Mechanistic Insights into Ruthenium-Catalyzed Production of H2 and CO2 from Methanol and Water: A DFT Study

被引:88
作者
Yang, Xinzheng [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, State Key Lab Struct Chem Unstable & Stable Speci, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
来源
ACS CATALYSIS | 2014年 / 4卷 / 04期
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
catalytic mechanism; dehydrogenation; methanol; water; carbon dioxide; ruthenium; MOLECULAR-ORBITAL METHODS; HYDROGEN-PRODUCTION; BASIS-SETS; DEHYDROGENATION; MIXTURES; COMPLEX; ECONOMY; BIOMASS;
D O I
10.1021/cs500061u
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A density functional theory study of the reaction mechanism of the production of H-2 and CO2 from methanol and water catalyzed by an aliphatic PNP pincer ruthenium complex, (PNP)Ru(H)CO, reveals three interrelated catalytic cycles for the release of three H-2 molecules: the dehydrogenation of methanol to formaldehyde, the coupling of formaldehyde and hydroxide for the formation of formic acid, and the dehydrogenation of formic acid. The formation of all three H-2 molecules undergoes the same self-promoted mechanism that features a methanol or a water molecule acting as a bridge for the transfer of a ligand proton to the metal hydride in a key intermediate, trans-(HPNP)Ru(H)(2)CO.
引用
收藏
页码:1129 / 1133
页数:5
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