Monolayers in three dimensions: NMR, SAXS, thermal, and electron hopping studies of alkanethiol stabilized gold clusters

Gold clusters stabilized by chemisorbed monolayers of octane-, dodecane- or hexadecanethiolate have been investigated in solution and in the solid phase. These materials can be pumped free of solvent to form a dark brown solid that can be re-dissolved in nonpolar solvents. Their exceptional stability suggests they be viewed as cluster compounds. The self-assembled alkanethiolate monolayers stabilizing the metal clusters can be investigated using techniques that are insufficiently sensitive for study of a monolayer on a flat surface, e.g., H-1 and C-13 NMR, elemental analysis, differential scanning calorimetry (DSC), thermogravimetry (TGA), and diffusion-ordered NMR spectroscopy (DOSY). Results from such measurements, combined with small-angle X-ray scattering (SAXS) data on solutions of the clusters and images from scanning tunneling (STM), and atomic force microscopy (AFM), are consistent with a small, monodisperse (12 Angstrom radius) gold core, which modeled as a sphere contains similar to 400 Au atoms and similar to 126 alkanethiolate chains, or if modeled as a cuboctahedral structure contains 309 Au atoms and similar to 95 alkanethiolate chains. High-resolution NMR spectra of cluster solutions display well-defined resonances except for methylenes nearest the gold interface; the absence of the latter resonances is attributed to a combination of broadening mechanisms based on the discontinuous change in magnetic susceptibility at the metal-hydrocarbon interface and residual dipolar interactions. Films of the dry, solid cluster compound on interdigitated array electrodes exhibit current-potential responses characteristic of electron hopping conductivity in which electrons tunnel from Au core to Au core. The electron hopping rate decreases and the activation barrier increases systematically at longer alkane chain length. The results are consistent with electron transport rate control being a combination of thermally activated electron transfer to create oppositely charged Au cores (cermet theory) and distance-dependent tunneling (beta = 1.2 Angstrom(-1)) through the oriented alkanethiolate layers separating them.