Controlled plasmon resonance of gold nanoparticles self-assembled with PAMAM dendrimers

Chemistry of Materials

Volumn 17, Issue 3, 2005, Pages 487-490

  Srivastava, Sudhanshu ^a   Frankamp, Benjamin L ^a   Rotello, Vincent M ^a  

^a UNIVERSITY OF MASSACHUSETTS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; DENDRIMERS; GOLD; MODULATION; OPTICAL PROPERTIES; SCATTERING; SELF ASSEMBLY; X RAYS;

DENDRIMER ASSEMBLY; GOLD NANOPARTICLES; SMALL-ANGLE X-RAY SCATTERING (SAXS); STRUCTURAL CONTROL;

NANOSTRUCTURED MATERIALS;

CARBOXYLIC ACID; DENDRIMER; GOLD; METHANOL; POLY(AMIDOAMINE); POLYAMINE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; COMPOSITE MATERIAL; DIPOLE; NANOPARTICLE; OPTICAL ROTATION; SURFACE PLASMON RESONANCE; SYNTHESIS; TRANSMISSION ELECTRON MICROSCOPY; ULTRAVIOLET SPECTROSCOPY; X RAY CRYSTALLOGRAPHY;

EID: 13444252774     PISSN: 08974756     EISSN: None     Source Type: Journal    
DOI: 10.1021/cm048579d     Document Type: Article

References (32)

1. Wessels, J. M.; Nothofer, H. G.; Ford, W. E.; von Wrochem, F.; Scholz, F.; Vossmeyer, T.; Schroedter, A.; Weller, H.; Yasuda, A. J. Am. Chem. Soc. 2004, 126, 3349-3356.
2. Sun, Y. G.; Xia, Y. N. Anal. Chem. 2002, 74, 5297-5305.
3. (a) Sershen, S. R.; Westcott, S. L.; West, J. L.; Halas, N. J. Appl. Phys. B-Lasers Opt. 2001, 73, 379.
4. (b) Tominaga, J. J. Phys.-Condes. Matter 2003, 15, R1101-R1122.
5. (a) Kreilbig, U.; Vollmer, M. Optical Properties of Metal Clusters; Springer-Verlag: Berlin, 1996.
6. (b) Wei, A. Nanoparticles Building blocks for Nanotechnology; Rotello, V. M.; Kluwer Academic/Plenium Publishers: New York, 2004; pp 173-200.
7. (a) Homola, J. Anal. Bioanal. Chem. 2003, 377, 528-539.
8. (b) Saponjic, Z. V.; Csencsits, R.; Rajh, T.; Dimitrijevic, N. M. Chem. Mater. 2003, 15, 4521-4526.
9. McConnell, W. P.; Novak, J. P.; Brousseau, L. C.; Fuierer, R. R.; Tenent, R. C.; Feldheim, D. L. J. Phys. Chem. B 2000, 104, 8925-8930.
10. Rechberger, W.; Hohenau, A.; Leitner, A.; Krenn, J. R.; Lamprecht, B.; Aussenegg, F. R. Opt. Commun. 2003, 220, 137-141.
11. (a) Schmitt, J.; Decher, G.; Dressick, W. J.; Brandow, S. L.; Geer, R. E.; Shashidhaar, R.; Calvert, J. M. Adv. Mater. 1997, 9, 61-65.
12. (b) Malikova, N.; Pastoriza-Santos, I.; Schierhorn, M.; Kotov, N. A.; Liz-Marzan, L. M. Langmuir 2002, 18, 3694-3697.
13. (a) Liz-Marzan, L. M.; Mulvaney, P. J. Phys. Chem. B 2003, 107, 7312-7326.
14. (b) Collier, C. P.; Saykally, R. J.; Shiang, J. J.; Henrichs, S. E.; Heath, J. R. Science 1997, 277, 1978-1981.
15. Liz-Marzan, L. M.; Giersig, M.; Mulvaney, P. Langmuir 1996, 12, 4329-4335.
16. Ung, T.; Liz-Marzan, L. M.; Mulvaney, P. J. Phys. Chem. B 2001, 105, 3441-3452.
17. For other results based on interparticle spacing see: (1) Schmitt, J.; Mächtle, P.; Eck, D.; Möhwald, H.; Helm, C. A. Langmuir 1999, 15, 3256-3266.
18. Hövel, H.; Fritz, S.; Hilger, A.; Kreibig, U. Phys. Rev. B 1993, 48, 18178-18188.
19. Among the various effective medium theories available, it has been found that the Maxwell-Garnett theory is suitable to describe these dipole-dipole interactions; see: Maxwell-Garnett, J. C. Philos. Trans. R. Soc. London; 1904, 203, p 385.
20. (a) West, J. L.; Halas, N. J. Annu. Rev. Biomed. Eng. 2003, 5, 285-292.
21. (b) Storhoff, J. J.; Lazarides, A. A.; Mucic, R. C.; Mirkin, C. A.; Letsinger, R. L.; Schatz, G. C. J. Am. Chem. Soc. 2000, 122, 4640-4650.
22. Frankamp, B. L.; Boal, A. K.; Rotello, V. M. J. Am. Chem. Soc. 2002, 124, 15146-15147.
23. Teranishi, T.; Hasegawa, S.; Shimizu, T.; Miyake, M. Adv. Mater. 2001, 13, 1699-1701.
24. Carroll, J. B.; Frankamp, B. L.; Srivastava, S.; Rotello, V. M. J. Mater. Chem. 2004, 14, 690-694.
25. (a) He, J. A.; Valluzzi, R.; Yang, K.; Dolukhanyan, T.; Sung, C. M.; Kumar, J.; Tripathy, S. K.; Samuelson, L.; Balogh, L.; Tomalia, D. A. Chem. Mater. 1999, 11, 3268-3274,
26. (b) Sooklal, K.; Hanus, L. H.; Ploehn, H. J.; Murphy, C. J. Adv. Mater. 1998, 10, 1083-1087.
27. Dendritech web site: Dendritech.com.
28. Lazarides, A. A.; Schatz, G. C. J. Chem. Phys. 2000, 112, 2987-2993.
29. To ensure sample consistency, the exact same MMPC 1/PAMAM samples were used for SAXS and UV analysis.
30. Kinetic experiments were carried out at room temperature with slightly lower overall concentration, to allow for optical transparency, while the relative ratio of MMPC 1 and PAMAM dendrimer remained constant.
31. PAMAM generation 6 never precipitated, even though the molar ratios of nanoparticle to dendrimer are identical in all cases.
32. Boal, A. K.; Galow, T. H.; Ilhan, F.; Rotello, V. M. Adv. Fund. Mater. 2001, 11, 461-465.