Abstract
The solubilization of oxidized carbon nanotubes has been achieved through derivatization using a functionalized organic crown ether. The resultant synthesized adduct yielded concentrations of dissolved nanotubes on the order of ∼1 g/L in water as well as in methanol, according to optical measurements. The nanotube−crown ether adduct can be readily redissolved in 10 different organic solvents at substantially high concentrations. Characterization of these solubilized adducts was performed with 1H NMR spectroscopy; 7Li NMR was also used to examine the ability of the crown ether's macrocyclic ring to bind Li+ ions. The solutions were further analyzed using UV−visible, photoluminescence, and FT-IR spectroscopies and were structurally characterized using atomic force microscopy (AFM) and transmission electron microscopy (TEM). Adduct formation likely results from a noncovalent chemical interaction between carboxylic groups on the oxidized tubes and amine moieties attached to the side chain of the crown ether derivative.
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