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.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.