Molecular hydrogenolysis

Single-bond cleavage with molecular hydrogen is termed hydrogenolysis. Palladium is the best catalyst for this purpose, platinum is not useful. Desulfurizations are most efficiently per-formed with Raney nickel (with or without hydrogen G.R. Pettit, 1962 A or with alkali metals in liquid ammonia or amines. The scheme below summarizes some classes of compounds most susceptible to hydrogenolysis. 

Note that, while this reaction (as well as alkane hydrogenolysis) involves known elementary steps of molecular organometallic chemistry, it has not been discovered in homogeneous catalysis. One reason might be that highly... 

Additionally, grafting molecular entities on surfaces has already allowed to discover several reactions the low temperature hydrogenolysis of alkanes including the depolymerization of polyolefins, the alkane metathesis and the cross-metathesis of methane and alkanes. These two latter reactions can allow higher molecular weight alkanes to be built. 

We have studied the hydrogenolysis of 2-(perfluorohexyl)ethane thiocyanate to 2-(perfluorohexyl)ethane thiol. It was discovered that perfluoroalkyl thiocyanates can be reduced to thiols and co-product hydrogen cyanide with molecular hydrogen in the presence of a carbon-supported palladium-tin catalyst. This result is surprising since it is known that palladium and other gronps 8 to 10 metal catalysts are poisoned by the product thiol, traces of hydrogen snlfide byprodnct, and the hydrogen cyanide co-product. For that reason, we characterized the catalyst to understand why it was so robust under conditions that would normally poison snch a catalyst. 

Now, since each respective fraction shows a structural change along with the reaction course, it may be considered at the same time that it contains products from a higher molecular fraction. In other words, for instance i r A2 is produced from coal 2 which changes by hydrogenolysis and at the same time, the residue resultinq from the reaction from Fr Ai to Fr also appears in this fraction. 

Schultz and Linden Ind. Eng. Chem. Process Design and Development, 1 (111), 1962] have studied the hydrogenolysis of low molecular weight paraffins in a tubular flow reactor. The kinetics of the propane reaction may be assumed to be first-order in propane in the regime of interest. From the data below determine the reaction rate constants at the indicated temperatures and the activation energy of the reaction. 

A reacting molecule has, as an alternative to isomerization, reaction by hydrogenolysis in which lower molecular weight products are formed. This latter process will be discussed in detail in a subsequent section. However, we note here that the relative importance of isomerization versus hydrogenolysis decreases as the partial pressure of hydrogen in the reaction mixture increases. This has been demonstrated by Kikuchi et al. 128) for... 

Reductive animation of aromatic aldehydes to give benzylamines is accomplished by heating the aldehyde and tritylamine with molecular sieves, followed by the addition of sodium cyanoborohydride. Catalytic hydrogenolysis of the products with palladium on charcoal yields the benzylamines (equation 56)167. 

Reaction of 3,3-disubstituted-l,4-pentadiene 92 with a primary amine under cyclohydrocarbonylation conditions yielded cyclopenta[. ]pyrrole 96 as the predominant product accompanied by a small amount of cyclopentanone 95 (Scheme 15). This unique reaction is proposed to proceed through a cascade hydrocarbonylation-carbonylation process. The first hydrocarbonylation of 92 and the subsequent carbocyclization formed cyclopentanoylmethyl-Rh complex 93. If 93 immediately reacts with molecular hydrogen, 2-methylcyclopentanone 95 is formed. However, if CO insertion takes place faster than the hydrogenolysis, cyclopentanoylacetyl-Rh complex 94 is generated, which undergoes the Paal-Knorr condensation with a primary amine to yield cyclopenta[. ]pyrrole 96. ... 

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