Synthesis, characterisation and electrical properties of supramolecular DNA-templated polymer nanowires of 2,5-(bis-2-thienyl)-pyrrole

Chemistry - A European Journal

Volumn 18, Issue 38, 2012, Pages 12008-12019

  Watson, Scott M D ^a   Hedley, Joseph H ^a   Galindo, Miguel A ^a   Al Said, Said A F ^a   Wright, Nick G ^a   Connolly, Bernard A ^a   Horrocks, Benjamin R ^a   Houlton, Andrew ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

conducting materials; DNA; nanowires; supramolecular polymers; templating

Indexed keywords

AFM; AQUEOUS/ORGANIC SOLVENTS; ARRHENIUS; BULK MATERIALS; CONDUCTING MATERIALS; CONDUCTIVE AFM; FTIR; HOPPING MODELS; I-V MEASUREMENTS; IN-BAND; MOLECULAR DYNAMICS SIMULATIONS; NON-COPLANAR CONFORMATIONS; NUCLEOBASES; PHOSPHODIESTERS; POLYMER NANOWIRES; REDOX POLYMERS; RESULTING MATERIALS; SPECTROSCOPIC STUDIES; SUPRAMOLECULAR POLYMERS; TEMPERATURE DEPENDENCE; TEMPLATING; VARIABLE TEMPERATURE;

AROMATIC COMPOUNDS; DNA; HYDROGEN BONDS; MOLECULAR DYNAMICS; NANOWIRES; POLYMERS; POLYPYRROLES; SPECTROSCOPIC ANALYSIS; SUPRAMOLECULAR CHEMISTRY;

ELECTRIC PROPERTIES;

2,5 (BIS 2 THIENYL) PYRROLE; 2,5-(BIS-2-THIENYL)-PYRROLE; CHLORIDE; DNA; FERRIC CHLORIDE; FERRIC ION; NANOWIRE; POLYMER; PYRROLE DERIVATIVE;

ARTICLE; CHEMISTRY; CONFORMATION; ELECTRIC CONDUCTIVITY; INFRARED SPECTROSCOPY; OXIDATION REDUCTION REACTION; SYNTHESIS; TEMPERATURE;

CHLORIDES; DNA; ELECTRIC CONDUCTIVITY; FERRIC COMPOUNDS; MOLECULAR CONFORMATION; NANOWIRES; OXIDATION-REDUCTION; POLYMERS; PYRROLES; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; TEMPERATURE;

EID: 84866241611     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201201495     Document Type: Article

References (74)

