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1 Covalent chemistry of single walled nanotubes Krishna Prasad Bastola, Graduate Student, Chemistry Department Oklahoma State University.

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Presentation on theme: "1 Covalent chemistry of single walled nanotubes Krishna Prasad Bastola, Graduate Student, Chemistry Department Oklahoma State University."— Presentation transcript:

1 1 Covalent chemistry of single walled nanotubes Krishna Prasad Bastola, Graduate Student, Chemistry Department Oklahoma State University

2 2 SWNTs:  High metallic conductivity.  High tensile strength, high elasticity.  High chemical and thermal stability.  Ability to absorb gas molecules as nano capillaries.

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

4 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 Source:Texas institutes for intelligent bio nanomaterials, NASA

5 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 6 Schematics of functionalization route.

7 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 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 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 10 Thank You very much


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