ERROR 1
ERROR 1
ERROR 2
ERROR 2
ERROR 2
ERROR 2
ERROR 2
Password and Confirm password must match.
If you have an ACS member number, please enter it here so we can link this account to your membership. (optional)
ERROR 2
ACS values your privacy. By submitting your information, you are gaining access to C&EN and subscribing to our weekly newsletter. We use the information you provide to make your reading experience better, and we will never sell your data to third party members.
Decades before nanoscientists zapped graphite with an electrical discharge to make the first carbon nanotubes, synthetic chemists were trying to craft similar, smaller structures in their reaction flasks. But the belt-shaped compounds these chemists were trying to create entirely from fused benzene rings were tough to come by. Chemists observed one such structure fleetingly via mass spectrometry a decade ago, but no one has been able to synthesize and isolate enough of these carbon nanobelts for further study—until now. Kenichiro Itami, Yasutomo Segawa, and coworkers at Nagoya University managed to fashion a nanobelt out of 12 aromatic rings (shown) via a series of successive Wittig reactions followed by a nickel-catalyzed aryl-aryl coupling reaction (Science 2017, DOI: 10.1126/science.aam8158). Although they synthesized the nanobelt in only 0.2% overall yield, the Nagoya researchers made enough of it to get crystals for X-ray analysis. The crystal structure reveals that the bonds at the nanobelt’s equator have benzene-like bond lengths of about 1.4 Å, while the remaining bonds have single- and double-bond characters. The researchers believe the nanobelts could serve as seed molecules for making structurally well-defined carbon nanotubes.
Join the conversation
Contact the reporter
Submit a Letter to the Editor for publication
Engage with us on X