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高价镍物种介导的需氧碳-碳和碳-氧键形成反应。

Aerobic C-C and C-O bond formation reactions mediated by high-valent nickel species.

作者信息

Smith Sofia M, Planas Oriol, Gómez Laura, Rath Nigam P, Ribas Xavi, Mirica Liviu M

机构信息

Department of Chemistry , Washington University in St. Louis , One Brookings Drive , St. Louis , Missouri 63130-4899 , USA.

Departament de Química , Institut de Química Computacional i Catàlisi (IQCC) , Universitat de Girona , Campus de Montilivi , Girona E-17003 , Catalonia , Spain.

出版信息

Chem Sci. 2019 Sep 24;10(44):10366-10372. doi: 10.1039/c9sc03758f. eCollection 2019 Nov 28.

Abstract

Nickel complexes have been widely employed as catalysts in C-C and C-heteroatom bond formation reactions. While Ni(0), Ni(i), and Ni(ii) intermediates are most relevant in these transformations, recently Ni(iii) and Ni(iv) species have also been proposed to play a role in catalysis. Reported herein is the synthesis, detailed characterization, and reactivity of a series of Ni(ii) and Ni(iii) metallacycle complexes stabilized by tetradentate pyridinophane ligands with various N-substituents. Interestingly, while the oxidation of the Ni(ii) complexes with various other oxidants led to exclusive C-C bond formation in very good yields, the use of O or HO as oxidants led to formation of appreciable amounts of C-O bond formation products, especially for the Ni(ii) complex supported by an asymmetric pyridinophane ligand containing one tosyl N-substituent. Moreover, cryo-ESI-MS studies support the formation of several high-valent Ni species as key intermediates in this uncommon Ni-mediated oxygenase-type chemistry.

摘要

镍配合物已被广泛用作碳-碳和碳-杂原子键形成反应的催化剂。虽然Ni(0)、Ni(I)和Ni(II)中间体在这些转化中最为相关,但最近也有人提出Ni(III)和Ni(IV)物种在催化过程中发挥作用。本文报道了一系列由具有各种N-取代基的四齿吡啶环配体稳定的Ni(II)和Ni(III)金属环配合物的合成、详细表征及反应活性。有趣的是,虽然用各种其他氧化剂氧化Ni(II)配合物会以非常高的产率专一性地形成碳-碳键,但使用O₂或H₂O₂作为氧化剂会导致形成相当数量的碳-氧键形成产物,特别是对于由含有一个甲苯磺酰基N-取代基的不对称吡啶环配体支持的Ni(II)配合物。此外,低温电喷雾电离质谱研究支持形成几种高价镍物种作为这种不常见的镍介导的加氧酶型化学反应中的关键中间体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2984/6984385/5da62beb9c98/c9sc03758f-s1.jpg

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