A Bench-Stable Fluorophosphine Nickel(0) Complex and Its Catalytic Application

Franziska Flecken, Arjun Neyyathala, Toni Grell, Schirin Hanf
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引用次数: 0

Abstract

We herein present a fluorophosphine-based nickel(0) complex [Ni(PFPh2)4] (1), which is highly stable in air and water. [Ni(PFPh2)4] can be obtained from a one-pot reaction of [Ni(MeCN)4](BF4)2 with Ph2P(═O)–PPh2, involving a unique in situ reduction of Ni(II) to Ni(0) and a simultaneous fluorination by the BF4 anion. This complex does not only incorporate a nickel center in the zero-oxidation state, resulting from a Ni(II) precursor, but also includes fluorophosphine ligands, which typically disproportionate immediately in solution. The application of [Ni(PFPh2)4] as highly stable Ni(0) pre-catalyst in combination with additional phosphine ligands, such as dppf (1,1′-bis(diphenylphosphino)ferrocene), in various coupling reactions uncovers its high catalytic activity and versatility, which is superior to [Ni(COD)2] (COD═cycloocta-1,5-diene) as conventional Ni(0) source.

一种稳定的氟膦镍配合物及其催化应用
本文提出了一种氟膦基镍(0)配合物[Ni(PFPh2)4](1),该配合物在空气和水中具有很高的稳定性。[Ni(PFPh2)4]可以由[Ni(MeCN)4](BF4)2与Ph2P(= O) -PPh2的一锅反应得到,包括Ni(II)在原位还原为Ni(0)和同时由BF4−阴离子氟化。该配合物不仅包含由Ni(II)前体产生的处于零氧化态的镍中心,而且还包括氟膦配体,其通常在溶液中立即不成比例。[Ni(PFPh2)4]作为高度稳定的Ni(0)预催化剂与附加的膦配体(如dppf(1,1 ' -双(二苯基膦)二茂铁)结合在各种偶联反应中的应用,揭示了它的高催化活性和多功能性,优于[Ni(COD)2] (COD =环-1,5-二烯)作为传统Ni(0)源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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1 months
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