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Easy Access to Phosphine-Borane Building Blocks.
Chemistry - A European Journal ( IF 4.3 ) Pub Date : 2020-06-30 , DOI: 10.1002/chem.202002367
G Bas de Jong 1, 2 , Nuria Ortega 2 , Martin Lutz 3 , Koop Lammertsma 2, 4 , J Chris Slootweg 1, 2
Affiliation  

In this paper, we highlight the synthesis of a variety of primary phosphine‐boranes (RPH2⋅BH3) from the corresponding dichlorophosphines, simply by using Li[BH4] as reductant and provider of the BH3 protecting group. The method offers facile access not only to alkyl‐ and arylphosphine‐boranes, but also to aminophosphine‐boranes (R2NPH2⋅BH3) that are convenient building blocks but without the protecting BH3 moiety thermally labile and notoriously difficult to handle. The borane‐protected primary phosphines can be doubly deprotonated using n‐butyllithium to provide soluble phosphanediides Li2[RP⋅BH3] of which the phenyl‐derivative Li2[PhP⋅BH3] was structurally characterized in the solid state.

中文翻译:

轻松获取磷化硼烷积木。

在本文中,我们重点介绍了通过使用 Li[BH 4 ] 作为还原剂和 BH 3保护基的提供者,从相应的二氯膦合成各种伯膦硼烷 (RPH 2 ⋅BH 3 ) 。该方法不仅可以轻松获得烷基和芳基膦硼烷,还可以轻松获得氨基膦硼烷(R 2 NPH 2 ⋅BH 3),它们是方便的构建单元,但没有保护性的 BH 3部分,热不稳定且非常难以处理。硼烷保护的伯膦可以使用丁基锂进行双重去质子化,得到可溶性膦二化合物 Li 2 [RP⋅BH 3 ],其中苯基衍生物 Li 2 [PhP⋅BH 3 ] 具有固态结构特征。
更新日期:2020-06-30
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