Proton nuclear magnetic resonance (NMR) was used to measure the rate constant and activation energy barrier for electron self-exchanges of the phenylethanethiolate-protected nanoparticle couple [Au 25 (SC2Ph) 18 ] 0/1− . The thiolate ligand α-methylene proton resonances of electrolytically prepared CD 2 Cl 2 solutions of the oxidized (Au 25 0 ) and reduced (Au 25 1− ) nanoparticles exhibit characteristic chemical shifts and line-shapes. That for the α-CH 2 protons in Au 25 0 is shifted ∼2 ppm downfield from Au 25 1− and has an increased line-width reflecting the odd electron count of the nanoparticle core. Solution mixtures of Au 25 0 and Au 25 1− exhibit further peak broadening and intermediate values of α-CH 2 proton chemical shifts, effects quantitatively consistent with an electron self-exchange process in the fast-exchange regime. Analysis of changes in peak broadening at varied total nanoparticle concentration and at varied temperatures produces a rate constant for [Au 25 (SC2Ph) 18 ] 0/1− self-exchange of 3.0(±0.1) × 10 7 M −1 s −1 at 22 °C and an activation barrier energy E A = 25.0 (±1.5) kJ/mol. This barrier energy is much larger than the calculated estimate of outer-sphere reorganization energy, implying the presence of a significant inner-sphere reorganization energy. The latter is confirmed by a detected difference in the Raman Au−S bond stretch energies of Au 25 0 and Au 25 1− nanoparticles.
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Parker et al. (2008) studied this question.
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