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The process contrasts with homogeneous catalysis where the reagents, products and catalyst exist in the same phase. Phase distinguishes between not only solid, liquid, and gas components, but also immiscible mixtures (e.g., oil and water), or anywhere an interface is present.
In chemistry, homogeneous catalysis is catalysis where the catalyst is in same phase as reactants, principally by a soluble catalyst in a solution. In contrast, heterogeneous catalysis describes processes where the catalysts and substrate are in distinct phases, typically solid and gas, respectively. [ 1 ]
Aspects are described in an early review: "using a non-protic Lewis acid, aluminium tribromide, were able to demonstrate the truly catalytic effect of titanium by treating dinitrogen with a mixture of titanium tetrachloride, metallic aluminium, and aluminium tribromide at 50 °C, either in the absence or in the presence of a solvent, e.g. benzene.
Homogeneous metallocene catalysts, e.g., derived from or related to zirconocene dichloride introduced a level of microstructural control that was unavailable with heterogeneous systems. [2] Metallocene catalysts are homogeneous single-site systems, implying that a uniform catalyst is present in the solution. In contrast, commercially important ...
This reactor is typically used when one reactant is a gas and the other a liquid while the catalyst is a solid. The reactant gas is put through the liquid and dissolved. It then diffuses onto the catalyst surface. Slurry reactors can use very fine particles and this can lead to problems of separation of catalyst from the liquid.
A second class of Ziegler–Natta catalysts are soluble in the reaction medium. Traditionally such homogeneous catalysts were derived from metallocenes, but the structures of active catalysts have been significantly broadened to include nitrogen-based ligands. A post-metallocene catalyst developed at Dow Chemical. [8]
Additionally, when catalyst loadings are lower than 10 ppm – the regulatory limit for several metals including Pd in pharmaceutical APIs – separation of the metal following the reaction does not even need to be performed. This nullifies another of the commonly perceived advantages of heterogeneous catalysts over their homogeneous counterparts.
The final step is reductive elimination of the two coupling fragments to regenerate the catalyst and give the organic product. Unsaturated substrates, such as C(sp)−X and C(sp 2)−X bonds, couple more easily, in part because they add readily to the catalyst.