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Updated: Jun 17, 2026

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
Taming the captodative glycyl radical for nickel-photocatalytic cross-coupling with alkyl chlorides
Rani Kumari1, Ning Wei1,2, Sebastian B Beil1,2
1Max-Planck-Institute for Chemical Energy Conversion, Department of Electrosynthesis, Stiftstr. 34-36, 45470, Mülheim an der Ruhr, Germany. sebastian.beil@cec.mpg.de.
Abstract:
The captodatively stabilized glycyl radical was engaged in nickel photocatalysed C(sp3)-C(sp3) cross-coupling to obtain non-canonical amino acids. DFT-guided optimization of the amine protecting groups allowed for radical destabilization and tuning of its SOMO-LUMO gap. Optimization and control experiments highlight a radical cross-coupling mechanism.
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