Progress and challenges for the bottom-up synthesis of carbon nanotubes with discrete chirality

Chemical Physics Letters

Volumn 494, Issue 1-3, 2010, Pages 1-7

  Jasti, Ramesh ^a   Bertozzi, Carolyn R ^b  

^a BOSTON UNIVERSITY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATOMIC LEVELS; ORGANIC SYNTHESIS; PROMISING MATERIALS; STRUCTURAL CONTROL; SYNTHETIC METHODS; WELL-DEFINED STRUCTURES;

STEREOCHEMISTRY; STRUCTURAL DYNAMICS;

CARBON NANOTUBES;

EID: 77955922606     PISSN: 00092614     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cplett.2010.04.067     Document Type: Article

References (50)

1. S. Iijima Nature 354 1991 56
2. N. Hamada, S. Sawada, and A. Oshiyama Phys. Rev. Lett. 68 1992 1579
3. T.W. Odom, J. Huang, and C.M. Lieber Ann. NY Acad. Sci. 960 2002 203
4. H. Dai Acc. Chem. Res. 35 2002 1035
5. X. Liu, C. Lee, S. Han, C. Li, C. Zhou, in: M.A. Reed, T. Lee (Eds.), Molecular Nanoelectronics, 2003, p. 179.
6. M. Terrones Int. Mat. Rev. 49 2004 325
7. This number was estimated based on a SciFinder Scholar search.
8. X. Wang Nano Lett. 9 2009 3137
9. M. Yu, O. Lourie, M.J. Dyer, K. Moloni, T.F. Kelly, and R.S. Ruoff Science 287 2000 637
10. Z.K. Tang Science 292 2001 2462
11. E. Joselevich ChemPhysChem 5 2004 619
12. J.A. Misewich, R. Martel, Ph. Avouris, J.C. Tsang, S. Heinze, and J. Tersoff Science 300 2003 783
13. W.J. Kim, M.L. Usrey, and M.S. Strano Chem. Mater. 19 2007 1571
14. M.S. Arnold, S.I. Stupp, and M.C. Hersam Nano Lett. 5 2005 713
15. M.C. Hersam Nat. Nanotechnol. 3 2008 387
16. M.S. Dresselhaus, G. Dresselhaus, P. Avouris (Eds.), Carbon Nanotubes: Synthesis, Structure, Properties and Applications, vol. 80, Springer-Verlag, Heidelberg, Germany, 2001 (Top. Appl. Phys.).
17. Z. Yao, H.W.C. Postma, L. Balents, and C. Dekker Nature 402 1999 273
18. T. Guo, P. Nikolaev, A. Thess, D.T. Colbert, and R.E. Smalley Chem. Phys. Lett. 243 1995 49
19. M. José-Yamacán, M. Miki-Yoshida, L. Rendón, and J.G. Santiesteban Appl. Phys. Lett. 62 1993 657
20. A.R. Harutyunyan Science 326 2009 116
21. L. Qu, F. Du, and L. Dai Nano Lett. 8 2008 2682
22. V.C. Parekh, and P.C. Guha J. Indian Chem. Soc. 11 1934 95
23. R. Friederich, M. Nieger, and F. Vögtle Chem. Ber. 126 1993 1723
24. M. Srinivasan, S. Sankararaman, H. Hopf, and B. Varghese Eur. J. Org. Chem. 2003 660
25. R. Jasti, J. Bhattacharjee, J.B. Neaton, and C.R. Bertozzi J. Am. Chem. Soc. 130 2008 17646
26. The direct product of this reaction is the diol, which is subsequently converted to the methyl ether 5.
27. F. Alonso, and M. Yus Tetrahedron 47 1991 7471
28. N. Miyaura, and A. Suzuki Chem. Rev. 95 1995 2457
29. The one relevant example in the literature produces a mixture of para- and meta-substituted aryl rings: G.W. Morrow, B. Schwind, Synth. Commun. 25 (1995) 269.
30. F. Alonso, and M. Yus Tetrahedron 48 1992 2709
31. N.I. Nijegorodov, W.S. Downey, and M.B. Danailov Spectrochim. Acta Part A 56 2000 783
32. D.R. Salahub, M. Castro, and E.I. Proynov NATO ASI Ser. B: Phys. 318 1994 411
33. R.O. Jones, and O. Gunnarsson Rev. Mod. Phys. 61 1989 689
34. A. Hellman, B. Razaznejad, and B.I. Lundqvist J. Chem. Phys. 120 2004 4593
35. These trends in optical data were further explored in the following article: B.M. Wong, J. Phys. Chem. C 113 (2009) 21921.
36. H. Takaba, H. Omachi, Y. Yamamoto, J. Bouffard, and K. Itami Angew. Chem. Int. Ed. 48 2009 6112
37. S. Yamago, Y. Watanabe, and T. Iwamoto Angew. Chem. Int. Ed. 49 2010 757
38. U. Girreser, D. Giuffrida, F.H. Kohnke, J.P. Mathias, D. Philp, and J.F. Stoddart Pur. Appl. Chem. 65 1993 119
39. T.J. Hill, R.K. Hughes, and L.T. Scott Tetrahedron 64 2008 11360
40. B.D. Steinberg, and L.T. Scott Angew. Chem. Int. Ed. 48 2009 5400
41. Y.H. Wang Nano Lett. 5 2005 997
42. R.E. Smalley J. Am. Chem. Soc. 128 2006 15824
43. D. Ogrin J. Phys. Chem. C 111 2007 17804
44. J.A. Berson Tetrahedron 48 1992 3
45. K.C. Nicolaou, S.A. Snyder, T. Montagnon, and G. Vassilikogiannakis Angew. Chem. Int. Ed. 41 2002 1668
46. Acetylene equivalents are masked versions of acetylene that are more reactive. For example, see: R.V. Williams, K. Chauhan, V.R. Gadgil, J. Chem. Soc. (1994) 1739.
47. E. Clar, and M. Zander J. Chem. Soc. 1957 4616
48. E.H. Fort, P.M. Donovan, and L.T. Scott J. Am. Chem. Soc. 131 2009 16006
49. C.C. Price Org. React. 3 1946 1
50. B.A. Arndtsen, R.G. Bergman, T.A. Mobley, and T.H. Peterson Acc. Chem. Res. 28 1995 154