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Nickel-Catalyzed NO Group Transfer Coupled with NOxConversion

  • Sudakar Padmanaban
  • , Jonghoon Choi
  • , Hugo Vazquez-Lima
  • , Donghwi Ko
  • , Dagyum Yoo
  • , Jinseong Gwak
  • , Kyung Bin Cho*
  • , Yunho Lee*
  • *Corresponding author for this work
  • Seoul National University
  • Jeonbuk National University
  • Korea Advanced Institute of Science and Technology

Research output: Contribution to journalJournal articlepeer-review

Abstract

Nitrogen oxide (NOx) conversion is an important process for balancing the global nitrogen cycle. Distinct from the biological NOx transformation, we have devised a synthetic approach to this issue by utilizing a bifunctional metal catalyst for producing value-added products from NOx. Here, we present a novel catalysis based on a Ni pincer system, effectively converting Ni-NOx to Ni-NO via deoxygenation with CO(g). This is followed by transfer of the in situ generated nitroso group to organic substrates, which favorably occurs at the flattened Ni(I)-NO site via its nucleophilic reaction. Successful catalytic production of oximes from benzyl halides using NaNO2 is presented with a turnover number of >200 under mild conditions. In a key step of the catalysis, a nickel(I)-•NO species effectively activates alkyl halides, which is carefully evaluated by both experimental and theoretical methods. Our nickel catalyst effectively fulfills a dual purpose, namely, deoxygenating NOx anions and catalyzing C-N coupling.

Original languageEnglish
Pages (from-to)4585-4593
Number of pages9
JournalJournal of the American Chemical Society
Volume144
Issue number10
DOIs
StatePublished - 2022.03.16

Quacquarelli Symonds(QS) Subject Topics

  • Engineering - Petroleum
  • Engineering - Chemical
  • Chemistry
  • Biological Sciences

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