The latest news from academia, regulators
research labs and other things of interest
Posted: Aug 29, 2014
Separating the buckybowl twins
(Nanowerk News) Corannulene is a bowl-shaped polycyclic aromatic hydrocarbon with a skeleton of bonded carbon atoms equivalent to a segment of the buckminsterfullerene or ‘buckyball’—a soccer-ball-like structure of 60 carbon atoms. This similarity to the buckyball has led to corannulene being dubbed the ‘buckybowl’. Chemists are interested in the chemical potential of corannulenes as catalysts and in nanotechnology applications, but exploring the potential of these molecules is complicated because they invert rapidly between their mirror-image or ‘chiral’ forms (Fig. 1).
The achievement marks an important step toward being able to work with and perhaps isolate the individual chiral forms to explore their possible uses. “For example, if we can desymmetrize and produce corannulene complexes with transition metals, it might be possible to develop asymmetric catalysts with unique characteristics due to the bowl-shaped structure of corannulene,” explains Miyajima.
The key to biasing the inversion process was to add different chemical groups that can interact through intramolecular hydrogen bonding, whereby hydrogen atoms with a slight positive charge are attracted to other atoms with a slight negative charge. These forces of attraction within each molecule stabilize the corannulene bowl in one of its chiral versions by establishing a thermodynamic preference for the chiral form that allows all the interacting units to be hydrogen bonded at the same time.
Although a significant achievement, this desymmetrization of corannulene equilibrium is only partial. The conversion between the two forms is not stopped completely but is merely slowed down and made to favor one form over the other. The next challenge for the research team is to find modifications that can stop the conversion completely and perhaps allow just one of the stabilized bowl structures to be purified and used in the complete absence of its inverted partner.
There are numerous incentives for achieving chiral purity of corannulenes beyond catalyst applications. “Other researchers are working on utilizing corannulenes for making carbon nanotubes,” says Miyajima, “and so our research may contribute to the synthesis of chirality-selective nanotubes.” As chiral asymmetry is critical for many precise chemical reactions, the selective enrichment of nanotubes favoring one chirality could open new possibilities in nanotechnology.