Abstract
Si–O and Si–N heterodehydrocoupling catalyzed by the commercially available iron dimer (1)
under photochemical conditions is reported. Mechanistic study reveals
that the most immediate hurdle in the catalysis is the poor activation
of 1, demonstrating the necessity to fully activate the catalyst to realize the potential of iron in this reactivity.
Supplementary materials
Title
SI Fp SiO SiN FINAL
Description
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