1. A. J. Heeger, Angew. Chem. 2001, 113, 2660-2682
2. Angew. Chem. Int. Ed. 2001, 40, 2591-2611.
3. T. A. Skotheim, R. L. Elsenbaumer, J. R. Reynolds, Handbook of Conducting Polymers, 2 nd ed., Marcel Dekker, New York, 1998.
4. A. G. MacDiarmid, Angew. Chem. 2001, 113, 2649-2659
5. Angew. Chem. Int. Ed. 2001, 40, 2581-2590.
6. A. B. Kaiser, Rep. Prog. Phys. 2001, 64, 1-49.
7. C. Li, H. Bai, G. Shi, Chem. Soc. Rev. 2009, 38, 2397-2409.
8. H. Xin, F. S. Kim, S. A. Jenekhe, J. Am. Chem. Soc. 2008, 130, 5424-5425.
9. T. Salim, S. Sun, L. H. Wong, L. Xi, Y. L. Foo, Y. M. Lam, J. Phys. Chem. C 2010, 114, 9459-9468.
10. Y. Liang, L. Yu, Acc. Chem. Res. 2010, 43, 1227-1236.
11. F. Cheng, W. Tang, C. Li, J. Chen, H. Liu, P. Shen, S. Dou, Chem. Eur. J. 2006, 12, 3082-3088.
12. A. L. Dyer, C. R. G. Grenier, J. R. Reynolds, Adv. Funct. Mater. 2007, 17, 1480-1486.
13. Z. Bao, J. A. Rogers, H. E. Katz, J. Mater. Chem. 1999, 9, 1895-1904.
14. T. K. Tam, M. Pita, M. Motornov, I. Tokarev, S. Minko, E. Katz, Adv. Mater. 2010, 22, 1863-1866.
15. K. Wang, J. Huang, Z. Wei, J. Phys. Chem. C 2010, 114, 8062-8067.
16. F. Wang, H. Gu, T. M. Swager, J. Am. Chem. Soc. 2008, 130, 5392-5393.
17. C. M. Hangarter, M. Bangar, A. Mulchandani, N. V. Myung, J. Mater. Chem. 2010, 20, 3131-3140.
18. Y. Xia, P. Yang, Y. Sun, Y. Wu, B. Mayers, B. Gates, Y. Yin, F. Kim, H. Yan, Adv. Mater. 2003, 15, 353-389.
19. S. Pruneanu, S. A. F. Al-Said, L. Dong, T. A. Hollis, M. A. Galindo, N. G. Wright, A. Houlton, B. R. Horrocks, Adv. Funct. Mater. 2008, 18, 2444-2454.
20. H. D. Tran, D. Li, R. B. Kaner, Adv. Mater. 2009, 21, 1487-1499.
21. M. Hasegawa, M. Iyoda, Chem. Soc. Rev. 2010, 39, 2420-2427.
22. A. Houlton, S. M. D. Watson, Annu. Rep. Prog. Chem. A 2011, 107, 21-42.
23. Y. Berdichevsky, Y.-H. Lo, Adv. Mater. 2006, 18, 122-125.
24. M. G. Han, S. H. Foulger, Chem. Commun. 2005, 3092-3094.
25. A. Drury, S. Chaure, M. Kröll, V. Nicolosi, N. Chaure, W. J. Blau, Chem. Mater. 2007, 19, 4252-4258.
26. C.-G. Wu, T. Bein, Science 1994, 264, 1757-1759.
27. C.-G. Wu, T. Bein, Chem. Mater. 1994, 6, 1109-1112.
28. J. Jang, B. Lim, J. Lee, T. Hyeon, Chem. Commun. 2001, 83-84.
29. J. Jang, H. Yoon, Chem. Commun. 2003, 720-721.
30. X. Zhang, J. Zhang, Z. Liu, C. Robinson, Chem. Commun. 2004, 1852-1853.
31. J. Jang, H. Yoon, Langmuir 2005, 21, 11484-11489.
32. X. Zhang, J. Zhang, W. Song, Z. Liu, J. Phys. Chem. B 2006, 110, 1158-1165.
33. Y. Ma, J. Zhang, G. Zhang, H. He, J. Am. Chem. Soc. 2004, 126, 7097-7101.
34. P. Nickels, W. U. Dittmer, S. Beyer, J. P. Kotthaus, F. C. Simmel, Nanotechnology 2004, 15, 1524.
35. L. Dong, T. Hollis, S. Fishwick, B. A. Connolly, N. G. Wright, B. R. Horrocks, A. Houlton, Chem. Eur. J. 2007, 13, 822-828.
36. S. A. Farhaa Al-Said, R. Hassanien, J. Hannant, M. A. Galindo, S. Pruneanu, A. R. Pike, A. Houlton, B. R. Horrocks, Electrochem. Commun. 2009, 11, 550-553.
37. J. Hannant, J. H. Hedley, J. Pate, A. Walli, S. A. Farhaa Al-Said, M. A. Galindo, B. A. Connolly, B. R. Horrocks, A. Houlton, A. R. Pike, Chem. Commun. 2010, 46, 5870-5872.
38. R. Hassanien, M. Al-Hinai, S. A. Farhaa Al-Said, R. Little, L. Siller, N. G. Wright, A. Houlton, B. R. Horrocks, ACS Nano 2010, 4, 2149-2159.
