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This paper presents a new method for investigating the mechanisms of homogeneously catalyzed reactions involving gases, particularly H 2 . We show how the combination of polyethylene (PE) matrices and high pressure-low temperature (HPLT) experiments can be used to provide new mechanistic information on hydrogenation processes. In particular, we show how we are able to generate reaction intermediates at low temperature, and then to extract the contents of the PE film at room temperature to characterize the organic products using GC-MS. We have used our new technique to probe both the hydrogenation of dimethyl fumarate (DF), using Fe(CO) 4 (η 2 -DF) as the catalytic species, and the hydrogenation of norbornadiene (NBD), using (NBD)M(CO) 4 (M ) Cr or Mo) as the catalytic species. Irradiation of Fe(CO) 4 (η 2 -DF) in a PE matrix at 150 K resulted in the formation of an intermediate complex tentatively assigned Fe(CO) 3 (η 4 -DF). Warming this complex to 260 K under H 2 leads to the formation of Fe(CO) 3 (η 2 -DF)(η 2 -H 2 ). Further warming of the reaction system results in the hydrogenation of the coordinated DF, to generate dimethyl succinate (DS). Characterization of the intermediate species was obtained using FTIR spectroscopy. Formation of DS was confirmed using both FTIR spectroscopy and GC-MS analysis. UV photolysis of (NBD)M(CO) 4 in PE under H 2 in the presence of excess NBD results in the formation of the hydrogenated products norbornene (NBN) and nortricyclene (NTC), with trace amounts of norbornane (NBA) being observed. These products were in similar ratios to those observed in fluid solution. However, for (NBD)Mo(CO) 4 , the relative amounts of the organic products change considerably when the reaction is repeated in PE under H 2 in the absence of free NBD, with NBA being the major product. The use of our HPLT cell allows us to vent and exchange high pressures of gases with ease, and as such we have performed gas exchange reactions with H 2 and D 2 . Analysis of the reaction products from these exchange reactions with GC-MS provides evidence for the mechanism of formation of NBA, in both the presence and absence of excess NBD, a reaction which has been largely ignored in previous studies.

Packed-column supercritical fluid chromatography (pSFC), with negative-ion atmospheric-pressure chemical-ionisation (APCI) mass spectrometric (MS) detection has been used to analyse a commercial phenol-formaldehyde (resol) prepolymer. After initial optimisation of the system using a standard dimer species [bis(2-hydroxyphenyl)methane], it was possible to identify positively 34 components in the resin sample, including the starting reagents (phenol and cresol), and a range of dimers, trimers, tetramers and pentamers, with varying phenol/cresol ratios and amounts of methylol substitution. The method requires no pre-separation derivatisation of the resin sample, and a chromatographic run time of ca. 10 min.