A divacant Keggin polyanion has been decorated with a N-heterocyclic carbene (NHC) iridium(I) organometallic complex to provide a molecular model of an Ir-based supported catalyst. The characterization of the hybrid compound has been performed by multinuclear NMR spectroscopy, infrared spectroscopy, cyclic voltammetry, and mass spectroscopy, and the results are in agreement with a bisfunctionalization of the polyoxometalate scaffold. The resulting supported homogeneous complex has been successfully used to catalyze the transfer hydrogenation from iPrOH to benzophenone [with a turnover number (TON) of 680 and a turnover frequency (TOF) of up to 540 h–1].

Transfer Hydrogenation Catalysis by a N-Heterocyclic Carbene Iridium Complex on a Polyoxometalate Platform

MODUGNO, GLORIA;BONCHIO, MARCELLA;CARRARO, MAURO
2014

Abstract

A divacant Keggin polyanion has been decorated with a N-heterocyclic carbene (NHC) iridium(I) organometallic complex to provide a molecular model of an Ir-based supported catalyst. The characterization of the hybrid compound has been performed by multinuclear NMR spectroscopy, infrared spectroscopy, cyclic voltammetry, and mass spectroscopy, and the results are in agreement with a bisfunctionalization of the polyoxometalate scaffold. The resulting supported homogeneous complex has been successfully used to catalyze the transfer hydrogenation from iPrOH to benzophenone [with a turnover number (TON) of 680 and a turnover frequency (TOF) of up to 540 h–1].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2832909
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