Synthesis of Water-Soluble PEGylated Single-Walled Carbon Nanotubes
Source abstract
Abstract
Carbon nanotube salts prepared by treating single-wall carbon nanotubes (SWNTs) with lithium in liquid ammonia react with ω-bromocarboxylic acids to yield sidewall-derivatized SWNTs. These can be reacted with amine-terminated polyethyleneglycol (PEG) chains (e.g., H 2 N−mPEG−OMe, MW = 5000 Da) to yield water-soluble PEGylated SWNTs. Short nanotubes (average length ∼ 60 nm) functionalized by PEGylation of the carboxylic acid groups at the end of the nanotubes exhibit greater solubility in water than the longer (average length ∼ 300 nm) sidewall-PEGylated pristine nanotubes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Carbon Nanotubes in Composites · Graphene research and applications · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and The Richard E. Smalley Institute for Nanoscale Science and Technology, Rice University, Houston, Texas 77005, and Department of Chemical Engineering, University of Cambridge, Pembroke Street, Cambridge CB2 3RA, UK
References (38)
Show source-provided references
1. Bekyarova E. · J. Biomed. Nanotechnol. · 2005 · 1 · 310.1166/jbn.2005.004 ↗
2. Kam N. W. S. · Proc. Natl. Acad. Sci. U.S.A. · 2005 · 102 · 1160010.1073/pnas.0502680102 ↗
3. Kam N. W. S. · J. Am. Chem. Soc. · 2005 · 127 · 1249210.1021/ja053962k ↗
4. Chen R. J. · J. Am. Chem. Soc. · 2001 · 123 · 383810.1021/ja010172b ↗
5. Ni Y. · J. Nanosci. Nanotechnol. · 2005 · 5 · 170710.1166/jnn.2005.189 ↗
6. Wong S. S. · Nature · 1998 · 394 · 5210.1038/27873 ↗
7. Dujardin E. · J. Adv. Mater. · 1998 · 10 · 147210.1002/(SICI)1521-4095(199812)10:17<1472::AID-ADMA1472>3.0.CO;2-R ↗
8. Niyogi S. · J. Am. Chem. Soc. · 2001 · 123 · 73310.1021/ja0024439 ↗
9. Mawhinney D. B. · J. Am. Chem. Soc. · 2000 · 122 · 23810.1021/ja994094s ↗
10. Riggs J. E. · J. Am. Chem. Soc. · 2000 · 122 · 587910.1021/ja9942282 ↗
11. Tang B. Z. · Macromolecules · 1999 · 32 · 256910.1021/ma981825k ↗
12. Jin Z. · Chem. Phys. Lett. · 2000 · 318 · 50510.1016/S0009-2614(00)00091-9 ↗
13. Riggs J. E. · J. Phys. Chem. B · 2000 · 104 · 707110.1021/jp0011591 ↗
14. Czerw R. · Nano Lett. · 2001 · 8 · 42310.1021/nl015548y ↗
15. Star A. · Angew. Chem., Int. Ed. · 2001 · 40 · 172110.1002/1521-3773(20010504)40:9<1721::AID-ANIE17210>3.0.CO;2-F ↗
16. Sano M. · Langmuir · 2001 · 17 · 512510.1021/la010126p ↗
17. Dyke C. A. · J. Phys. Chem. A · 2004 · 108 · 1115110.1021/jp046274g ↗
18. Chen J. · Science · 1998 · 282 · 9510.1126/science.282.5386.95 ↗
19. Hamon M. A. · Adv. Mater. · 1999 · 11 · 83410.1002/(SICI)1521-4095(199907)11:10<834::AID-ADMA834>3.0.CO;2-R ↗
20. Fernando S. · Langmuir · 2004 · 20 · 477710.1021/la036217z ↗
21. Lin Y. · J. Phys. Chem. B · 2002 · 106 · 129410.1021/jp013501v ↗
22. Huang W. · Nano Lett. · 2003 · 3 · 56510.1021/nl0340834 ↗
23. Fu K. · Nano Lett. · 2001 · 8 · 43910.1021/nl010040g ↗
24. Sun Y.-P. · Acc. Chem. Res. · 2002 · 35 · 109610.1021/ar010160v ↗
25. Niyogi S. · Acc. Chem. Res. · 2002 · 35 · 110510.1021/ar010155r ↗
26. Banerjee S. · Nano Lett. · 2002 · 2 · 4910.1021/nl010070j ↗
27. Georgakilas V. · J. Am. Chem. Soc. · 2002 · 124 · 76010.1021/ja016954m ↗
28. Liang F. · Nano Lett. · 2004 · 4 · 125710.1021/nl049428c ↗
29. Chattopadhyay J. · Org. Lett. · 2005 · 7 · 406710.1021/ol050862a ↗
30. Xu Y. · Nano Lett. · 2005 · 5 · 16310.1021/nl048300s ↗
31. Ziegler K. J. · J. Am. Chem. Soc. · 2005 · 127 · 154110.1021/ja044537e ↗
32. Ziegler K. J. · Nanotechnology · 2005 · 16 · 553910.1088/0957-4484/16/7/031 ↗
33. Banerjee S. · J. Am. Chem. Soc. · 2002 · 124 · 849010.1021/ja026487o ↗
34. Chen J. · J. Phys. Chem. B · 2001 · 105 · 252510.1021/jp002596i ↗
35. Yue Z. · Polymer · 2005 · 46 · 249710.1016/j.polymer.2004.09.041 ↗
36. Pompeo F. · Nano Lett. · 2002 · 2 · 36910.1021/nl015680y ↗
37. Zeng L. · Nano Lett. · 2005 · 5 · 200110.1021/nl0514994 ↗
38. Chen Z. · J. Am. Chem. Soc. · 2006 · 128 · 1056810.1021/ja063283p ↗