39. E. Buhler, S. J. Candau, E. Kolomiets, J. M. Lehn, Phys. Rev. E 2007, 76, 061804.
40. A. Ciesielski, G. Schaeffer, A. Petitjean, J. M. Lehn, P. Samori, Angew. Chem. 2009, 121, 2073-2077
41. Angew. Chem. Int. Ed. 2009, 48, 2039-2043.
42. M. Ikeda, T. Nobori, M. Schmutz, J. M. Lehn, Chem. Eur. J. 2005, 11, 662-668.
43. N. Sreenivasachary, D. T. Hickman, D. Sarazin, J. M. Lehn, Chem. Eur. J. 2006, 12, 8581-8588.
44. M. Kofranek, T. KováÅ, A. Karpfen, H. Lischka, J. Phys. Chem. 1992, 96, 4464
45. R. Kostić, D. Raković, S. A. Stepanyan, I. E. Davidova, L. A. Gribov, J. Chem. Phys. 1995, 102, 3104.
46. G. I. Dovbeshko, N. Y. Gridina, E. B. Kruglova, O. P. Pashchuk, Talanta 2000, 53, 233-246.
47. V. Andrushchenko, J. H. Vana dea Sande, H. Wieser, Biopolymers 2003, 72, 374-390.
48. A. A. Ouameur, H.-A. Tajmir-Riahi, J. Biol. Chem. 2004, 279, 42041-42054
49. H. Arakawa, R. Ahmad, M. Naoui, H. Tajmir-Riahi, J. Biol. Chem. 2000, 275, 10150.
50. C. Briones, E. Mateo-Marti, C. Gõmez-Navarro, V. Parro, E. Román, J. A. Martín-Gago, Phys. Rev. Lett. 2004, 93, 208103.
51. C.-Y. Lee, P. Gong, G. M. Harbers, D. W. Grainger, D. G. Castner, L. J. Gamble, Anal. Chem. 2006, 78, 3316-3325.
52. M. R. Vilar, A. M. Botelhoa doa Rego, A. M. Ferraria, Y. Jugnet, C. Noguès, D. Peled, R. Naaman, J. Phys. Chem. B 2008, 112, 6957-6964.
53. P. Pfluger, G. B. Street, J. Chem. Phys. 1984, 80, 544-553.
54. L. Atanasoska, K. Naoi, W. H. Smyrl, Chem. Mater. 1992, 4, 988-994.
55. J. Joo, J. K. Lee, S. Y. Lee, K. S. Jang, E. J. Oh, A. J. Epstein, Macromolecules 2000, 33, 5131-5136.
56. F. Buckel, F. Effenberger, C. Yan, A. Gölzhäuser, M. Grunze, Adv. Mater. 2000, 12, 901-905.
57. J. Li, C. Bai, C. Wang, C. Zhu, Z. Lin, Q. Li, E. Cao, Nucleic Acids Res. 1998, 26, 4785-4786.
58. Z. Deng, C. Mao, Nano Lett. 2003, 3, 1545-1548.
59. E. Braun, Y. Eichen, U. Sivan, G. Ben-Yoseph, Nature 1998, 391, 775-778.
60. J. Richter, M. Mertig, W. Pompe, I. Monch, H. K. Schackert, Appl. Phys. Lett. 2001, 78, 536-538.
61. M. Bockrath, N. Markovic, A. Shepard, M. Tinkham, L. Gurevich, L. P. Kouwenhoven, M. W. Wu, L. L. Sohn, Nano Lett. 2002, 2, 187-190.
62. C. Staii, A. T. Johnson, N. J. Pinto, Nano Lett. 2004, 4, 859-862.
63. T. S. Jespersen, J. Nygard, Nano Lett. 2005, 5, 1838-1841.
64. A. L. Efros, B. I. Shklovskii, J. Phys. Chem. C 1975, 8, L49-L51.
65. S. Chakrabarti, D. Banerjee, R. Bhattacharyya, J. Phys. Chem. B 2002, 106, 3061-3064.
66. C. C. Bofa Bufon, T. Heinzel, Phys. Rev. B 2007, 76, 245206.
67. J.-M. Saveant, J. Electroanal. Interfac. Chem. 1986, 201, 211-213
68. C. P. Andrieux, J.-M. Saveant, J. Phys. Chem. B 1988, 92, 6761-6767.
69. J. C. Jernigan, R. W. Murray, J. Phys. Chem. 1987, 91, 2030-2032.
70. R. H. Terrill, J. E. Hutchison, R. W. Murray, J. Phys. Chem. B 1997, 101, 1535-1542.
71. E. F. Dalton, N. A. Surridge, J. C. Jernigan, K. O. Wilbourn, J. S. Facci, R. W. Murray, Chem. Phys. 1990, 141, 143-157.
72. R. E. Niziurski-Mann, M. P. Cava, Adv. Mater. 1993, 5, 547-551.
73. Wavefunction, Inc., Irvine, CA, 2004.
74. Accelrys, Inc., San Diego, CA 92121, USA.