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Dry reforming of methane can so far afford syngas with equimolar CO and H2, which is suboptimal for Fischer–Tropsch chemistry. Now a process is reported based on a Ni–In molten metal alloy catalyst that is capable of producing syngas with practically relevant H2/CO ratios together with separable carbon.
The organocatalysed addition of aldehydes to nitroolefins is an extremely well-studied reaction that almost exclusively provides the syn-configured products. Here a general method to reverse the diastereoselectivity is reported, whereby a tripeptide catalyst consistently provides the anti product with high selectivity.
Amide reduction via hydroboration is challenging, and catalysts often exhibit limited substrate scope. Here the authors report synthesis of a lanthanum cluster as a catalyst for the hydroboration of esters and amides, capable of reducing a wide range of primary, secondary and tertiary amides to amines.
In order to use early, non-noble transition metals in homogeneous catalysis, complex ligands are typically needed, offsetting the benefits of inexpensive metals. Here the authors show that a simple manganese complex can be used in the hydrogenation of N-heteroarenes, without the need for additional ligands.
Electrochemical 2e− water oxidation is a promising route for renewable H2O2 production but it suffers from low selectivity due to the competing 4e− process. Here the authors demonstrate an interfacial engineering approach where the catalyst is coated with a hydrophobic polymer to confine in situ produced O2 and promote the 2e− pathway.
Investigation of proximity-driven enzyme regulation in intracellular signalling could benefit from suitable model systems. This work reports the engineering of a synthetic DNA origami-based apoptosome facilitating detailed analysis of caspase-9 activation, which is essential in programmed cell death.
Genetic incorporation of unnatural amino acids into proteins broadens the possibilities of enzyme design. This Perspective discusses the exciting opportunities for biocatalysis offered by this method — such as new-to-nature catalytic activities — and potential benefits over classical enzyme engineering.
Ethylene glycol is a commodity chemical with an annual consumption of 20 million tonnes. Its production generates 1.6 tonnes of CO2 per tonne of ethylene glycol. To reduce these CO2 emissions, the authors report a one-step electrochemical route to selectively convert ethylene to ethylene glycol at ambient temperature and pressure in aqueous media.
Identifying rate-determining steps (RDSs) is one of the most challenging aspects of catalysis. This work presents a general framework to identify the RDS of mixed ion and electron transfer reactions, and applies it to the four-electron/two-ion O2 reduction in solid-oxide fuel cell cathodes, converging on four RDS out of more than 100 possible candidates.
