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. 2018 Mar 12;9(15):3759–3766. doi: 10.1039/c7sc05313d

Fig. 1. Temperature programmed experiments show nearly complete displacement of acetate by trifluoroacetic acid on Au(110) at 300 K. (A) The characteristic products for reaction of 0.10 ML of isolated trifluoroacetate (red) decomposed to CF3 and CO2 at 590 K, while 0.10 ML of isolated acetate (blue) decomposed to CO2 and CH3 at 580 K. (B) The introduction of (i) excess trifluoroacetic acid to acetate and (ii) excess acetic acid to trifluoroacetate yields products characteristic of a majority species trifluoroacetate and a minority species acetate. The deconvolution of the CO2 peak for acetate (blue) and trifluoroacetate (red) is determined by using a selectivity fraction on the CH3 and CF3 peaks. Both orders of adsorption show displacement that favors trifluoroacetate.

Fig. 1