A new approach to studying the mechanism of catalytic reactions: An investigation into the photocatalytic hydrogenation of norbornadiene and dimethylfumarate using polyethylene matrices at low temperature and high pressure

G. I. Childs, A. I. Cooper, T. F. Nolan, M. J. Carrott, M. W. George, M. Poliakoff

Research output: Journal PublicationArticlepeer-review

37 Citations (Scopus)

Abstract

This paper presents a new method for investigating the mechanisms of homogeneously catalyzed reactions involving gases, particularly H2. 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)42-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)42-DF) in a PE matrix at 150 K resulted in the formation of an intermediate complex tentatively assigned Fe(CO)34-DF). Warming this complex to 260 K under H2 leads to the formation of Fe(CO)32-DF)(η2-H2). 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 H2 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 H2 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 H2 and D2. 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.

Original languageEnglish
Pages (from-to)6857-6866
Number of pages10
JournalJournal of the American Chemical Society
Volume123
Issue number28
DOIs
Publication statusPublished - 2001
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • Chemistry (all)
  • Biochemistry
  • Colloid and Surface Chemistry

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