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Journal ArticleDOI

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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Journal ArticleDOI

Hydrogenation of CO2 into formic acid using a palladium catalyst on chitin

TL;DR: In this paper, a palladium catalyst on chitin was used to accelerate the hydrogenation of CO2 in a C-1 source of carbon dioxide into chemicals using a simple wet-impregnation method and then characterized by FT-IR, ICP, XRD, FESEM, TEM and XPS.
Journal ArticleDOI

Are Amines the Holy Grail for Facilitating CO2 Reduction

TL;DR: A variety of catalytic methods for the CO2 reduction reaction (CO2 RR) have been developed, including hydrogenations and electrochemical or photochemical reductions as mentioned in this paper, and some of these recent findings are discussed in a broader context in an attempt to provide guidelines for the design of new catalysts with enhanced activity and selectivity.
Journal ArticleDOI

Structurally Versatile Ligand System for the Ruthenium Catalyzed One-Pot Hydrogenation of CO2 to Methanol

TL;DR: In this paper, the direct hydrogenation of carbon dioxide to methanol represents a challenging transformation for molecular catalyst, and only a few systems facilitate this reaction, where molecular complexes are used.
Journal ArticleDOI

Ammonia borane confined by nitrogen-containing carbon nanotubes: enhanced dehydrogenation properties originating from synergetic catalysis and nanoconfinement

TL;DR: In this article, an ammonia borane (AB)@polypyrrole (PPy) combined system was presented, which combines synergetic catalysis of nitrogen atoms with nanoconfinement in nanotubes, resulting in a significant improvement in the dehydrogenation properties.
Journal ArticleDOI

Revised Mechanisms of the Catalytic Alcohol Dehydrogenation and Ester Reduction with the Milstein PNN Complex of Ruthenium

TL;DR: The combined experimental/DFT computational study of RuH2(CO) suggests that this dihydride is the catalyst of the acceptorless alcohol dehydrogenation and ester hydrogenatio....
References
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Journal ArticleDOI

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

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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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