Single-Site Metal Organic Complexes on Oxide Supports for Selective Alkane Functionalization

Tait, Steven L.

doi:10.2172/1797443

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DOE OSTI · 1797443

Single-Site Metal Organic Complexes on Oxide Supports for Selective Alkane Functionalization

Tait, Steven L.

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Abstract

High levels of reaction selectivity for heterogeneous catalysis are generally difficult to achieve with traditional metal nanoparticle catalysts, due to the variety of metal binding sites available. In this project, we have developed a metal-ligand coordination strategy to form transition metal single-sites on high surface area supports as heterogeneous single-site catalysts. Metal centers can be atomically dispersed in the binding pockets of organic ligands on oxide supports. The systems have to be carefully designed so that tendencies for metal cluster formation or binding to surface defect sites are overcome by the attractive coordination environment provided by the organic ligand. This was confirmed by a comprehensive set of characterization methods, including XAS, XPS, XRD, TEM, and CO adsorption. Design and tuning of metal-support and support-ligand interactions were crucial for high structural uniformity. We demonstrate that supported metal-ligand SSCs are effective, recyclable catalysts for alkene hydrosilylation reactions. Compared with commercial homogeneous catalysts, they exhibit improved yield and selectivity, less metal aggregation and side reactions, and stronger tolerance with functionalized substrates. These results give some preliminary indication that coordination with organic ligands can improve activity and selectivity in metal/oxide heterogeneous catalysts.

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37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY heterogeneous catalysis hydrosilylation single-atom catalyst single-site catalyst

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Tait, Steven L.. 2021-06-17. Single-Site Metal Organic Complexes on Oxide Supports for Selective Alkane Functionalization. https://doi.org/10.2172/1797443

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