Redox active gold nanoparticles modified with tetrathiafulvalene derivative via direct sulfur bridge

Inorganic Chemistry Communications

Volumn 8, Issue 11, 2005, Pages 994-997

  Guo, Wen Juan ^a   Dai, Jie ^a,b   Zhang, De Qing ^b   Zhu, Qin Yu ^a   Bian, Guo Qin ^a  

^a SOOCHOW UNIVERSITY   (China)

^b INSTITUTE OF CHEMISTRY   (China)

Author keywords

Cyclic voltammogram; Electrochemical response; Gold colloid; Gold nanoparticle; Tetrathiafulvalene

Indexed keywords

EID: 26844575213     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2005.08.001     Document Type: Article

References (25)

1. A.A. Lazarides, and G.C. Schatz J. Phys. Chem. B 104 2000 460
2. S.-J. Park, A.A. Lazarides, C.A. Mirkin, P.W. Brazis, C.R. Kannewurf, and R.L. Letsinger Angew. Chem. 39 2000 3845
3. L. Francois, M. Mostafavi, J. Belloni, J.-F. Delouis, J. Delaire, and P. Feneyrou J. Phys. Chem. B 104 2000 6133
4. P. Mulvaney Langmuir 12 1996 788
5. J. Wang, D. Xu, A.-N. Kawde, and R. Polsky Anal. Chem. 73 2001 5576
6. S.-F. Cheng, and L.-K. Chau Anal. Chem. 75 2003 16
7. D.J. Maxwell, J.R. Taylor, and S. Nie J. Am. Chem. Soc. 124 2002 9606
8. A. Schroedter, and H. Weller Angew. Chem. Int. Ed. 41 2002 3218
9. C.M. Niemeyer, and B. Ceyhan Angew. Chem. Int. Ed. 40 2001 3685
10. M.-C. Daniel, and D. Astruc Chem. Rev. 104 2004 293
11. A. Labande, J. Ruiz, and D. Astruc J. Am. Chem. Soc. 124 2002 1782
12. M.-C. Daniel, J. Ruiz, S. Nlate, J.-C. Blais, and D. Astruc J. Am. Chem. Soc. 125 2003 2617
13. M.-C. Daniel, J. Ruiz, J. Nlate, J. Palumbo, J.-C. Blais, and D. Astruc Chem. Commun. 2001 2000
14. A. Labande, J. Ruiz, and D. Astruc J. Am. Chem. Soc. 124 2002 1782
15. M.B. Nielsen, C. Lomholt, and J. Becher Chem. Soc. Rev. 29 2000 153
16. T. Jørgensen, T.K. Hansen, and J. Becher Chem. Soc. Rev. 1994 41
17. J.M. Williams, M.A. Beno, H.H. Wang, P.C.W. Leung, T.J. Emge, U. Geise, and K.D. Carlson Accounts Chem. Res. 18 1985 261
18. H. Najai, M. Yoshihara, and H. Fujihara Langmuir 15 1999 8574
19. J. Dai, L. Guo, Y. Jiang, Q.-Y. Zhu, R.-A. Gu, D.-X. Jia, and W.-J. Guo J. Nanosci. Nanotech. 5 2005 474
20. -1 for the C-H vibrations of the octyl groups. The elemental analysis result: Found: C, 52.20, H, 6.96, N, 2.37%; Calc: C, 51.98, H, 6.81, N, 2.43%.
21. C. Jia, D. Zhang, W. Xu, and D. Zhu Org. Lett. 3 2001 1941
22. K.R. Brown, D.G. Walter, and M.J. Natan Chem. Mater. 12 2000 306
23. 4NOH in MeOH to remove the 2-cyanoethyl group. The solution was added to the gold-colloid (20 ml) and the mixture was stirred for 30 min, resulting a clear dark-brown colloid. All the procedures were done under Ar atmosphere. After the modification finished the colloid was quite stable in ambient condition.
24. H. Liu, and J. Deng Electrochim. Acta 40 1995 1845
25. H. Liu, and J. Deng Anal. Chim. Acta 300 1995 65