri, Bruno Mattia; Fanelli, Angelica; Botta, Lorenzo; Sadun, Claudia; Gontrani, Lorenzo; Ferella, Francesco; Crucianelli, Marcello; Saladino, Raffaele. - In: RSC ADVANCES. - ISSN 2046-2069. - 10:29(2020), pp. 17185-17194. [10.1039/D0RA02785E]
Dendrimer crown-ether tethered multi-wall carbon nanotubes support methyltrioxorhenium in the selective oxidation of olefins to epoxides
Fanelli, Angelica;Sadun, Claudia;Gontrani, Lorenzo;
2020
Abstract
Benzo-15-crown-5 ether supported on multi-wall carbon nanotubes (MWCNTs) by tethered poly(amidoamine) (PAMAM) dendrimers efficiently coordinated methyltrioxorhenium in the selective oxidation of olefins to epoxides. Environmentally friendly hydrogen peroxide was used as a primary oxidant. Up to first and second generation dendrimer aggregates were prepared by applying a divergent PAMAM methodology. FT-IR, XRD and ICP-MS analyses confirmed the effective coordination of methyltrioxorhenium by the benzo-15-crown-5 ether moiety after immobilization on MWCNTs. The novel catalysts converted olefins to the corresponding epoxides in high yield without the use of Lewis base additives, or anhydrous hydrogen peroxide, the catalyst being stable for more than six oxidative runs. In the absence of the PAMAM structure, the synthesis of diols largely prevailed.File | Dimensione | Formato | |
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