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
相关论文
共 23 条
[1]   Selective Hydrogen Production from Methanol with a Defined Iron Pincer Catalyst under Mild Conditions [J].
Alberico, Elisabetta ;
Sponholz, Peter ;
Cordes, Christoph ;
Nielsen, Martin ;
Drexler, Hans-Joachim ;
Baumann, Wolfgang ;
Junge, Henrik ;
Beller, Matthias .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (52) :14162-14166
[2]  
Bullock R. M., 2010, Catalysis without Precious Metals
[3]   Hydrogen from catalytic reforming of biomass-derived hydrocarbons in liquid water [J].
Cortright, RD ;
Davda, RR ;
Dumesic, JA .
NATURE, 2002, 418 (6901) :964-967
[4]   Dihydrogen bonding: Structures, energetics, and dynamics [J].
Custelcean, R ;
Jackson, JE .
CHEMICAL REVIEWS, 2001, 101 (07) :1963-1980
[5]  
Frisch M, 2015, Gaussian 09, revision a 02
[6]   Hydrogen Evolution from Water/Alcohol Mixtures: Effective In Situ Generation of an Active Au/TiO2 catalyst [J].
Gaertner, Felix ;
Losse, Sebastian ;
Boddien, Albert ;
Pohl, Marga-Martina ;
Denurra, Stefania ;
Junge, Henrik ;
Beller, Matthias .
CHEMSUSCHEM, 2012, 5 (03) :530-533
[7]   INFLUENCE OF POLARIZATION FUNCTIONS ON MOLECULAR-ORBITAL HYDROGENATION ENERGIES [J].
HARIHARA.PC ;
POPLE, JA .
THEORETICA CHIMICA ACTA, 1973, 28 (03) :213-222
[8]   SELF-CONSISTENT MOLECULAR-ORBITAL METHODS .12. FURTHER EXTENSIONS OF GAUSSIAN-TYPE BASIS SETS FOR USE IN MOLECULAR-ORBITAL STUDIES OF ORGANIC-MOLECULES [J].
HEHRE, WJ ;
DITCHFIELD, R ;
POPLE, JA .
JOURNAL OF CHEMICAL PHYSICS, 1972, 56 (05) :2257-+
[9]   Hydrogen generation from formic acid and alcohols using homogeneous catalysts [J].
Johnson, Tarn C. ;
Morris, David J. ;
Wills, Martin .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (01) :81-88
[10]   SELF-CONSISTENT MOLECULAR-ORBITAL METHODS .20. BASIS SET FOR CORRELATED WAVE-FUNCTIONS [J].
KRISHNAN, R ;
BINKLEY, JS ;
SEEGER, R ;
POPLE, JA .
JOURNAL OF CHEMICAL PHYSICS, 1980, 72 (01) :650-654