04.02.2013 Views

handbook of carbon, graphite, diamond and fullerenes

handbook of carbon, graphite, diamond and fullerenes

handbook of carbon, graphite, diamond and fullerenes

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

360 Carbon, Graphite, Diamond, <strong>and</strong> Fullerenes<br />

2.2 Characteristics <strong>of</strong> the Fullerene Molecules<br />

General Characteristics. The fullerene structure is unique in the<br />

sense that the molecules are edgeless, chargeless, <strong>and</strong> have no boundaries,<br />

no dangling bonds, <strong>and</strong> no unpaired electron. These characteristics<br />

set the <strong>fullerenes</strong> apart from other crystalline structures such as <strong>graphite</strong> or<br />

<strong>diamond</strong> which have edges with dangling bonds <strong>and</strong> electrical charges.! 2 '<br />

Such features allow these molecules, <strong>and</strong> particularly the C^ which is<br />

the most symmetrical, to spin with essentially no restraint at a very high<br />

rate.! 3 '<br />

The Fullerene Family. Many fullerene structures are theoretically<br />

possible, some with hundreds <strong>of</strong> atoms. Five have been unambiguously<br />

identified <strong>and</strong> structurally characterized so far: the C^, C^, G^, C^, <strong>and</strong><br />

At one end <strong>of</strong> the fullerene family is the C20. the simplest<br />

structure, which is composed <strong>of</strong> twelve pentagons with<br />

no hexagon <strong>and</strong> with a pyramidization angle <strong>of</strong> 18°. All<br />

its atoms would have the sp 3 configuration but it is<br />

thermodynamically unstable.! 8 '<br />

The first stable fullerene <strong>and</strong> the first to be discovered is<br />

the CgQ. It is the dominant molecule with sixty <strong>carbon</strong><br />

atoms arranged so that they form twenty hexagons, in<br />

addition to the necessary twelve pentagons, giving it the<br />

appearance <strong>of</strong> a soccer ball (known as a football outside<br />

the U.S.A. <strong>and</strong> U.K.). Each hexagon is connected to<br />

alternating pentagon <strong>and</strong> hexagon, <strong>and</strong> each <strong>carbon</strong><br />

atom is shared by one pentagon <strong>and</strong> two hexagons. Its<br />

hybridization is partially sp 3 <strong>and</strong> partially sp 2 , with a<br />

pyramidization angle <strong>of</strong> 11.6°. It is shown schematically<br />

in Fig. 15.4. The C^ has a calculated diameter <strong>of</strong> 0.710<br />

+/- 0.007 nm. It is intensely purple in apolar solvents.' 7 '! 8 '<br />

The higher <strong>fullerenes</strong> are shown schematically in Fig.<br />

1 5.S.! 7 ' The Cy0 is the second most prominent fullerene.<br />

It has a rugby-ball appearance <strong>and</strong> is has a deep orangered<br />

color in solution. The Cj6 is c/7/ra/with a structure<br />

consisting <strong>of</strong> a spiraling arrangement <strong>of</strong> pentagons <strong>and</strong><br />

hexagons.' 91 it has a bright yellow-green color in solution

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!