Synthesis and characterisation of controllably functionalised polyaniline nanofibres
Source abstract
Abstract
A novel method for functionalising solution based polyaniline (PAni) nanofibres is reported whereby the degree of side-chain attachment can be controllably altered. The covalent attachment of functional side-groups to the surface of PAni nanostructures is achieved by post-polymerisation reflux in the presence of a nucleophile and the functionalised nanomaterial can be purified by simple centrifugation. The technique is therefore easily scalable. We demonstrate that control over the extent of side-chain attachment can be achieved simply by altering the amount of nucleophile added during reflux. We provide evidence that covalently attached carboxylate side-chains influence the doping mechanism of polyaniline and can be used to introduce self-doping behaviour. Acid functionalised nanofibres remain redox active and retain their optical switching capabilities in response to changes in the local chemical environment, thus making them suitable for adaptive sensing applications.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Conducting polymers and applications · Electrochemical sensors and biosensors · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (45)
Show source-provided references
1. Drury · Chem. Mater. · 2007 · 19 · 425210.1021/cm071102s ↗
2. Belzig · Nat. Nanotechnol. · 2006 · 1 · 16710.1038/nnano.2006.161 ↗
3. Bao · Nano Lett. · 2006 · 6 · 171910.1021/nl061080t ↗
4. Nikoobakht · Chem. Mater. · 2007 · 19 · 527910.1021/cm071798p ↗
5. Ci · Adv. Mater. · 2007 · 19 · 330010.1002/adma.200602974 ↗
6. Blake · J. Am. Chem. Soc. · 2004 · 126 · 1022610.1021/ja0474805 ↗
7. Cui · Science · 2001 · 293 · 128910.1126/science.1062711 ↗
8. Jiang Yue · J. Am. Chem. Soc. · 1990 · 112 · 280010.1021/ja00163a051 ↗
9. Salavagione · Acta Polym. · 1999 · 50 · 4010.1002/(SICI)1521-4044(19990101)50:1<40::AID-APOL40>3.0.CO;2-8 ↗
10. Baker · Adv. Mater. · 2008 · 20 · 155−+10.1002/adma.200602864 ↗
11. Small · J. Mater. Chem. · 2007 · 17 · 435910.1039/b712940h ↗
12. Roh · J. Macromol. Sci.-Pure Appl. Chem. · 2002 · A39 · 109510.1081/MA-120014837 ↗
13. Byrne · Nat. Mater. · 2006 · 5 · 42110.1038/nmat1661 ↗
14. MacDiarmid · Synth. Met. · 1997 · 84 · 2710.1016/S0379-6779(97)80658-3 ↗
15. Chiou · Synth. Met. · 2005 · 153 · 6910.1016/j.synthmet.2005.07.145 ↗
16. Huang · Chem. Commun. · 2006 · 36710.1039/B510956F ↗
17. Li · Chem. Commun. · 2005 · 328610.1039/b504020e ↗
18. Li · J. Mater. Chem. · 2007 · 17 · 227910.1039/b700699c ↗
19. Chiou · Nat. Nanotechnol. · 2007 · 2 · 35410.1038/nnano.2007.147 ↗
20. Masdarolomoor · Macromol. Rapid Commun. · 2006 · 27 · 199510.1002/marc.200600598 ↗
21. Virji · Nano Lett. · 2004 · 4 · 49110.1021/nl035122e ↗
22. Virji · J. Phys. Chem. B · 2006 · 110 · 2226610.1021/jp063166g ↗
23. Virji · Chem. Mater. · 2005 · 17 · 125610.1021/cm0484091 ↗
24. Virji · Small · 2005 · 1 · 62410.1002/smll.200400155 ↗
25. Tseng · Nano Lett. · 2005 · 5 · 107710.1021/nl050587l ↗
26. Huang · J. Am. Chem. Soc. · 2003 · 125 · 31410.1021/ja028371y ↗
27. Tran · Chem. Commun. · 2006 · 391510.1039/b605928g ↗
28. Acevedo · J. Braz. Chem. Soc. · 2005 · 16 · 25910.1590/S0103-50532005000200020 ↗
29. Barbero · Synth. Met. · 1999 · 101 · 69410.1016/S0379-6779(98)00977-1 ↗
30. Acevedo · Faraday Discuss. · 2006 · 131 · 23510.1039/B505585G ↗
31. Han · Chem. Commun. · 1997 · 55310.1039/a608079k ↗
32. Lahiff · Carbon · 2006 · 44 · 152510.1016/j.carbon.2005.12.018 ↗
33. Goutev · Appl. Spectrosc. · 2003 · 57 · 50610.1366/000370203321666506 ↗
34. Castro · J. Raman Spectrosc. · 2004 · 35 · 99710.1002/jrs.1247 ↗
35. Hussain · Bull. Mater. Sci. · 2003 · 26 · 32910.1007/BF02707455 ↗
36. Moller · J. Mater. Chem. · 2007 · 17 · 62410.1039/B611931J ↗
37. Krishnakumar · Spectrochim. Acta Part a-Mol. Biomol. Spectrosc. · 2004 · 60 · 70910.1016/S1386-1425(03)00281-6 ↗
38. Luo · Polym. Degrad. Stab. · 2006 · 91 · 266010.1016/j.polymdegradstab.2006.04.027 ↗
39. Mazeikiene · Electrochem. Commun. · 2006 · 8 · 108210.1016/j.elecom.2006.04.017 ↗
40. Liu · J. Appl. Polym. Sci. · 2004 · 92 · 17110.1002/app.13706 ↗
41. Barbero · J. Mater. Chem. · 1994 · 4 · 177510.1039/JM9940401775 ↗
42. Yasuda · J. Mater. Chem. · 2003 · 13 · 213810.1039/b305760g ↗
43. Inoue · J. Mater. Chem. · 1994 · 4 · 181110.1039/jm9940401811 ↗
44. Xingwei Li · Mater. Lett. · 2008 · 62 · 143110.1016/j.matlet.2007.08.078 ↗
45. Masdarolomoor · Synth. Met. · 2005 · 153 · 18110.1016/j.synthmet.2005.07.249 ↗