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氢化元素加成与磷烯转移:磷锗烯和磷锡烯对小分子底物的反应活性

Hydroelementation and Phosphinidene Transfer: Reactivity of Phosphagermenes and Phosphastannenes Towards Small Molecule Substrates.

作者信息

Reveley Matthew J, Feld Joey, Temerova Diana, Yang Eric S, Goicoechea Jose M

机构信息

Department of Chemistry, University of Oxford Chemistry Research Laboratory, 12 Mansfield Rd., Oxford, OX1 3TA, UK.

Department of Chemistry, Indiana University, 800 E. Kirkwood Ave., Bloomington, IN., 47405, USA.

出版信息

Chemistry. 2023 Dec 6;29(68):e202301542. doi: 10.1002/chem.202301542. Epub 2023 Oct 9.

Abstract

We describe the facile synthesis of [(Me Si) CH] E=PMes* (E=Ge, Sn) from the reaction of the tetrylenes with the phospha-Wittig reagent, Me P-PMes*. Their reactivity towards a range of substrates with protic and hydridic E-H bonds (E=N, O, Si) is described. In addition to hydroelementation reactions of the E=P bonds, we show that these compounds, particularly [(Me Si) CH] Sn=PMes*, also act as base-stabilized phosphinidenes, allowing phosphinidene transfer to other nucleophiles.

摘要

我们描述了通过四价元素与磷叶立德试剂MeP-PMes反应,简便合成[(MeSi)CH]E=PMes(E=Ge、Sn)的方法。描述了它们对一系列带有质子型和氢型E-H键(E=N、O、Si)底物的反应活性。除了E=P键的氢元素加成反应外,我们还表明这些化合物,特别是[(MeSi)CH]Sn=PMes*,也可作为碱稳定的磷烯,能将磷烯转移至其他亲核试剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc16/10946619/5676977538c9/CHEM-29-0-g006.jpg

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