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Quantum tunnelling can at times be the cause of kinetic isotope effects, and in these cases conventional wisdom has been that molecules with isotopes of larger mass will react more slowly. New calculations, however, predict that sometimes the reverse should be true.
An enzyme that is unusually tolerant of a truly broad range of substrates can catalyse aldol-type chemistry on sugars in which the various hydroxyl groups are protected. The new methodology combines some of the most important advantages of enzyme and small-molecule catalysis.
Embedding platinum nanoparticles in a polymer matrix produces a system that reacts like a homogeneous catalyst, but provides the stability and separation advantages of a heterogeneous one.
Although it may seem counter-intuitive, the attraction between positively charged radical ions offers a new approach to driving controlled motion in molecular machines.
Small-molecule enzyme-inhibitors often display insufficient affinity and selectivity for their targets causing unwanted side effects when used as drugs. Molecularly imprinted polymers prepared using the enzyme as a template could offer a solution.
Synthetic procedures for making nanoparticles often result in samples that contain a range of different particle sizes. By using hollow self-assembled metal–organic spheres as templates, however, it is possible to make silica nanoparticles with uniform shapes and sizes in a precisely controlled fashion.
Among the wide variety of synthetic processes that chemists have developed, only a few can be carried out under physiological conditions. A condensation reaction that is controlled by the constituents of cells has led to the formation of nanostructures within living cells.
Electrically tunable materials are used to construct switches and memory devices. Applying an electric field within a specific temperature range to cyanometallate complexes triggers their charge-transfer phase transition, altering their optical and magnetic properties.