Mechanistic Investigation and Optimization of Photoredox Anti-Markovnikov Hydroamination

Yangzhong Qin, Qilei Zhu, Rui Sun, Jacob M. Ganley, Robert R. Knowles, Daniel G. Nocera

Research output: Contribution to journalArticlepeer-review

29 Scopus citations


The reaction mechanism and the origin of the selectivity for the photocatalytic intermolecular anti-Markovnikov hydroamination of unactivated alkenes with primary amines to furnish secondary amines have been revealed by time-resolved laser kinetics measurements of the key reaction intermediates. We show that back-electron transfer (BET) between the photogenerated aminium radical cation (ARC) and reduced photocatalyst complex (Ir(II)) is nearly absent due to rapid deprotonation of the ARC on the sub-100 ns time scale. The selectivity for primary amine alkylation is derived from the faster addition of the primary ARCs (as compared to secondary ARCs) to alkenes. The turnover of the photocatalyst occurs via the reaction between Ir(II) and a thiyl radical; the in situ formation of an off-cycle disulfide from thiyl radicals suppresses this turnover, diminishing the efficiency of the reaction. With these detailed mechanistic insights, the turnover of the photocatalyst has been optimized, resulting in a >10-fold improvement in the quantum yield. These improvements enabled the development of a scalable flow protocol, demonstrating a potential strategy for practical applications with improved energy efficiency and cost-effectiveness.

Original languageEnglish (US)
Pages (from-to)10232-10242
Number of pages11
JournalJournal of the American Chemical Society
Issue number27
StatePublished - Jul 14 2021

All Science Journal Classification (ASJC) codes

  • General Chemistry
  • Biochemistry
  • Catalysis
  • Colloid and Surface Chemistry


Dive into the research topics of 'Mechanistic Investigation and Optimization of Photoredox Anti-Markovnikov Hydroamination'. Together they form a unique fingerprint.

Cite this