Skip to main navigation Skip to search Skip to main content

Reversible sidewall functionalization of buckytubes

  • P. J. Boul*
  • , J. Liu
  • , E. T. Mickelson
  • , C. B. Huffman
  • , L. M. Ericson
  • , I. W. Chiang
  • , K. A. Smith
  • , D. T. Colbert
  • , R. H. Hauge
  • , J. L. Margrave
  • , R. E. Smalley
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

492 Scopus citations

Abstract

Single-wall fullerene nanotubes have been made soluble in various organic solvents, including chloroform, methylene chloride, and tetrahydrofuran by covalently attaching alkanes to their sidewalls. Sidewall-alkylated nanotubes are obtained by reacting sidewall-fluorinated nanotubes with alkyl magnesium bromides in a Grignard synthesis or by reaction with alkyllithium precursors. Covalent attachment to the sidewalls was confirmed by UV-visible spectroscopy, which is also used to show that the alkane sidewall groups can be removed by oxidizing them in air to recover pristine nanotubes.

Original languageEnglish
Pages (from-to)367-372
Number of pages6
JournalChemical Physics Letters
Volume310
Issue number3-4
DOIs
StatePublished - 3 Sep 1999
Externally publishedYes

ASJC Scopus subject areas

  • General Physics and Astronomy
  • Physical and Theoretical Chemistry

Fingerprint

Dive into the research topics of 'Reversible sidewall functionalization of buckytubes'. Together they form a unique fingerprint.

Cite this