Metal–Ligand Cooperation by Aromatization–Dearomatization: A New Paradigm in Bond Activation and “Green” Catalysis
Top Cited Papers
- 8 July 2011
- journal article
- review article
- Published by American Chemical Society (ACS) in Accounts of Chemical Research
- Vol. 44 (8), 588-602
- https://doi.org/10.1021/ar2000265
Abstract
In view of global concerns regarding the environment and sustainable energy resources, there is a strong need for the discovery of new, green catalytic reactions. For this purpose, fresh approaches to catalytic design are desirable. In recent years, complexes based on “cooperating” ligands have exhibited remarkable catalytic activity. These ligands cooperate with the metal center by undergoing reversible structural changes in the processes of substrate activation and product formation. We have discovered a new mode of metal–ligand cooperation, involving aromatization–dearomatization of ligands. Pincer-type ligands based on pyridine or acridine exhibit such cooperation, leading to unusual bond activation processes and to novel, environmentally benign catalysis. Bond activation takes place with no formal change in the metal oxidation state, and so far the activation of H–H, C–H (sp2 and sp3), O–H, and N–H bonds has been demonstrated. Using this approach, we have demonstrated a unique water splitting process, which involves consecutive thermal liberation of H2 and light-induced liberation of O2, using no sacrificial reagents, promoted by a pyridine-based pincer ruthenium complex. An acridine pincer complex displays unique “long-range” metal–ligand cooperation in the activation of H2 and in reaction with ammonia. In this Account, we begin by providing an overview of the metal–ligand cooperation based on aromatization–dearomatization processes. We then describe a range of novel catalytic reactions that we developed guided by these new modes of metal–ligand cooperation. These reactions include the following: (1) acceptorless dehydrogenation of secondary alcohols to ketones, (2) acceptorless dehydrogenative coupling of alcohols to esters, (3) acylation of secondary alcohols by esters with dihydrogen liberation, (4) direct coupling of alcohols and amines to form amides and polyamides with liberation of dihydrogen, (5) coupling of esters and amines to form amides with H2 liberation, (6) selective synthesis of imines from alcohols and amines, (6) facile catalytic hydrogenolysis of esters to alcohols, (7) hydrogenolysis of amides to alcohols and amines, (8) hydrogenation of ketones to secondary alcohols under mild hydrogen pressures, (9) direct conversion of alcohols to acetals and dihydrogen, and (10) selective synthesis of primary amines directly from alcohols and ammonia. These reactions are efficient, proceed under neutral conditions, and produce no waste, the only byproduct being molecular hydrogen and/or water, providing a foundation for new, highly atom economical, green synthetic processes.This publication has 63 references indexed in Scilit:
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