Markovnikov-selective double hydrosilylation of challenging terminal aryl alkynes under cobalt and iron catalysis

Geminal bis(silanes) are unique compounds with interesting properties. The most straightforward way to access them is double hydrosilylation of alkynes, which was established only recently. Previous articles about transition metal-catalysed double hydrosilylation show that terminal aryl alkynes are a challenge. We report on cobalt( ii ) and iron( iii ) complexes with the easy-to-synthesise N , N , N -tridentate hydrazone ligand being active precatalysts in Markovnikov-selective double hydrosilylation of terminal aryl alkynes. The influence of the hydrazone ligand structure and the potential role of the sodium triethylborohydride activator were studied. Sets of geminal bis(silanes) with two identical or different silyl groups were synthesised, showing the applicability of the reported method. Bench-stable complexes with a tridentate ligand serve as precatalysts in the synthesis of geminal bis(silanes) from terminal aryl alkynes regarded as challenging substrates in this transformation.