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Monodisperse perovskite nanocrystals are formed by using a diffusion-mediated growth mechanism that controls converted monomer concentration such that premature termination or secondary growth processes are prevented.
Grain boundary engineering, by electrodeposition and demoulding of elemental metal from a van der Waals gap, gives rise to nanosheets with high electrical anisotropy.
Inspired by pharmaceutical capsules, an extended-release shell to regulate catalyst surface reconstruction is developed, generating highly active sites and leading to enhanced CO2 electroreduction performance.
Two catalysts working together under light irradiation selectively dehydrogenate proteinogenic amino acids to yield intermediates that can be diversified into non-canonical amino acids.
Supramolecular peptide complexes with interlocking heterochiral linkers showcase a route for self-assembled nanostructures with exceptional mechanical stability.
Anisotropic gels made from supramolecular nanofibres are formed from mechanical or magnetic forces applied with orchestrated enzymatically-triggered pH changes.
Enantioenriched alkyl–alkyl bonds are produced from abundant alkenes in one step via Ni-catalysed asymmetric cross-hydrodimerization. This technique overcomes the reactivity and selectivity challenges associated with coupling between two similar nucleophiles.
Aryl thianthrenium salts participate in Suzuki–Miyaura cross-coupling reactions with boronic acids. Notably, the reactions occur at low pH, facilitating the use of base-sensitive boronic acids or Lewis basic substrates.
Diarylated cyclooctenes encode head-to-head styrene dyads that form precision polyolefins after ring-opening metathesis polymerization and hydrogenation.
Iron-catalysed C–H activation enables the aza-annulation of extended π-conjugated systems to access N-doped polycyclic aromatics with outstanding optoelectronic properties.
Strategic modification of molecular catalysts has led to efficient CO2 reduction in strong acid while suppressing the competing hydrogen evolution reaction.
The iterative operation of certain polyketide synthase modules is demonstrated in vitro using a combination of protein biochemistry, synthesis of biosynthetic intermediates, and mass spectrometric analysis.
Enantioselective hydrogenation is a stalwart reaction in synthetic chemistry. Now, hydrogenation of tetrasubstituted 1,2-dihydronaphthalene esters gives access to more than 30 cyclolignan natural products.
Amine–borane adducts activate alkyl halides via halogen-atom transfer through boryl radical intermediates, enabling the formation of C(sp2)–C(sp3) bonds using either organometallic reagents or organic halides.