Abstract
We present design and synthesis of a new class of chiral figure-of-eight
carbon nanohoops by integrating [6]helicene into [7]cycloparaphenylene.
The stereogenic [6]helicene unit endows the helicene carbon nanohoop
with chiroptical properties and configurational stability typical for
higher helicenes, while the presence of radially conjugated oligo-p-phenylene
moiety provides the optoelectronic properties similar to
meta[8]cycloparaphenylene, such as emission of visible light with a high
quantum yield. We discovered that the synthesized helicene carbon
nanohoop possesses a Mobius topology in solution and confirmed this
hypothesis by variable-temperature 1H NMR spectroscopy and
DFT calculations. Our results suggest that a single helicene stereogenic
unit and high molecular strain are sufficient to induce Mobius topology in molecular nanocarbon systems.