Synthesis and Characterization of Co(II) Substituted Keggin‐Type Polyoxometalates as Novel Catalysts for the Hydroformylation of 1‐Hexene in a Thermomorphic Solvent System

Author:

Raabe Jan‐Christian1,Hombach Lea2,Poller Maximilian J.1,Collauto Alberto3,Roessler Maxie M.3,Vorholt Andreas2,Beine Anna Katharina24,Albert Jakob1ORCID

Affiliation:

1. Institute of Technical and Macromolecular Chemistry Hamburg University Bundesstr. 45 20146 Hamburg Germany

2. Max Planck Institute for Chemical Energy Conversion Stiftstraße 34–36 45470 Mülheim an der Ruhr Germany

3. Department of Chemistry and Centre for Pulse EPR Spectroscopy Imperial College London Molecular Sciences Research Hub White City Campus London W12 0BZ UK

4. Department of Mechanical Engineering University of Siegen Paul-Bonatz-Str. 9–11 Siegen 57076 Germany

Abstract

AbstractPolyoxometalates (POMs) are a unique class of metal oxides, being of huge interest for the catalysis society. CoII‐substituted phosphomolybdate POMs (namely H7[PCoMo11O40], H11[PCo2Mo10O40] and H15[PCo3Mo9O40]) have been successfully synthesized for the first time. The structure of the new CoII substituted POMs was solved by single‐crystal X‐ray diffraction as well as vibrational (FT‐IR and Raman) and nuclear magnetic/electron paramagnetic resonance (NMR and EPR) spectroscopy and found to be of the Keggin‐type. The Co‐POMs were then applied as molecular catalysts for the hydroformylation of 1‐hexene in a thermomorphic solvent mixture of water and 1‐butanol. This is the very first example of a 1st row transition metal POM acting as a hydroformylation catalyst achieving 46 % heptanal yield. The best results were obtained using H11[PCo2Mo10O40] as a catalyst at 140 °C, 150 bar CO/H2 1 : 2, and a reaction time of 4 h, paving the way for new POM‐based catalysts in hydroformylation reactions.

Funder

Engineering and Physical Sciences Research Council

Publisher

Wiley

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