Carbon–carbon bond formation promoted by electrophiles and the mechanism of the Fischer–Tropsch reaction
Abstract
Decomposition of trans-[(C5Me5RhMe)2(µ-CH2)2] takes place at 20 °C in the presence of 1-electron oxidisers to give methane, ethylene, and notably propylene, by coupling of C1 ligands (thermally the same reactions only occur at 250 °C); the analogy to Fischer–Tropsch reactions on rhodium surface is noted.