journal article·2008-05-01

Light-Induced Aggregation of Colloidal Gold Nanoparticles Capped by Thymine Derivatives

Jingfang Zhou, Rossen Sedev, David Beattie, John Ralston

Langmuir· Volume 24· Issue 9
Publisher page

Abstract

The colloid stability of thymine-coated gold nanoparticles under light irradiation as a function of particle size, surface charge, and exposure time was investigated in alkaline, aqueous solutions as well as in a 0.5 vol % of DMF in H(2)O mixture. With increasing exposure to light irradiation at 280 nm, more and more particles coagulated. Light-induced aggregation of colloidal gold nanoparticles was attributed to reorientation of thymine terminal groups tethered on gold particle surfaces. A smaller particle size and negatively charged surface reduced the rate of photodimerization or even inhibited the photoreaction. UV-vis and FTIR spectroscopy confirmed the photodimerization of terminal thymine molecules under 280 nm light irradiation. The reaction kinetics of thymine photodimerization appears to be a combination of first-order reactions, each having different rates, reflecting the inhomogeneity and high curvature of the gold nanoparticle surfaces.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanocluster Synthesis and Applications · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Ian Wark Research Institute, University of South Australia, Mawson Lakes, Adelaide, South Australia 5095

References (58)

Show source-provided references
1. Watanabe K. · Chem. Rev. · 2006 · 106 · 432010.1021/cr050167g ↗
2. Daniel M. C. · Chem. Rev. · 2004 · 104 · 34610.1021/cr030698+ ↗
3. Bonnemann H. · Eur. J. Inorg. Chem. · 2001 · 2455 · 2480
4. Hiemenz P. C. · 1997
5. Lyklema J. H. · 2005 · 4
6. Suzuki D. · J. Phys. Chem. C · 2007 · 111 · 5672
7. Ballauff M. · Polymer · 2007 · 48 · 182310.1016/j.polymer.2007.02.004 ↗
8. Li D. · Chem.Eur. J. · 2007 · 13 · 2229
9. Zhang J. · Langmuir · 2007 · 23 · 6351
10. Racuciu M. · J. Optoelectron. Adv. Mater. · 2007 · 9 · 1533
11. Evans S. D. · Langmuir · 1998 · 14 · 644010.1021/la980450t ↗
12. Bell N. S. · Langmuir · 2006 · 22 · 1427
13. Ueda M. · J. Mater. Chem. · 1997 · 7 · 64510.1039/a607145g ↗
14. Ueda M. · J. Mater. Chem. · 1994 · 4 · 88910.1039/jm9940400883 ↗
15. Zhang J. · Chem. Mater. · 2001 · 13 · 2331
16. Hu J. · J. Am. Chem. Soc · 2001 · 123 · 1470
17. Ipe B. I. · J. Am. Chem. Soc · 2003 · 125 · 7175
18. Manna A. · Chem. Mater. · 2003 · 15 · 2810.1021/cm0207696 ↗
19. Sidhaye D. S. · Langmuir · 2005 · 21 · 798410.1021/la051125q ↗
20. Inaki Y. · Senryo to Yakuhin · 1991 · 36 · 55
21. Lamola A. · Science · 1966 · 154 · 156110.1126/science.154.3756.1560 ↗
22. Greenstock C. L. · Biochem. Biophys. Res. Commun · 1967 · 27 · 43610.1016/S0006-291X(67)80002-0 ↗
23. Inaki Y. · 1993
24. Tohnai N. · J. Photopolym. Sci. Technol. · 1994 · 7 · 210.2494/photopolymer.7.91 ↗
25. Li C. · Langmuir · 2001 · 17 · 2234
26. Kita Y. · 1980
27. Kita Y. · 1981
28. Inaki Y. · J. Photopolym. Sci. Technol. · 2000 · 13 · 182
29. Mochizuki E. · Bull. Chem. Soc. Jpn. · 2001 · 74 · 20010.1246/bcsj.74.193 ↗
30. Itoh H. · Langmuir · 2004 · 20 · 197610.1021/la0359777 ↗
31. Lake N. · Lamgmuir · 2005 · 21 · 1193110.1021/la051457v ↗
32. Abbott S. · Langmuir · 1999 · 15 · 892810.1021/la990558o ↗
33. Zhou J. · Langmuir · 2007 · 23 · 9177
34. Zhou J. · Langmuir · 2007 · 12096 · 12103
35. Rouhana L. L. · Langmuir · 2007 · 23 · 1280110.1021/la702151q ↗
36. Fornasiero D. · J. Colloid Interface Sci. · 1991 · 141 · 17910.1016/0021-9797(91)90312-V ↗
37. Karpov S. V. · Colloid J. · 2002 · 64 · 44110.1023/A:1016811818799 ↗
38. Beukers R. · Biochim. Biophys. Acta · 1960 · 41 · 55110.1016/0006-3002(60)90063-9 ↗
39. Herbert M. A. · Photochem. Photobiol. · 1969 · 9 · 4310.1111/j.1751-1097.1969.tb05907.x ↗
40. Wulff D. L. · Biochim. Biophys. Acta · 1961 · 51 · 33910.1016/0006-3002(61)90174-3 ↗
41. Briggs, D.; Riviere, J. C.Spectral Interpretation; Wiley: Chichester, 1990.
42. Rastogi V. K. · J. Raman Spectrosc. · 2000 · 31 · 1012
43. Silverstein R. M. · 1998
44. Bergmann F. · J. Am. Chem. Soc. · 1955 · 77 · 696
45. Shim S. C. · Photochem. Photobiol. · 1979 · 29 · 1038
46. Mochizuki E. · Kobunshi Kako · 1999 · 48 · 497
47. Wagner P. J. · J. Am. Chem. Soc · 1970 · 92 · 185
48. 1991
49. Inaki Y. · J. Photopolym. Sci. Tech. · 2000 · 13 · 182
50. Inaki, Y.CRC Handbook of Organic Photochemistry andPhotobiology,2nd ed; Boca Raton, FL, 2004; pp 104/1−104/34.
51. Tohnai N. · Bull. Chem. Soc. Jpn. · 1999 · 72 · 858
52. Tohnai N. · Bull. Chem. Soc. Jpn. · 1999 · 72 · 1151
53. Templeton A. C. · J. Am. Chem. Soc. · 1998 · 120 · 1911
54. Hostetler M. J. · Langmuir · 1998 · 14 · 3010.1021/la970588w ↗
55. Mochizuki E. · Polym. J. (Tokyo) · 2000 · 32 · 50010.1295/polymj.32.492 ↗
56. Tohnai N. · J. Photopolym. Sci. Technol. · 1994 · 7 · 9210.2494/photopolymer.7.91 ↗
57. Thomas K. G. · Pure Appl. Chem. · 2002 · 74 · 173810.1351/pac200274091731 ↗
58. Zhang J. · J. Phys. Chem. B · 2003 · 107 · 605510.1021/jp034592u ↗