Reverse micellar synthesis of dye/gold hybrid nanocomposites

Chemistry Letters

Volumn 39, Issue 5, 2010, Pages 504-505

  Takahashi, Masaki ^a   Ohno, Shuhei ^a   Fujita, Norifumi ^b   Sengoku, Tetsuya ^a   Yoda, Hidemi ^a,c  

^a SHIZUOKA UNIVERSITY   (Japan)

^b KYUSHU UNIVERSITY   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 77951542185     PISSN: 03667022     EISSN: 13480715     Source Type: Journal    
DOI: 10.1246/cl.2010.504     Document Type: Article

References (33)

1. P. N. Prasad, Nanophotonics, John Wiley &. Sons, inc., Hoboken, NJ, 2004, Chap. 5, pp. 129-151.
2. M.-C. Daniel, D. Astruc, Chem. Rev. 2004, 104, 293.
3. a) Y. Negishi, T. Tsukuda, J. Am. Chem. Soc, 2003, 125, 4046.
4. b) H. Tsunoyama, T. Tsukuda, J. Am. Chem. Soc, 2009, 131, 18216.
5. M. Schulz-Dobrick, K. V. Sarathy, M. Jansen, J. Am. Chem. Soc. 2005, 127, 12816.
6. a)S. Lee, E.-J. Cha, K. Park, S.-Y. Lee, J.-K. Hong, I.-C. Sun, S. Y. Kim, K. Choi, I. C. Kwon, K. Kim, C.-H. Ahn, Angew. Chem., Int. Ed. 2008, 47, 2804.
7. b) T. Selvaraju, J. Das, K. Jo, K. Kwon, C.-H. Huh, T. K. Kim, H. Yang, Langmuir 2008, 24, 9883.
8. J. Homola, Chem. Rev. 2008, 108, 462.
9. a) J. Kim, S. Park, J. E. Lee, S. M. Jin, J. H. Lee, I. S. Lee, I. Yang, J.-S. Kim, S. K. Kim, M.-H. Cho, T. Hyeon, Angew. Chem., Int. Ed. 2006, 45, 7754.
10. b) Y.-F. Huang, K. Sefah, S. Bamrangsap, H.-T. Chang, W. Tan, Langmuir 2008, 24, 11860.
11. S. Lal, S. E. Clare, N. J. Halas, Acc. Chem. Res. 2008, 41, 1842.
12. a) R. I. Nooney, O. Stranik, C. McDonagh, B. D. MacCraith, Langmuir 2008, 24, 11261
13. b) P. Zijlstra, J. W. M. Chon, M. Gu, Nature 2009, 459, 410.
14. D. V. Talapin, J.-S. Lee, M. V. Kovalenko, E. V. Shevchenko, Chem. Rev. 2010, 110, 389.
15. a) K. G. Thomas, P. V. Kamat, Acc. Chem. Res. 2003, 36, 888.
16. b) W. J. M. Mulder, G. J. Strijkers, G. A. F. van Tilborg, D. P. Cormode, Z. A. Fayad, K. Nicolay, Acc. Chem. Res. 2009, 42, 904.
17. c) J. Gao, H. Gu, B. Xu, Acc. Chem. Res. 2009, 42, 1097.
18. M. Stemmler, F. D. Stefani, S. Bernhardt, R. E. Bauer, M. Kreiter, K. Müllen, W. Knoll, Langmuir 2009, 25, 12425.
19. B. J. Kim, G. H. Fredrickson, J. Bang, C. J. Hawker, E. J. Kramer, Macromolecules 2009, 42, 6193.
20. F. Cheng, K. Zhang, D. Chen, L. Zhu, M. Jiang, Macromolecules 2009, 42, 7108.
21. F. Gröhn, B. J. Bauer, Y. A. Akpalu, C. L. Jackson, E. J. Amis, Macromolecules 2000, 33, 6042.
22. T. Sakai, P. Alexandridis, Langmuir 2005, 21, 8019.
23. M. Zhu, E. Lanni, N. Garg, M. E. Bier, R. Jin, J. Am. Chem. Soc. 2008, 130, 1138.
24. M. Takahashi, Y. Ichihashi, N. Nishizawa, S. Ohno, N. Fujita, M. Yamashita, T. Sengoku, H. Yoda, J. Photochem. Photobiol., A 2009, 203, 56.
25. M. Takahashi, N. Nishizawa, S. Ohno, M. Kakita, N. Fujita, M. Yamashita, T. Sengoku, H. Yoda, Tetrahedron 2009, 65, 2669.
26. M. P. Pileni, Structure and Reactivity in Reverse Micelles, Elsevier, Amsterdam, Oxford, New York, Tokyo, 1989, pp. 198-220.
27. H. Fan, Chem. Commun. 2008, 1383.
28. Figures S1 and S2 are shown in Supporting Information. Supporting Information is available electronically on the CSJJoumal Web site, http://www.csj.jp/journals/chem.-lett/index. html.
29. As for electron-transfer fluorescence quenching of excited pyrene derivative by gold nanoparticle, see: P. V. Kamat, S. Barazzouk, S. Hotchandani, Angew. Chem., Int. Ed. 2002, 41, 2764.
30. As for similarity in free energy changes for electron-transfer fluorescence quenching of perylene and that of pyrene, see: T. N. Inada, K. Kikuchi, Y. Takahashi, H. Ikeda, T. Miyashi, J. Photochem. Photobiol, A 2000, 137, 93.
31. A solution of me dye/GNP aggregates diluted with dry toluene (c = 0.1 mM) was drop-cast on to the HOPG. Air-dried sample of this solution was examined by measurements in tapping mode.
32. Molecular modeling study of fully extended structure of 1 indicates that vertical distance from the perylene nucleus to the center of the molecular edges are estimated to be approximately 1.3 nm.
33. The observation that the sample incubated for 10 days revealed the SPR absorption band at the same wavelength suggested that nanostructures of the GNPs should be highly stabilized by the dye surfactants.