Covalent amino-functionalisation of single-wall carbon nanotubes
- 11 July 2005
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry
- Vol. 15 (32), 3334-3339
- https://doi.org/10.1039/b504282h
Abstract
Chemical transformation of single-wall carbon nanotubes (SWNT), edge-terminated with carboxylic groups, to SWNT species with amino groups directly attached to the tube open ends has been performed. Different synthetic approaches have been investigated. The reaction products were characterised by FTIR, Raman spectroscopy, XPS and SEM.Keywords
This publication has 48 references indexed in Scilit:
- Correlation of the chemical properties of carbon nanotubes with their atomic and electronic structuresPhysics of the Solid State, 2004
- Computational Studies of Carbon Nanotube–Hydrocarbon Bond Strengths at Nanotube Ends: Effect of Link Heteroatom and Hydrocarbon StructureChemistry – A European Journal, 2004
- Electronic Properties of Carbon Nanotubes with Covalent Sidewall FunctionalizationThe Journal of Physical Chemistry B, 2004
- Sidewall Carboxylic Acid Functionalization of Single-Walled Carbon NanotubesJournal of the American Chemical Society, 2003
- Functionalization of Single-Walled Carbon Nanotubes with (R-)Oxycarbonyl NitrenesJournal of the American Chemical Society, 2003
- Rational Chemical Strategies for Carbon Nanotube FunctionalizationChemistry – A European Journal, 2003
- Theoretical Analysis of Ether-Group Derivatization at Carbon Nanotube EndsNano Letters, 2003
- Functionalization of carbon nanotubes through the chemical binding of atoms and moleculesPhysical Review B, 2003
- Current-voltage characteristics of carbon nanotubes with substitutional nitrogenPhysical Review B, 2002
- Comparative analysis of various methods of purification of single-walled carbon nanotubesPhysics of the Solid State, 2002