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Open-shell PAHs gain attention of A*STAR researchers

Posted: 26 Apr 2013 ?? ?Print Version ?Bookmark and Share

Keywords:polycyclic aromatic hydrocarbon? open-shell PAH? benzene?

A team of researchers from A*STAR Institute of Materials Research and Engineering in Singapore has been focusing on a class of organic materials known as open-shell polycyclic aromatic hydrocarbons (PAHs) that paves the way for more flexible and lightweight components. The molecules consist of interlocked, benzene-like rings and contain unpaired electrons, or 'free-radical' centres that can be leveraged by manufacturers to achieve cost savings, the researchers added.

Interactions between the radical centres and aromatic electrons make these compounds extremely responsive to light- and electron-based stimuli. Unfortunately, these same radical electrons can quickly degrade PAH chemical structures, rendering them unusable.

Jishan Wu from the A*STAR and an international team of co-workers have devised a stabilisation strategy that promises to make open-shell PAHs even more practical. Through clever modification of a prototypical compound known as Chichibabin's hydrocarbon, the team has produced two types of PAHs that retain active radical centres for unprecedented amounts of time.

Chichibabin's hydrocarbon has a sextet of aromatic rings that thermodynamically stabilise radical centres. However, it also has a strong chemical affinity for oxygen atoms and tends to polymerise in their presence. To resolve this issue, Wu and co-workers used a process known as benzannulation to add four additional aromatic benzene rings to the PAH framework. They anticipated this design could enhance thermodynamic stability and block kinetic polymerisation interactions.

When the researchers chemically excited the tetrabenzo-Chichibabin's hydrocarbon to an open-shell system, they saw that the radical centres remained active for an unusually long timetwo full daysbefore returning to the low-energy ground state. Using a combination of high-resolution spectroscopy and theoretical calculations, the team discovered the radical's benzene rings were oriented at right angles to one another, while the ground-state compound had a relatively flat, butterfly-like ring layout. The large energy barrier between these two geometries kept the radical active. "This opens the possibility of accessing each form of the PAH molecule and understanding its physical properties," noted Wu.

The researchers also modified the tetrabenzo-Chichibabin's hydrocarbon with aromatic fluorenyl rings that have well-known radical stabilising effects. In fact, the stabilising capacity of this compound proved so strong that the open-shell radical became the lowest-energy state, and the molecule remained stable for months under ambient air and light conditions.

Experiments revealed these new open-shell PAHs to have valuable properties including enhanced two-photon absorption, a strong magnetic response and multiple redox states. Wu notes that these findings may lead to the development of better photodynamic therapies and magnetic imaging techniques in the future.





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