Homogeneous conversion of methane to methanol.: 1.: Catalytic activation and functionalization of methane by cis-platin in sulfuric acid:: A density functional study of the thermochemistry

被引:49
作者
Mylvaganam, K
Bacskay, GB
Hush, NS [1 ]
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Univ Sydney, Dept Biochem, Sydney, NSW 2006, Australia
关键词
D O I
10.1021/ja983753i
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The recent announcement by Periana et al. (Science 1998, 280, 560) of 70% one-pass homogeneous catalysis of methane-to-methanol :conversion with high selectivity in sulfuric acid solution under moderate conditions represents an important advance in the selective oxidation of alkanes, an-area of considerable current interest and activity. The conversion is catalyzed by bis(2,2' bipyrimidine)Pt(II)Cli. In this work, the thermodynamics of the activation and functionalization steps of the related cis-platin-catalyzed process in H2SO4 are calculated using density functional techniques, including the calculation of solvation free energies by a dielectric continuum method. It is concluded that electrophilic attack by CH4 on an intermediate which may:be regarded as a tetracoordinate solvated analogue of a gas-phase, T-shaped, three-coordinate Pt(LI) species, followed by oxidation of the resulting methyl complex to a methyl bisulfate eater, is thermodynamically feasible. This is in general accord with the mechanism proposed by Periana et al., but now, on the basis of the computational predictions, the nature of the active catalyst, as well as that of the intermediates, can be more precisely defined. While the alternative mechanism of oxidative addition does not appear to be thermodynamically feasible when using Pt(II) catalysts, catalysis by a Pt(IV) species is predicted to be, on thermodynamic grounds, a viable alternative pathway.
引用
收藏
页码:4633 / 4639
页数:7
相关论文
共 27 条
[1]  
[Anonymous], 1990, Selective Hydrocarbon Activation
[2]   SELECTIVE INTERMOLECULAR CARBON-HYDROGEN BOND ACTIVATION BY SYNTHETIC METAL-COMPLEXES IN HOMOGENEOUS SOLUTION [J].
ARNDTSEN, BA ;
BERGMAN, RG ;
MOBLEY, TA ;
PETERSON, TH .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (03) :154-162
[3]   A new definition of cavities for the computation of solvation free energies by the polarizable continuum model [J].
Barone, V ;
Cossi, M ;
Tomasi, J .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (08) :3210-3221
[4]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[5]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[6]   The mechanism of a C-H bond activation reaction in room-temperature alkane solution [J].
Bromberg, SE ;
Yang, H ;
Asplund, MC ;
Lian, T ;
McNamara, BK ;
Kotz, KT ;
Yeston, JS ;
Wilkens, M ;
Frei, H ;
Bergman, RG ;
Harris, CB .
SCIENCE, 1997, 278 (5336) :260-263
[7]   Ligand exchange reactions in molecular hydrogen complexes of Osmium(II): A quantum chemical study using density functional theory [J].
Bytheway, I ;
Bacskay, GB ;
Hush, NS .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (36) :14899-14903
[8]   Quantum chemical study of the properties of molecular hydrogen complexes of osmium(II): A comparison of density functional and conventional ab initio methods [J].
Bytheway, I ;
Bacskay, GB ;
Hush, NS .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (15) :6023-6031
[9]   Solvent effects .5. Influence of cavity shape, truncation of electrostatics, and electron correlation ab initio reaction field calculations [J].
Foresman, JB ;
Keith, TA ;
Wiberg, KB ;
Snoonian, J ;
Frisch, MJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (40) :16098-16104
[10]  
Frisch M.J., 1995, GAUSSIAN 94 REVISION