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Article Released Tue-27th-June-2017 05:35 GMT
Contact: Koomi Sung Institution: Nagoya University
 Nagoya University chemists turn metal catalysis on its head for a sustainable future

Nagoya University team used high-valent transition metal catalysts for an unconventional hydrogenation of carboxylic acid groups, common to biomass feedstocks. The high-valent catalysts showed good selectivity under mild conditions.

High valence rhenium used to recycle organic waste for a carbon neutral society
A rhenium catalyst in a high oxidation state is used to hydrogenate carboxylic acids present in organic waste, producing a range of useful alcohol products.
Copyright : Nagoya University
Nagoya University researchers take a nonintuitive approach to metal catalysis for selective conversion of biomass into high-value chemical products under mild conditions.

The uncertain future of oil feedstocks and environmental pressure are forcing the chemical industry to adapt and find new renewable sources to sustain its activities. Biomass from sources including wood, agricultural waste, and even human garbage, represents a widely available renewable feedstock that has yet to be fully tapped. The problem is that most biomass is a mess of different chemicals, which are difficult to separate and use in high-value products such as plastics and pharmaceuticals.

Carboxylic acids are one of the most common chemical groups in biomass, and their chemical reactions are particularly difficult to control in these mixtures. Currently used “catalytic hydrogenation” with metal catalysts can transform the acids into more useful alcohol groups, but also adds to the complexity of the biomass because of other side reactions and catalyst decomposition.

Recognizing the need for more selective transformations of carboxylic acid groups, a team at Nagoya University explored a different chemical approach to the catalysis of biomass.

“Traditionally, low-valent transition metal complexes are used for hydrogenation of carboxylic acids. But we found better selectivity under milder conditions using a high-valent complex, which also attacked carbon-hydrogen bonds next to the carboxylic acid,” says lead author Masayuki Naruto.

Hydrogenation is essentially a reduction, during which the metal catalyzes transfer of electrons to the carboxylic acid. Low-valence metals are electron rich, which makes them the obvious choice for hydrogenation of carboxylic acids. However, the team showed that high valence metals could also react with the carboxylic acids by a different pathway, which offered much better control over the reactivity.

“The idea that high-valent transition metals are effective for this kind of reaction might go against traditional wisdom, but we have shown the potential of this approach for making high-value chemical products from biomass,” says group leader Susumu Saito. “Although, the rhenium metal catalyst we used here is rather expensive, we are now looking at recycling the catalyst and alternative tungsten and molybdenum catalysts, which should make this a truly economically viable approach for getting useful products from biomass in the future.”

Associated links

Journal information

The article, “Catalytic transformation of functionalized carboxylic acids using multifunctional rhenium complexes” was published in Scientific Reports at DOI: 10.1038/s41598-017-03436-y.

Funding information

Japan Science and Technology Agency, Ministry of Education, Culture, Sports, Science and Technology, Asahi Glass Foundation

Keywords associated to this article: Chemistry/Physics/Materials Sciences, Industrial Engineering/Chemistry Biochemistry, Energy/Fuel (non-petroleum), Polymer Chemistry
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