Mass Spectrometry of Ligand Exchange Chelation of the Nanoparticle [Au25(SCH2CH2C6H5)18]1- by CH3C6H3(SH)2

被引:40
作者
Fields-Zinna, Christina A. [1 ]
Parker, Joseph F. [1 ]
Murray, Royce W. [1 ]
机构
[1] Univ N Carolina, Kenan Labs Chem, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
SELF-ASSEMBLED MONOLAYERS; GOLD NANOPARTICLES; CLUSTER; THIOLATE; FUNCTIONALIZATION; ADSORPTION; COMPLEXES; AU(111); DRUGS; AU-25;
D O I
10.1021/ja106243g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mass spectrally detected products of ligand exchange reactions of the nanoparticle [Au-25(SC2H4C6F15)(18)](1-), (abbrev. Au-25(SC2Ph)(18)), where the dithiol is toluene-3,4-dithiol, CH3C6F13(SH)(2), include nanoparticles containing both doubly (bidentate, or chelating) and singly bonded dithiol. The bidentate binding displaces two of the original -SC2Ph ligands, and singly bonded dithiol displaces one -SC2Ph ligand, while maintaining, for mass spectrally detected species, occupancy of 18 ligation sites. Extended exchange reaction times result in an apparent maximum of six chelated dithiolates. In the Au-25(SC2Ph)(18) naroparticle, six semi-rings of -S(R)-Au-S(R)-Au-S(R)- act as the protecting ligand shell surrounding a Au-13 core; the chelation is suggested to involve binding of dithiolates to adjacent semi-rings, rather than to a single semi-ring. Both high resolution ESI and lower resolution MALDI spectra support the product assignments. A minor extent of bidentate ligand incorporation is sufficient to severely compromise the well-known Au-25(SC2Ph)(18) UV-vis fine structure and to alter its voltammetric pattern, reflecting either associated semi-ring distortion and/or decay of the exchange product.
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页码:17193 / 17198
页数:6
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