» Articles » PMID: 21778980

Efficient Hydrogenation of Organic Carbonates, Carbamates and Formates Indicates Alternative Routes to Methanol Based on CO2 and CO

Overview
Journal Nat Chem
Specialty Chemistry
Date 2011 Jul 23
PMID 21778980
Citations 39
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Autocatalytic Activation of a Ruthenium-PNN-Pincer Hydrogenation Catalyst.

Perez J, Kirlin F, Reynolds E, Altomare-Jarczyk C, Joseph B, Keith J ACS Catal. 2024; 14(21):16497-16507.

PMID: 39507487 PMC: 11536344. DOI: 10.1021/acscatal.4c04475.


Toward Methanol Production by CO Hydrogenation beyond Formic Acid Formation.

Onishi N, Himeda Y Acc Chem Res. 2024; 57(19):2816-2825.

PMID: 39284577 PMC: 11447816. DOI: 10.1021/acs.accounts.4c00411.


Highly Enantiomerically Enriched Secondary Alcohols via Epoxide Hydrogenolysis.

Borden O, Joseph B, Head M, Ammons O, Kim D, Bonino A Organometallics. 2024; 43(13):1490-1501.

PMID: 38993820 PMC: 11234370. DOI: 10.1021/acs.organomet.4c00214.


A mechanistic study on conversion of carbon dioxide into formic acid promoted by 1-ethyl-2, 3-dimethyl-imidazolium nitrite.

Bello T, Alvim R, Bresciani A, Nascimento C, Alves R J Mol Model. 2024; 30(7):231.

PMID: 38935147 DOI: 10.1007/s00894-024-06013-z.


Catalytic regeneration of metal-hydrides from their corresponding metal-alkoxides the hydroboration of carbonates to obtain methanol and diols.

Deka H, Ritacco I, Fridman N, Caporaso L, Eisen M Chem Sci. 2023; 14(31):8369-8379.

PMID: 37576386 PMC: 10413203. DOI: 10.1039/d3sc01700a.


References
1.
Ito M, Ikariya T . Catalytic hydrogenation of polar organic functionalities based on Ru-mediated heterolytic dihydrogen cleavage. Chem Commun (Camb). 2007; (48):5134-42. DOI: 10.1039/b709704b. View

2.
Schaffner B, Schaffner F, Verevkin S, Borner A . Organic carbonates as solvents in synthesis and catalysis. Chem Rev. 2010; 110(8):4554-81. DOI: 10.1021/cr900393d. View

3.
Nunez Magro A, Eastham G, Cole-Hamilton D . The synthesis of amines by the homogeneous hydrogenation of secondary and primary amides. Chem Commun (Camb). 2007; (30):3154-6. DOI: 10.1039/b706635j. View

4.
Federsel C, Jackstell R, Boddien A, Laurenczy G, Beller M . Ruthenium-catalyzed hydrogenation of bicarbonate in water. ChemSusChem. 2010; 3(9):1048-50. DOI: 10.1002/cssc.201000151. View

5.
O W, Lough A, Morris R . The hydrogenation of molecules with polar bonds catalyzed by a ruthenium(II) complex bearing a chelating N-heterocyclic carbene with a primary amine donor. Chem Commun (Camb). 2010; 46(43):8240-2. DOI: 10.1039/c0cc02664f. View