0000000000393950
AUTHOR
Heli Leinonen
New nitrene functionalizations onto sidewalls of carbon nanotubes and their spectroscopic analysis
Abstract The reactivity of p -toluenesulfonyl, methylsulfonyl and trimethylsilyl nitrene, derived from the corresponding azides, was studied towards single-walled carbon nanotubes (SWCNT) prepared by electric arc or HiPCO (High-pressure CO conversion) methods. The functionalized SWCNTs were analyzed by Raman, IR, and VIS/NIR spectroscopy. The spectroscopic results indicated that covalent modification of the SWCNTs was successful. While the IR measurements gave evidence of successful reaction in all studied cases, the Raman measurements indicated differences in the reactivity of the two tube types and between different nitrenes. VIS/NIR spectrum was measured for reaction with p -toluenesulfo…
Water-soluble carbon nanotubes through sugar azide functionalization
In this work we report a covalent functionalization of pristine single-walled carbon nanotubes (SWCNTs) directly with three sugar azides, 2,3,4,6-tetra-O-acetyl-β-d-glucopyranosyl, 2,3,4,6-tetra-O-acetyl-β-d-galactopyranosyl or 2,3,4,6-tetra-O-acetyl-β-d-mannopyranosyl azide. Microwave-assisted functionalization was carried out for SWCNTs prepared with the HiPCO method. The as-prepared, new type of sugar-functionalized SWCNTs were analyzed by Raman and IR spectroscopy. Deacetylation of the functionalized tubes by sodium methoxide yielded nitrogen-linked, sugar-functionalized carbon nanotubes (CNTs) that formed stable dispersions in water. Reactivity of the sugar azides towards SWCNTs was es…