Research Highlights
Published online: 3 March 2010 | doi:10.1038/nchina.2010.25
Material chemistry: Romance of the three pentagons
Felix Cheung
Abstract
Researchers in Xiamen have created four chlorinated fullerenes featuring triple sequentially fused pentagons
Original article citation
et al. Chlorofullerenes featuring triple sequentially fused pentagons. Nature Chem. doi:10.1038/nchem.549 (2010).Introduction

© (2010) Nature Chemistry
Fullerenes are carbon cages with pentagonal and hexagonal faces, and among them, those that violate the isolated pentagon rule (IPR; no two pentagonal faces may share an edge) are known to be highly reactive. There are several approaches to making IPR-violating fullerenes, but no-one has yet made a fullerene with triple sequentially fused pentagons (TSFPs, pictured top). Suyuan Xie, Xin Lu and co-workers at Xiamen University1 have now created four chlorinated fullerenes — all with TSFPs.
The researchers vaporized graphite in an arc-discharge reactor filled with helium and carbon tetrachloride (CCl4) gases to produce a carbon-rich soot containing chlorinated fullerenes. They then used high-performance liquid chromatography to extract various chlorinated fullerenes, namely C54Cl8, C56Cl12, C66Cl6 and C66Cl10, from the soot.
X-ray crystallography revealed the structures of the novel chlorinated fullerenes: C54Cl8 contains two sets of TSFPs; C56Cl12 (pictured bottom) contains one set of TSFPs and two sets of double fused pentagons (highlighted in red and blue, respectively); C66Cl6 and C66Cl10 both contain one set of TSFPs.
The researchers believe that there are many IPR-violating fullerenes yet to be uncovered. Nevertheless, their findings provide new clues to the formation of fullerenes.
The authors of this work are from:
State Key Laboratory for Physical Chemistry of Solid Surfaces and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China.
Reference
- Tan, Y. Z. et al. Chlorofullerenes featuring triple sequentially fused pentagons. Nature Chem. doi:10.1038/nchem.549 (2010). | Article | OpenURL
