Polyacylation of Single‐Walled Nanotubes under Friedel–Crafts Conditions: An Efficient Method for Functionalizing, Purifying, Decorating, and Linking Carbon Allotropes
Source abstract
Abstract
A new way of purifying and separating single-walled nanotubes (SWNTs, see figure) comes in the form of an efficient polyacylation using Friedel–Crafts catalysts in either nitrobenzene as a solvent or in a NaCl/AlCl3 melt. The report method provides a way for the efficient insertion not only of normal acyl chains but also of perfluorinated acyl residues or for crosslinking possibilities by using α,ω-diacyl dichlorides.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Carbon Nanotubes in Composites · Graphene research and applications · Fullerene Chemistry and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (44)
Show source-provided references
1. 10.1126/science.106092810.1126/science.1060928 ↗
2. 10.1038/318162a010.1038/318162a0 ↗
3. A. Hirsch The Chemistry of the Fullerenes Thieme Organic Chemistry Monograph Series Thieme Stuttgart Germany1994.
4. M. S. Dresselhaus G. Dresselhaus P. C. Eklund Science of Fullerenes and Carbon Nanotubes Academic San Diego CA1996.10.1016/B978-012221820-0/50003-4 ↗
5. 10.1038/354056a010.1038/354056a0 ↗
6. 10.1038/358220a010.1038/358220a0 ↗
7. 10.1016/0022-0248(76)90115-910.1016/0022-0248(76)90115-9 ↗
8. 10.1038/363603a010.1038/363603a0 ↗
9. 10.1038/363605a010.1038/363605a0 ↗
10. 10.1021/ar960168i10.1021/ar960168i ↗
11. 10.1126/science.273.5274.48310.1126/science.273.5274.483 ↗
12. 10.1016/S0009-2614(99)01029-510.1016/S0009-2614(99)01029-5 ↗
13. 10.1116/1.138072110.1116/1.1380721 ↗
14. 10.1126/science.110496210.1126/science.1104962 ↗
15. 10.1021/cr050569o10.1021/cr050569o ↗
16. 10.1002/1521-3773(20020603)41:11<1853::AID-ANIE1853>3.0.CO;2-N10.1002/1521-3773(20020603)41:11<1853::AID-ANIE1853>3.0.CO;2-N ↗
17. 10.1021/ar020146y10.1021/ar020146y ↗
18. 10.1021/ar010160v10.1021/ar010160v ↗
19. 10.1021/ar010155r10.1021/ar010155r ↗
20. 10.1021/ja981780310.1021/ja9817803 ↗
21. 10.1021/ja010462s10.1021/ja010462s ↗
22. 10.1039/b201013p10.1039/b201013p ↗
23. 10.1021/ja016954m10.1021/ja016954m ↗
24. 10.1021/ja026086910.1021/ja0260869 ↗
25. 10.1021/ja029931w10.1021/ja029931w ↗
26. 10.1002/anie.20046121710.1002/anie.200461217 ↗
27. 10.1002/1521-3773(20020715)41:14<2508::AID-ANIE2508>3.0.CO;2-A10.1002/1521-3773(20020715)41:14<2508::AID-ANIE2508>3.0.CO;2-A ↗
28. 10.1021/ja029233b10.1021/ja029233b ↗
29. 10.1021/ja034082d10.1021/ja034082d ↗
30. 10.1021/ja037142o10.1021/ja037142o ↗
31. 10.1021/ja049202b10.1021/ja049202b ↗
32. T. S. Balaban A. T. Balaban inScience of Synthesis—Houben–Weyl Methods of Molecular Transformations(Ed: J. Thomas) Thieme Stuttgart Germany2003 Vol. 14 Ch. 14.1 pp. 11–200.
33. 10.1039/B401401D10.1039/B401401D ↗
34. 10.1021/ja00184a05310.1021/ja00184a053 ↗
35. 10.1126/science.108653410.1126/science.1086534 ↗
36. 10.1021/ol050862a10.1021/ol050862a ↗
37. 10.1021/ja052870s10.1021/ja052870s ↗
38. 10.1039/b204366a10.1039/b204366a ↗
39. 10.1002/adem.20050010610.1002/adem.200500106 ↗
40. E. Clar The Aromatic Sextet Wiley London UK1972.
41. 10.1080/1040663049042412410.1080/10406630490424124 ↗
42. 10.1021/ci050196s10.1021/ci050196s ↗
43. 10.1039/b201570f10.1039/b201570f ↗
44. 10.1039/b208270e10.1039/b208270e ↗