Chemical Attachment of Organic Functional Groups to Single-walled Carbon Nanotube Material
- 1 September 1998
- journal article
- Published by Springer Nature in Journal of Materials Research
- Vol. 13 (9), 2423-2431
- https://doi.org/10.1557/jmr.1998.0337
Abstract
We have subjected single-walled carbon nanotube materials (SWNTM's) to a variety of organic functionalization reactions. These reactions include radioactive photolabeling studies using diradical and nitrene sources, and treatment with dichlorocarbene and Birch reduction conditions. All of the reactions provide evidence for chemical attachment to the SWNTM's, but because of the impure nature of the staring materials, we are unable to ascertain the site of reaction. In the case of dichlorocarbene we are able to show the presence of chlorine in the SWNT bundles, but as a result of the large amount of amorphous carbon that is attached to the tube walls, we cannot distinguish between attachment of dichlorocarbene to the walls of the SWNT's and reaction with the amorphous carbon.Keywords
This publication has 16 references indexed in Scilit:
- Benzyne Adds Across a Closed 5−6 Ring Fusion in C70: Evidence for Bond Delocalization in FullerenesJournal of the American Chemical Society, 1998
- Diameter-Selective Raman Scattering from Vibrational Modes in Carbon NanotubesScience, 1997
- Covalent Fullerene ChemistryScience, 1996
- Photochemical and Thermal Reactions of C60 with N-Succinimidyl 4-Azido-2,3,5,6-tetrafluorobenzoate: A New Method for Functionalization of C60The Journal of Organic Chemistry, 1994
- The Chemistry of the FullerenesPublished by Wiley ,1994
- C61Cl2. Synthesis and characterization of dichlorocarbene adducts of C60Tetrahedron Letters, 1993
- Chemistry of the Fullerenes: The Manifestation of Strain in a Class of Continuous Aromatic MoleculesScience, 1993
- The chemical properties of buckminsterfullerene (C60) and the birth and infancy of fulleroidsAccounts of Chemical Research, 1992
- Efficient production of C60 (buckminsterfullerene), C60H36, and the solvated buckide ionThe Journal of Physical Chemistry, 1990
- Phenyl(trihalomethyl)mercury compounds. Exceptionally versatile dihalocarbene precursorsAccounts of Chemical Research, 1972