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Covalent chemistry of single walled nanotubes(SWNTs).

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Solubility increases to 1mg/ml after functionalization. ... Amidation of COCl by amine such as octadecylamine(ODA) Source: J. Mater. Chem.2002,1952 ... – PowerPoint PPT presentation

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Title: Covalent chemistry of single walled nanotubes(SWNTs).


1
Covalent chemistry of single walled nanotubes
Krishna Prasad Bastola,
Graduate Student, Chemistry Department
Oklahoma State University
2
  • SWNTs
  • High metallic conductivity.
  • High tensile strength, high elasticity.
  • High chemical and thermal stability.
  • Ability to absorb gas molecules as nano
    capillaries.

3
Other applications of SWNTs need chemical
modification
  • Two types of chemical modification
  • non covalent interaction
  • Covalent Interaction (functionalization of
    SWNTs)

4
Solubility of SWNT as such in different solvents
is about 5mg/50 ml. Solubility increases to
1mg/ml after functionalization. Attachment of
desired moieties in SWNTs possible only in
solution.
AFM of functionalized tube
AFM of unfunctionalized tube
SourceTexas institutes for intelligent bio
nanomaterials, NASA
5
Steps involved in functionalization
Introduction of COOH groups Changing COOH to
COCl Amidation of COCl by amine such as
octadecylamine(ODA)
Source J. Mater. Chem.2002,1952
6
Schematics of functionalization route.
7
Characterization of functionalized SWNTs
  • No standard techniques yet.
  • ATR good tools to identify functional groups (FG)
  • NMR has some application but to interpret spectra
    is difficult
  • Raman spectroscopy is useful specially for the
    (FG) in
  • side wall of SWNT
  • TGA ( thermal gravimetric analysis) used
    extensively as the FG are labile.
  • SEM,AFM, TEM, and STM microscopy's are also very
    useful.

8
  • Potential applications of functional SWNTs.
  • Fluorinated SWNTs as cathode in lithium
    electrochemical cell.
  • Polyethyleneimine-SWNT in neuronal growth
  • Functionalized SWNT as CFM tips

9
References 1.A to Z of nanotechnology. 2 A.
David and et al. chem. soc. rev. 2006, 35, 637.
3. P. AVOURIS Acc. Chem. Res. 2002, 35,
1026. 4. R. Saito and et al. imperial college
London 1998. 5.C. Dekker phys. Today 1999,
52(5),22. 6. T. Odom and et al. J. Phys. Chem.B
2000, 104, 2794. 7.S. Banerjee Adv. Mater. 2005,
17(1), 17-29 8. T. Oku I. Narita Physica B
Condensed Matter 2002, 323(1-4), 216. 9. S.
Niyogi and et al. Acc. Chem. Res. 2002, 35(12),
1105. 10. L. Jeffrey J. Mater. Chem. 2002, 12,
1952-58. 11. A. Hirsch Angew. Chem. Int. Ed.
2002, 41, 1853. 12. J. Liu and et al. Science
1998, 280, 1253-1256. 13. A. G. Rinzler and et
al. Apply. Phys. A 1998, 67, 29-37. 14. J. Liu
and et al. Science 1998, 280, 1253. 15. M. A.
Hamon and et al. Adv. Mater 1999, 11, 834. 16.
L. Qu and et al. J. chem. phys. 2002, 117,
8089. 17. Y. P. Sun and et al. Chem. Mater.
2201, 13, 2864. 18. B. Li and et al. Chem.
Lett. 2001, 598. 19. B. R. Azamian and et al.
Chem. Commun. 2002, 366. 20. S.Ravindran and et
al. Nano Lett. 2003, 3, 447 21. S. Banerjee, S.
S. Wong J. Am. Chem. Soc. 2002, 124, 8940. 22.
S. Banerjee, S. S. Wong Nano Lett. 2002, 2, 49
10
  • Thank You very
    much
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