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A combined experimental and theoretical study on the reactivity of nitrenes and nitrene radical anions

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  • Yujing Guo

    (RWTH Aachen University)

  • Chao Pei

    (RWTH Aachen University)

  • Rene M. Koenigs

    (RWTH Aachen University)

Abstract

Nitrene transfer reactions represent one of the key reactions to rapidly construct new carbon-nitrogen bonds and typically require transition metal catalysts to control the reactivity of the pivotal nitrene intermediate. Herein, we report on the application of iminoiodinanes in amination reactions under visible light photochemical conditions. While a triplet nitrene can be accessed under catalyst-free conditions, the use of a suitable photosensitizer allows the access of a nitrene radical anion. Computational and mechanistic studies rationalize the access and reactivity of triplet nitrene and nitrene radical anion and allow the direct comparison of both amination reagents. We conclude with applications of both reagents in organic synthesis and showcase their reactivity in the reaction with olefins, which underline their markedly distinct reactivity. Both reagents can be accessed under mild reaction conditions at room temperature without the necessity to exclude moisture or air, which renders these metal-free, photochemical amination reactions highly practical.

Suggested Citation

  • Yujing Guo & Chao Pei & Rene M. Koenigs, 2022. "A combined experimental and theoretical study on the reactivity of nitrenes and nitrene radical anions," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-021-27687-6
    DOI: 10.1038/s41467-021-27687-6
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    1. Gong, Jiawei & Sumathy, K. & Qiao, Qiquan & Zhou, Zhengping, 2017. "Review on dye-sensitized solar cells (DSSCs): Advanced techniques and research trends," Renewable and Sustainable Energy Reviews, Elsevier, vol. 68(P1), pages 234-246.
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