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Efficient hydrogenation of organic carbonates, carbamates and formates indicates alternative routes to methanol based on CO2 and CO

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TLDR
Producing methanol — useful as both a fuel and a synthetic building block — from carbon monoxide and carbon dioxide has been achieved using homogeneous catalytic hydrogenation of carbonates, carbamates and formates.
Abstract
Catalytic hydrogenation of organic carbonates, carbamates and formates is of significant interest both conceptually and practically, because these compounds can be produced from CO2 and CO, and their mild hydrogenation can provide alternative, mild approaches to the indirect hydrogenation of CO2 and CO to methanol, an important fuel and synthetic building block. Here, we report for the first time catalytic hydrogenation of organic carbonates to alcohols, and carbamates to alcohols and amines. Unprecedented homogeneously catalysed hydrogenation of organic formates to methanol has also been accomplished. The reactions are efficiently catalysed by dearomatized PNN Ru(II) pincer complexes derived from pyridine- and bipyridine-based tridentate ligands. These atom-economical reactions proceed under neutral, homogeneous conditions, at mild temperatures and under mild hydrogen pressures, and can operate in the absence of solvent with no generation of waste, representing the ultimate 'green' reactions. A possible mechanism involves metal-ligand cooperation by aromatization-dearomatization of the heteroaromatic pincer core.

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Citations
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Journal ArticleDOI

Theoretical insights into CO2 hydrogenation to methanol by a Mn–PNP complex

TL;DR: In this paper, the authors investigated the catalytic activity of PNP-based Mn(I), Fe(II), and Ru(II) homogeneous complexes for CO2 hydrogenation to methanol.
Journal ArticleDOI

Pushing Back the Limits of Hydrosilylation: Unprecedented Catalytic Reduction of Organic Ureas to Formamidines

TL;DR: In this paper, the C=O group in urea derivatives is the least electrophilic function within the series of carbonyl groups in aldehydes, ketones, esters, amides, carbonates, carbamates and ureas.
Journal ArticleDOI

Multifunctional and Sustainable Fe-Iminopyridine Complexes for the Synthesis of Cyclic Carbonates.

TL;DR: The optimal catalyst possesses a halide counteranion and a hydrogen bond donor to activate the epoxide for ring opening, affording a single-component, cocatalyst-free catalytic system.
Journal ArticleDOI

Effects of Metal Coordination on the π-System of the 2,5-Bis-{(pyrrolidino)-methyl}-pyrrole Pincer Ligand

TL;DR: The changes in the aromaticity of the pyrrole ring upon coordination have been rationalized according to the interaction of the π-system with the metal.
Journal ArticleDOI

A metathesis model for the dehydrogenative coupling of amines with alcohols and esters into carboxamides by Milstein's [Ru(PNN)(CO)(H)] catalysts.

TL;DR: Alternative, more direct OR/H and NHR/H metal/acyl metathesis routes to coupling that circumvent the intermediacy of the hemiacetal and the hemiaminal are investigated.
References
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Journal ArticleDOI

Mechanisms of the H2-hydrogenation and transfer hydrogenation of polar bonds catalyzed by ruthenium hydride complexes

TL;DR: In this article, the authors classified the catalytic cycles for the H2-hydrogenation (H) and transfer hydrogenation (T) of CO and cN bonds catalyzed by over 100 ruthenium hydride complexes in organic and aqueous media.
Journal ArticleDOI

Direct Synthesis of Amides from Alcohols and Amines with Liberation of H2

TL;DR: A reaction in which primary amines are directly acylated by equimolar amounts of alcohols to produce amides and molecular hydrogen in high yields and high turnover numbers is reported.
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