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有机镍催化介导的硝酸盐升级循环利用

Nitrate Upcycling Mediated by Organonickel Catalysis.

作者信息

Padmanaban Sudakar, Chun Jeewon, Lee Youngseob, Cho Kyung-Bin, Choi Jonghoon, Lee Yunho

机构信息

Department of Chemistry, Seoul National University, Seoul, 08826, Republic of Korea.

Department of Chemistry and Research Institute of Physics and Chemistry, Jeonbuk National University, Jeonju, 54896, Republic of Korea.

出版信息

Angew Chem Int Ed Engl. 2024 Sep 23;63(39):e202408457. doi: 10.1002/anie.202408457. Epub 2024 Jul 17.

Abstract

Nitrogen oxides (NO) are major environmental pollutants and to neutralize this long-term environmental threat, new catalytic methods are needed. Although there are biological denitrification processes involving four different enzymatic reactions to convert nitrate (NO ) into dinitrogen (N), it is unfortunately difficult to apply in industry due to the complexity of the processes. In particular, nitrate is difficult to functionalize because of its chemical stability. Thus, there is no organometallic catalysis to convert nitrate into useful chemicals. Herein, we present a nickel pincer complex that is effective as a bifunctional catalyst to stepwise deoxygenate NO by carbonylation and further through C-N coupling. By using this nickel catalysis, nitrate salts can be selectively transformed into various oximes (>20 substrates) with excellent conversion (>90 %). Here, we demonstrate for the first time that the highly inert nitrate ion can be functionalized to produce useful chemicals by a new organonickel catalysis. Our results show that the NO conversion and utilization (NCU) technology is a successful pathway for environmental restoration coupled with value-added chemical generation.

摘要

氮氧化物(NO)是主要的环境污染物,为了消除这种长期的环境威胁,需要新的催化方法。尽管存在涉及四种不同酶促反应将硝酸盐(NO₃⁻)转化为氮气(N₂)的生物反硝化过程,但不幸的是,由于过程复杂,难以应用于工业。特别是,硝酸盐由于其化学稳定性而难以官能化。因此,不存在将硝酸盐转化为有用化学品的有机金属催化。在此,我们展示了一种镍钳形配合物,它作为双功能催化剂通过羰基化逐步使NO₃⁻脱氧,并进一步通过C-N偶联实现。通过使用这种镍催化,硝酸盐可以选择性地转化为各种肟(>20种底物),转化率优异(>90%)。在此,我们首次证明了高度惰性的硝酸根离子可以通过一种新的有机镍催化官能化以产生有用的化学品。我们的结果表明,NO转化与利用(NCU)技术是环境修复与增值化学品生成相结合的成功途径。

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