Ingenious fluorescence microscopy experiments have revealed palladium atoms liberated behaviour, helping answer unresolved questions about an important process for forming bonds between carbon atoms. The SuzukiMiyaura cross-coupling won Akira Suzuki a Nobel prize in chemistry in 2010, but there has been debate about whether solid palladium catalysts are dissolving or not.

Tito Scaianos team at the University of Ottawa found that palladium atoms dissolve and leach away from other atoms in nanoparticles, but then land back on the surface of their supporting material. These redeposited palladium atoms are active sites for the carboncarbon bond formation process, explains Paolo Costa, first author on the new paper.

Industrially, the SuzukiMiyaura reaction is frequently used for the synthesis of essential drugs, says Costa. Industry finds it easier to isolate and reuse solid catalysts than work with soluble versions. But this raises the question of whether the carboncarbon bond formation reaction happens on the catalyst surface, or whether the catalyst dissolves and potentially leaches away. Finding the correct answer is important since leaching processes often result in unwanted traces of toxic metal in drugs, raising the operating costs for purification and catalyst recovery, Costa says.

At first Scaiano, Costa and their colleague Deborah Sandrin used non-microscopy methods to distinguish whether solid or dissolved palladium was the active catalyst. Some of their results suggested mechanisms occurring at the palladium nanoparticle surface, while others indicated a leaching process.

Scaianos group then used total internal reflectance fluorescence (Tirf) microscopy to directly study the atoms at work. In this process they shine specific wavelengths of laser light across a region 100200nm above a microscope slide that contains mixtures including fluorescent dyes. The microscope detects the resulting fluorescence in high resolution, potentially down to around 20nm pixel sizes and captures events occurring on timescales of 100ms. Thats enough to capture important details about catalyst behaviour.

To study the SuzukiMiyaura reaction, the Ottawa team designed a novel chemical system. They started with a molecule that fluoresces green, which has two bromine atoms that enable it to participate in carboncarbon bond formation reactions. Adding 2-thienylboronic acid can make a monosubstituted molecule, and then a disubstituted one, which fluoresces red. Using Tirf the chemists tracked when they saw the products form, and where.

At first the team saw fluorescence bursts at the same place as the palladium nanoparticles. They therefore thought carboncarbon bond formation was only happening at the palladium nanoparticle surface. But a peer reviewer who assessed their paper prior to publication suggested that atoms could be leaching and readsorbing.

The chemists rose to this challenge. They placed an area of catalyst comprising palladium nanoparticles distributed on titanium dioxide support material side-by-side with an area of titanium dioxide containing no catalyst. They then let reagents flow from the catalyst side of the slide to the pure titanium dioxide side. To their surprise, they soon started to see fluorescence bursts originating on the pure side. Tirf microscopy demonstrated that the catalytic sites, atoms or small clusters of palladium, are active once they land back on the titanium dioxide support, highlighting the heterogeneous, yet mobile, nature of the catalytic system investigated, Costa underlines.

Vivek Polshettiwar, from the Tata Institute of Fundamental Research (TIFR) in Mumbai, India, says that leached palladium atoms becoming active sites after attachment back to catalyst supports is indeed an exciting finding. Most heterogeneous catalysts for Suzuki coupling use amine or thiol functionalised supports before loading palladium, adds Polshettiwar. This generally significantly reduces leaching, he notes. It will be interesting to know if these systems also follow the same mechanism.

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Palladium catalyst voyage prompts carboncarbon bond formation rethink - Chemistry World