The adsorption geometries of iodomethane, iodoethane, 1-iodopropane, and 2-iodopropane on Cu(110) single-crystal surfaces were characterized by using reflection−absorption infrared spectroscopy. At 100 K adsorption is molecular in all cases, but with adsorption geometries that change with increasing coverages. All alkyl iodides adsorb with the C−I bond perpendicular to the surface at low coverages and tilted at saturation. The hydrocarbon chains in iodoethane, 1-iodopropane, and 2-iodopropane follow the expected behavior, namely, the first molecules chemisorb flat on the surface and those added above about half a monolayer adopt a vertical orientation. All the adsorbed alkyl iodides decompose by 140 K via the scission of their C−I bond and generate alkyl groups on the surface. Those surface alkyls also change configuration with coverage, aligning themselves at saturation in a fashion reminiscence of that seen in self-assembled monolayers.
No takes yet. Share an insight, caveat, or question.
Jenks et al. (1999) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: