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Synthetic Approaches for C-N Bonds by TiO2 Photocatalysis

机译:TiO2光催化合成C-N键的方法

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摘要

Nitrogen-containing organic compounds possess the most important status in drug molecules and agricultural chemicals. More than 80% currently used drugs have at least a C-N bond. The green and mild methodology to prepare diverse C-N bonds to replace traditional harsh preparation protocols is always a hotspot in modern synthetic chemistry. TiO2-based nanomaterials, considered as environmentally benign, stable, and powerful photocatalysts, have recently been applied in some certain challenging organic synthesis including construction of useful C-N compounds under mild conditions that are impossible to complete by conventional catalysis. This mini review would present state-of-the-art paragon examples of TiO2 photocatalyzed C-N bond formations. The discussion would be divided into two main sections: (1) N-alkylation of amines and (2) C-N formation in heterocycle synthesis. Especially, the mechanism of TiO2 photocatalytic C-N bond formation through activating alcohol into C=O by photo-induced hole followed by C=NH-R formation and finally hydrogenating C=NH-R into C-N bonds by combination of photo-induced electron/H+ assisted with loaded-Pt would be covered in detail. We believe that the mini-review will bring new insights into TiO2 photocatalysis applied to construct challenging organic compounds through enabling photo-induced hole and electron in a concerted way on coupling two substrate molecules together with respect to their conventionally independent catalysis behavior.
机译:含氮有机化合物在药物分子和农药中占有最重要的地位。目前超过80%的药物至少具有C-N键。制备多样的C-N键以取代传统的苛刻制备方案的绿色,温和的方法一直是现代合成化学的热点。基于TiO 2的纳米材料被认为对环境无害,稳定且功能强大,最近已用于某些具有挑战性的有机合成中,包括在温和条件下构建有用的C-N化合物,而这些条件是常规催化无法完成的。这篇小型综述将提供TiO2光催化C-N键形成的最新对等实例。讨论将分为两个主要部分:(1)胺的N-烷基化和(2)杂环合成中C-N的形成。尤其是通过光致空穴将醇活化成C = O,随后形成C = NH-R,最后通过光致电子/ H的结合使C = NH-R加氢成CN键,从而形成TiO2光催化CN键的机理。 + 结合有载Pt将被详细介绍。我们相信,此次迷你审查将通过使光致空穴和电子以协同方式将两个底物分子结合在一起,从而以传统方式独立的催化行为,为构造具有挑战性的有机化合物提供新的见解。

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