Hydrogen exposure effects on Pt/Al2O3 catalysts coated with thiolate monolayers.

Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) was used to examine the effect of thermal treatment of self-assembled monolayers (SAMs) produced from various thiols (1-hexanethiol, 1-decanethiol, 1-octadecanethiol, 1,6-hexanedithiol, 1,10-decanedithiol, 1,2-benzenedithiol) on a 5 wt % Pt/Al2O3 catalyst. Catalysts were characterized during heating and cooling between 290 and 553 K in both the presence and absence of H2. Overall, the behavior of thiols on Pt/Al2O3 in an inert He environment was similar to the behavior reported in other works on Au, although in the case of the Pt catalyst, C-H bond dissociation in the thiols was apparent at high temperatures. Under H2 flow, however, markedly different behavior was observed; in particular, conformational order was observed to increase with increasing temperature, up to temperatures as high as 500 K for octadecanethiol-coated catalysts. The effects of H2 exposure are much less pronounced for alkanedithiol-coated catalysts. 1,2-Benzenedithiol was found to undergo partial hydrogenation under H2, indicating that hydrogenating reaction conditions can also influence the chemical structure of the monolayer on active metals, such as Pt. The differences in thiolate structure caused by high-temperature exposure to hydrogen were found to have a significant effect on the rate and selectivity for hydrogenation of prenal, indicating that such effects may be broadly important in the use of thiolate-promoted catalysts for hydrogenation reactions.

Analysis of lipids: metal oxide laser ionization mass spectrometry.

Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has been used for lipid analysis; however, one of the drawbacks of this technique is matrix interference peaks at low masses. Metal oxide surfaces are described here for direct, matrix-free analysis of small (MW < 1000 Da) lipid compounds, without interferences in the resulting spectra from traditional matrix background peaks. Spectra from lipid standards produced protonated and sodiated molecular ions. More complex mixtures including vegetable oil shortening and lipid extracts from bacterial and algal sources provided similar results. Mechanistic insight into the mode of ionization from surface spectroscopy, negative ion mass spectrometry, and stable isotope studies is also presented. The metal oxide system is compared to other reported matrix-free systems.