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催化磷属元素键形成反应脱氢偶联和氢官能化的最新进展。

Recent advances in catalytic pnictogen bond forming reactions dehydrocoupling and hydrofunctionalization.

机构信息

University of Vermont, Department of Chemistry, 82 University Place, Burlington, Vermont, USA.

出版信息

Chem Commun (Camb). 2023 Jan 31;59(10):1258-1273. doi: 10.1039/d2cc06143k.

Abstract

An examination of several catalytic reactions among the group 15 elements is presented. The connections between the chemistry of the pnictogens can sometimes be challenging, but aspects of metal-pnictogen reactivity are the key. The connecting reactivity comes from metal-catalyzed transformations such as dehydrocoupling and hydrofunctionalization. Pivotal mechanistic insights from E-N heterodehydrocoupling have informed the development of highly active catalysts for these reactions. Metal-amido nucleophilicity is often at the core of this reactivity, which diverges from phosphine and arsine dehydrocoupling. Nucleophilicity connects to the earliest understanding of hydrophosphination catalysis, but more recent catalysts are leveraging enhanced insertion activity through photolysis. This photocatalysis extends to hydroarsination, which may also have more metal-arsenido nucleophilicity than anticipated. However, metal-catalyzed arsinidene chemistry foreshadowed related phosphinidene chemistry by years. This examination shows the potential for greater influence of individual discoveries and understanding to leverage new advances between these elements, and it also suggests that the chemistry of heavier elements may have more influence on what is possible with lighter elements.

摘要

本文介绍了第 15 族元素之间的几种催化反应。磷属元素的化学性质有时可能具有挑战性,但金属-磷属元素反应性的某些方面是关键。连接反应性来自于金属催化的转化,如脱氢偶联和氢官能化。E-N 杂脱氢偶联的关键机理见解为这些反应的高效催化剂的发展提供了信息。金属-酰胺亲核性通常是这种反应性的核心,它与膦和胂的脱氢偶联不同。亲核性与最早的氢膦化催化理解联系在一起,但最近的催化剂通过光解利用增强的插入活性。这种光催化扩展到氢胂化,其可能具有比预期更多的金属-胂基亲核性。然而,金属催化的砷烯化学预示着相关的磷烯化学提前了数年。本文的研究表明,个别发现和理解的更大影响有可能在这些元素之间利用新的进展,并且还表明较重元素的化学性质可能对较轻元素的可能性有更大的影响。

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