Gold π-Complexes as Model Intermediates in Gold Catalysis

被引:33
|
作者
Jones, Amanda C. [1 ]
机构
[1] Wake Forest Univ, Winston Salem, NC 27109 USA
来源
HOMOGENEOUS GOLD CATALYSIS | 2015年 / 357卷
基金
美国国家科学基金会;
关键词
pi-System (alkene/alkyne/allene) activation; Gold catalysis; Ligand effects; Mechanism; Reactivity; DYNAMIC SOLUTION BEHAVIOR; RAY CRYSTAL-STRUCTURES; ION-PAIR STRUCTURE; STRUCTURAL-CHARACTERIZATION; GOLD(I)-CATALYZED HYDROALKOXYLATION; COORDINATION CHEMISTRY; ORGANOGOLD COMPLEXES; ALKENE COMPLEXES; ALKYNE COMPLEXES; TERMINAL ALKYNES;
D O I
10.1007/128_2014_593
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Homogeneous gold catalysis has emerged as a powerful method for activating hydrocarbon double and triple bonds. Methodology development and computational studies have blossomed in the past 20 years. In contrast, experimental exploration of mechanisms and structure-reactivity relationships has gained traction only in the past 5 years. Recent developments in the synthesis of organometallic intermediates have revealed exciting new details about the mechanisms of gold catalysis. Central to these studies are the structure and reactivity of gold p-complexes. Following successes in structurally characterizing these key structures, advancements are gradually being made in placing them in the context of an overall catalytic cycle. As a result, a research field has emerged which is rich with potential for continued discovery and catalyst improvement.
引用
收藏
页码:133 / 165
页数:33
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