Interactions of Phenyldithioesters with Gold Nanoparticles (AuNPs): Implications for AuNP Functionalization and Molecular Barcoding of AuNP Assemblies

被引:33
作者
Blakey, Idriss [1 ,2 ]
Schiller, Tara L. [3 ]
Merican, Zul [1 ,2 ]
Fredericks, Peter M. [3 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Ctr Magnet Resonance, Brisbane, Qld 4072, Australia
[3] Queensland Univ Technol, Sch Phys & Chem Sci, Brisbane, Qld 4001, Australia
基金
澳大利亚研究理事会;
关键词
ENHANCED RAMAN-SCATTERING; DEPOLARIZED LIGHT-SCATTERING; RAFT POLYMERIZATION; CHARGE-TRANSFER; METAL; SILVER; SERS; SPECTROSCOPY; POLYMERS; SPECTRA;
D O I
10.1021/la9023162
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interactions of phenyldithioesters with gold nanoparticles (AuNPs) have been studied by monitoring changes in the surface plasmon resonance (SPR), depolarised light scattering, and surface enhanced Raman spectroscopy (SERS). Changes in the SPR indicated that an AuNP-phenyldithioester charge transfer complex forms in equilibrium with free AuNPs and phenyldithioester. Analysis of the Langmuir binding isotherms indicated that the equilibrium adsorption constant, K-ads, was 2.3 +/- 0.1 x 10(6) M-1, which corresponded to it free energy of adsorption of 36 +/- 1 kJ mol(-1). These values are comparable to those reported for interactions of aryl thiols with gold and are of a similar order of magnitude to moderate hydrogen bonding interactions. This has significant implications in the application of phenyldithioesters for the functionalization of AuNPs. The SERS results indicated that the phenyldithioesters interact with AuNPs through the C=S bond, and the molecules do not disassociate upon adsorption to the AuNPs. The SERS spectra are dominated by the portions of the molecule that dominate the charge transfer complex with the AuNPs. The significance of this in relation to the use of phenyldithioesters for molecular barcoding of nanoparticle assemblies is discussed.
引用
收藏
页码:692 / 701
页数:10
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