...somewhat dangerous, environmentally dangerous and perhaps even quite toxic???
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But carbon nanotubes are also inert and chemically stable, which has made it difficult for chemists to create nanotube derivatives -- tubes decorated with extra molecules that act as chemical "handles" for further manipulation. Most processes that laboratory researchers have used to create nanotube derivatives are impractical on a macro scale because they involve the use of extremely high temperatures, high pressures or other techniques that are difficult to reproduce in a production setting.
Fluorine, which is often shunned by chemists because of its highly reactive nature, has proven to be very useful as an alternative means of creating nanotube derivatives, precisely for that reason. The addition of fluorine opens the door to subsequent chemical reactions, giving chemists the ability to attach other types of molecules to nanotubes.
So far, Margrave and his colleagues have used this process to create dozens of "designer" nanotube derivatives. These include hydrotubes, which contain hydrogen in an activated form; hexyl nanotubes, methoxy nanotubes, amido nanotubes, and other varieties containing organic side chains; polymers similar to nylon; and hydrogen-bonded nylon analogs. Unlike pure carbon nanotubes, all these derivatives are soluble in traditional organic solvents.
<more>
<link>
http://www.sciencedaily.com/releases/2002/04/020412081030.htm