Synthesis of Well-Defined High-Valent Palladium Complexes by Oxidation of Their Palladium(II) Precursors

被引:14
|
作者
Zhang, Bo [1 ]
Yan, Xuechao [1 ]
Guo, Shuai [1 ]
机构
[1] Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China
基金
中国国家自然科学基金;
关键词
electrooxidation; high-valent; oxidation; oxidation states; palladium; FORMING REDUCTIVE ELIMINATION; C-H ACTIVATION; RAY CRYSTAL-STRUCTURES; DINUCLEAR PALLADIUM(III); BOND-FORMATION; PD-IV; ORGANOMETALLIC PD(II); AEROBIC OXIDATION; CATALYTIC CYCLE; LIGAND;
D O I
10.1002/chem.202001074
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The last decade has witnessed the rapid development of high-valent Pd-involved organic transformations. This has also led to a steadily growing number of publications concerning the preparation of isolable and characterizable palladium(III) and palladium(IV) complexes. A variety of one-electron and two-electron oxidants have been employed to give access to high-oxidation-state Pd compounds. Undoubtedly, the study of these stoichiometric reactions has great implications for relevant Pd-mediated catalysis. In this minireview, the focus is on the synthetic approaches to structurally determined Pd-III/IV complexes starting from their Pd-II precursors, and the advances in this research area from early 2010 to late 2019 will be highlighted. Chemical oxidations exploiting various oxidizing agents including 1) hypervalent iodine reagents; 2) halogens; 3) electrophilic fluorination reagents; 4) alkyl/aryl halides; 5) ferrocenium salts; 6) peroxides/O-2; 7) sulfonyl chlorides; and 8) others are covered. A "greener" electrooxidation manner has also been reviewed.
引用
收藏
页码:9430 / 9444
页数:15
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