Bond Activation by Metal-Ligand Cooperation: Design of "Green" Catalytic Reactions Based on Aromatization-Dearomatization of Pincer Complexes

被引:120
作者
Gunanathan, Chidambaram [1 ]
Milstein, David [1 ]
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
来源
BIFUNCTIONAL MOLECULAR CATALYSIS | 2011年 / 37卷
基金
欧洲研究理事会; 以色列科学基金会;
关键词
Alcohols; Amides; Amines; Carbon dioxide; Catalysis; Dehydrogenative coupling; Esters; Hydrogen; Imines; Iridium; Metal-ligand cooperation; O-H activation; Pincer complexes; PNN; PNP; Ruthenium; FE-ONLY HYDROGENASE; C-H ACTIVATION; SUPERCRITICAL CARBON-DIOXIDE; PNP-TYPE COMPLEXES; ELECTRON-RICH; AMIDE SYNTHESIS; FORMIC-ACID; RUTHENIUM COMPLEXES; ALCOHOL DEHYDROGENATION; HOMOGENEOUS CATALYSIS;
D O I
10.1007/3418_2011_6
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We have developed a new mode of bifunctional catalysis based on metal-ligand cooperation, involving aromatization-dearomatization of pyridine-and acridine-derived pincer complexes. This type of metal-ligand cooperation is involved in the recently discovered environmentally benign reactions of alcohols, catalyzed by PNP and PNN pincer complexes of ruthenium, including: (a) dehydrogenation of secondary alcohols to ketones, (b) dehydrogenative coupling of primary alcohols to form esters and H-2, (c) unprecedented amide synthesis: catalytic coupling of amines with alcohols, with liberation of H-2, (d) direct synthesis of imines from alcohols and amines with H-2 liberation, (e) direct conversion of alcohols to acetals with H-2 liberation, (f) selective synthesis of primary amines from alcohols and ammonia, and (g) hydrogenation of esters to alcohols under mild conditions. These reactions are very efficient, proceed under neutral conditions, and produce no waste.
引用
收藏
页码:55 / 84
页数:30
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