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By Katharina Kaiser, Fabian Schulz, and Leo Gross (IBM Research - Zurich); Lorel M. Scriven, Przemyslaw Gawel and Harry L. Anderson (Oxford University)

Making and imaging a ring of 18 carbon atoms for the first time

Carbon, one of the most abundant elements in the universe, can exist in different forms - called allotropes - giving it completely different properties from colour to shape to hardness. For example, in a diamond every carbon atom is bonded to four neighbouring carbons, whereas in graphite, every carbon atom is bonded to three neighbouring carbons.

While these are well studied forms of carbon, there are lesser-known forms and one in particular has been elusive – cyclocarbons, where the carbon atoms have only two neighbours, arranged in the shape of a ring. Discussed for many years, their structure was unknown, and two possibilities were debated, either with all the bonds in the ring of the same length or with alternating shorter and longer bonds. Adding to the drama, evidence for their existence was published in the gas phase, but due to their high reactivity, they could not be isolated and characterised – that is until now.

Based on our previous successes in imaging molecules with atomic force microscopy (AFM) and creating molecules by atom manipulation, scientists from the University of Oxford's Department of Chemistry and IBM Research attempted to find the answer to this debate. Our goal was to synthesise, stabilise and characterise cyclocarbon.

And for the first time, we have succeeded in stabilising and imaging a ring of 18 carbon atoms.

Our approach was to generate cyclocarbon by atom manipulation on an inert surface at low temperatures (5 K) and to investigate it with high-resolution AFM. We started the collaboration between the groups of Oxford and IBM three years ago with this goal. Initially, we focused on linear segments of two-fold coordinated carbons, exploring possible routes for creating such carbon-rich materials by atom manipulation. We triggered chemical reactions by applying voltage pulses with the tip of the atomic force microscope. We found that such segments could be formed on a copper substrate covered by a very thin layer of table salt. Because the salt layer is chemically very inert, the reactive molecules did not form covalent bonds to it.

After the successful creation of the linear carbon segments, we attempted to create cyclocarbon on the same surface. To this end, the Oxford group synthesised a precursor to cyclo[18]carbon that is a ring of 18 carbon atoms.

Future applications are suggested by the fact that we could fuse cyclocarbons and/or cyclic carbonoxides by atom manipulation. This possibility of forming larger carbon rich structures by fusing molecules with atom manipulation opens the way to create more sophisticated carbon-rich molecules and new carbon allotropes. Eventually, custom-made molecular structures might be used as elements for molecular electronics, based on single electron transfer.