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在交叉偶联反应中对硝酮基氮氧化物金衍生物进行超频。

Overclocking Nitronyl Nitroxide Gold Derivatives in Cross-Coupling Reactions.

作者信息

Zayakin Igor, Tretyakov Evgeny, Akyeva Anna, Syroeshkin Mikhail, Burykina Julia, Dmitrenok Andrey, Korlyukov Alexander, Nasyrova Darina, Bagryanskaya Irina, Stass Dmitri, Ananikov Valentine

机构信息

N. D. Zelinsky Institute of Organic Chemistry, 47 Leninsky Prosp., 119991, Moscow, Russia.

A. N. Nesmeyanov Institute of Organoelement Compounds, 28 Vavilov Str., 119991, Moscow, Russia.

出版信息

Chemistry. 2023 Jan 27;29(6):e202203118. doi: 10.1002/chem.202203118. Epub 2022 Dec 7.

Abstract

Nitronyl nitroxides are functional building blocks in cutting-edge research fields, such as the design of molecular magnets, the development of redox and photoswitchable molecular systems and the creation of redox-active components for organic and hybrid batteries. The key importance of the nitronyl nitroxide function is to translate molecular-level-optimized structures into nano-scale devices and new technologies. In spite of great importance, efficient and versatile synthetic approaches to these compounds still represent a challenge. Particularly, methods for the direct introduction of a nitronyl nitroxide moiety into aromatic systems possess many limitations. Here, we report gold derivatives of nitronyl nitroxide that can enter Pd(0)-catalysed cross-coupling reactions with various aryl bromides, affording the corresponding functionalized nitronyl nitroxides. Based on the high thermal stability and enhanced reactivity in catalytic transformation, a new reagent is suggested for the synthesis of radical systems via a universal cross-coupling approach.

摘要

硝酮氮氧化物是前沿研究领域中的功能性构建单元,例如分子磁体的设计、氧化还原和光开关分子体系的开发以及有机和混合电池中氧化还原活性成分的创制。硝酮氮氧化物功能的关键重要性在于将分子水平优化的结构转化为纳米级器件和新技术。尽管非常重要,但高效且通用的这些化合物的合成方法仍然是一项挑战。特别是,将硝酮氮氧化物部分直接引入芳族体系的方法存在许多局限性。在此,我们报道了硝酮氮氧化物的金衍生物,其可与各种芳基溴化物发生钯(0)催化的交叉偶联反应,得到相应的功能化硝酮氮氧化物。基于高热稳定性和催化转化中增强的反应性,提出了一种通过通用交叉偶联方法合成自由基体系的新试剂。

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