4.8 Article

Nickel-Catalyzed NO Group Transfer Coupled with NOx Conversion

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 10, Pages 4585-4593

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c13560

Keywords

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Funding

  1. National Research Foundation of Korea [2018R1A5A1025208, 2020R1A2C3007364, 2021R1A2C1012851]
  2. C1 Gas Refinery Program [NRF 2021M3D3A1A01022098]
  3. National Research Foundation of Korea [2021R1A2C1012851, 2020R1A2C3007364] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study presents a synthetic approach to the conversion of NOx utilizing a bifunctional metal catalyst, which effectively converts Ni-NOx to Ni-NO and transfers the nitroso group to organic substrates. The successful catalytic production of oximes from benzyl halides using NaNO2 as a substrate is achieved under mild conditions.
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)-N-center dot 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.

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