Covalent functionalization of alkyne-decorated SWNTs with well-defined, azide-terminatedpolystyrene polymers was accomplished by the Cu(I)-catalyzed [3 + 2] Huisgen cycloaddition. This reactionwas found to be extremely efficient in producing organosoluble polymer-nanotube conjugates, even atrelatively low reaction temperatures (60
![](/images/entities/deg.gif)
C) and short reaction times (24 h). The reaction was found to bemost effective when a CuI catalyst was employed in the presence of 1,8-diaza
bicyclo[5.4.0]undec-7-eneas an additive. IR spectroscopy was utilized to follow the introduction and consumption of alkyne groupson the SWNTs, and Raman spectroscopy evidenced the conversion of a high proportion of sp
2 carbons tosp
3 hybridization during alkyne introduction. Thermogravimetric analysis indicated that the polymer-functionalized SWNTs consisted of 45% polymer, amounting to approximately one polymer chain for every200-700 carbons of the nanotubes, depending on polymer molecular weight. Transmission electronmicroscopy and atomic force microscopy were utilized to image polymer-functionalized SWNTs, showingrelatively uniform polymer coatings present on the surface of individual, debundled nanotubes.