Oxidative Addition and Reductive Elimination at Main-Group Element Centers

被引:463
作者
Chu, Terry [1 ]
Nikonov, Georgii I. [1 ]
机构
[1] Brock Univ, Dept Chem, 1812 Sir Isaac Brock Way, St Catharines, ON L2S 3A1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
H BOND ACTIVATION; N-HETEROCYCLIC CARBENES; ABSOLUTE RATE CONSTANTS; METAL-FREE ACTIVATION; TERMINAL CHALCOGENIDO COMPLEXES; AL(2P)(SIH4) REVERSIBLE SIH3ALH; STABLE SINGLET CARBENES; X-RAY STRUCTURES; FACILE C-H; P-P BONDS;
D O I
10.1021/acs.chemrev.7b00572
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxidative addition and reductive elimination are key steps in a wide variety of catalytic reactions mediated by transition-metal complexes. Historically, this reactivity has been considered to be the exclusive domain of d-block elements. However, this paradigm has changed in recent years with the demonstration of transition-metal-like reactivity by main-group compounds. This Review highlights the substantial progress achieved in the past decade for the activation of robust single bonds by main group compounds and the more recently realized activation of multiple bonds by these elements. We also discuss the significant discovery of reversible activation of single bonds and distinct examples of reductive elimination at main-group element centers. The review consists of three major parts, starting with oxidative addition of single bonds, proceeding to cleavage of multiple bonds, and culminated by the discussion of reversible bond activation and reductive elimination. Within each subsection, the discussion is arranged according to the type of bond being cleaved or formed and considers elements from the left to the right of each period and down each group of the periodic table. The majority of results discussed in this Review come from the past decade; however, earlier reports are also included to ensure completeness.
引用
收藏
页码:3608 / 3680
页数:73
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