Cyclopentadienyl ring activation in organometallic chemistry and catalysis

被引:8
|
作者
VanderWeide, Andrew [1 ]
Prokopchuk, Demyan E. E. [1 ]
机构
[1] Rutgers State Univ, Dept Chem, Newark, NJ 07102 USA
基金
美国国家科学基金会;
关键词
METAL-PI-COMPLEXES; C-H ACTIVATION; SANDWICH COMPLEXES; ELECTRON-TRANSFER; PROTON REDUCTION; IRON COMPLEXES; CO2; REDUCTION; ACTIVE-SITE; LIGAND; HYDROGEN;
D O I
10.1038/s41570-023-00501-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The cyclopentadienyl (Cp) ligand is a cornerstone of modern organometallic chemistry. Since the discovery of ferrocene, the Cp ligand and its various derivatives have become foundational motifs in catalysis, medicine and materials science. Although largely considered an ancillary ligand for altering the stereoelectronic properties of transition metal centres, there is mounting evidence that the core Cp ring structure also serves as a reservoir for reactive protons (H+), hydrides (H-) or radical hydrogen (H-center dot) atoms. This Review chronicles the field of Cp ring activation, highlighting the pivotal role that Cp ligands can have in electrocatalytic H-2 production, N-2 reduction, hydride transfer reactions and proton-coupled electron transfer.
引用
收藏
页码:561 / 572
页数:12
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