Bismuth Redox Catalysis: An Emerging Main-Group Platform for Organic Synthesis

被引:137
作者
Moon, Hye Won [1 ]
Cornella, Josep [1 ]
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
Main group catalysis; redox cycling; organobismuth; organic synthesis; heavy elements; PENTAVALENT ORGANOBISMUTH REAGENTS; LIGAND COUPLING REACTIONS; LIVING RADICAL POLYMERIZATION; COPPER-MEDIATED FLUORINATION; OXIDATIVE ADDITION; C-F; GROUP ELEMENTS; REDUCTIVE ELIMINATION; PREPARATIVE METHOD; OXYARYL DIANION;
D O I
10.1021/acscatal.1c04897
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bismuth has recently been shown to be able to maneuver between different oxidation states, enabling access to unique redox cycles that can be harnessed in the context of organic synthesis. Indeed, various catalytic Bi redox platforms have been discovered and revealed emerging opportunities in the field of main group redox catalysis. The goal of this perspective is to provide an overview of the synthetic methodologies that have been developed to date, which capitalize on the Bi redox cycling. Recent catalytic methods via low-valent Bi(II)/Bi(III), Bi(I)/Bi(III), and high-valent Bi(III)/Bi(V) redox couples are covered as well as their underlying mechanisms and key intermediates. In addition, we illustrate different design strategies stabilizing low-valent and high-valent bismuth species, and highlight the characteristic reactivity of bismuth complexes, compared to the lighter p-block and d-block elements. Although it is not redox catalysis in nature, we also discuss a recent example of non-Lewis acid, redox-neutral Bi(III) catalysis proceeding through catalytic organometallic steps. We close by discussing opportunities and future directions in this emerging field of catalysis. We hope that this Perspective will provide synthetic chemists with guiding principles for the future development of catalytic transformations employing bismuth.
引用
收藏
页码:1382 / 1393
页数:12
相关论文
共 177 条
[1]   Recent developments in the chemistry of non-trigonal pnictogen pincer compounds: from bonding to catalysis [J].
Abbenseth, Josh ;
Goicoechea, Jose M. .
CHEMICAL SCIENCE, 2020, 11 (36) :9728-9740
[2]   Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center [J].
Abdalla, Joseph A. B. ;
Riddlestone, Ian M. ;
Tirfoin, Remi ;
Aldridge, Simon .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (17) :5098-5102
[3]   OXIDATION OF ALPHA-HYDROXYKETONES WITH TRIPHENYLANTIMONY DIBROMIDE AND ITS CATALYTIC CYCLE [J].
AKIBA, K ;
OHNARI, H ;
OHKATA, K .
CHEMISTRY LETTERS, 1985, (10) :1577-1580
[4]   Aluminium-Mediated Carbon Dioxide Reduction by an Isolated Monoalumoxane Anion [J].
Anker, Mathew D. ;
Coles, Martyn P. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (50) :18261-18265
[5]  
[Anonymous], 1999, J AM CHEM SOC, V121, P3357
[6]  
[Anonymous], 2000, INT, V39, P2771
[7]  
[Anonymous], 1999, J AM CHEM SOC, V121, P3357
[8]  
[Anonymous], 2011, J AM CHEM SOC J AM CHEM SOC, V133, P5244
[9]  
Arduengo AJ, 1999, HELV CHIM ACTA, V82, P2348, DOI 10.1002/(SICI)1522-2675(19991215)82:12<2348::AID-HLCA2348>3.0.CO
[10]  
2-M