| Abstract
| - A series of meso-tetrakis(SCS-pincer PdCl)−(metallo)porphyrin hybrids have been synthesized using two distinct synthetic routes. Manganese and nickel were introduced into the porphyrin macrocycle prior to peripheral electrophilic palladation, whereas magnesium was introduced thereafter in light of its acid sensitivity. When these complexes were used as precatalysts in the Heck reaction between iodobenzene and styrene, different catalytic activities were observed for each hybrid complex. The catalytic activity increased for the metalloporphyrin series MnCl < 2H < Ni < Mg, which interestingly coincides with an increase of electron richness of the porphyrin ring. Control experiments on model compounds confirmed that an intramolecular effect rather than an intermolecular effect was responsible for this influence. We postulate that, in analogy with related NCN-pincer metal complexes, the electron density on the palladium atom in SCS-pincer palladium complexes is influenced by the electronic properties of the para-substituent, i.e., the metalloporphyrin in this case. This in turn influences the rate of palladium leaching and, hence, of catalysis.
- SCS-pincer-type palladium complexes were merged with (metallo)tetraphenylporphyrins to give heteromultimetallic compounds, which, when used as catalyst precursors in the Heck reaction between iodobenzene and styrene, exhibited different catalytic activities depending on the metal in the porphyrin cavity.
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