A DFT Study of Tungsten-Methylidene Formation on a W/ZSM-5 Zeolite: The Metathesis Active Site

被引:29
|
作者
Maihom, Thana [1 ,2 ,3 ]
Probst, Michael [4 ]
Limtrakul, Jumras [5 ]
机构
[1] Kasetsart Univ, Fac Liberal Arts & Sci, Dept Chem, Nakhon Pathom 73140, Thailand
[2] Kasetsart Univ, Dept Chem, Bangkok 10900, Thailand
[3] Kasetsart Univ, NANOTEC Ctr Nanoscale Mat Design Green Nanotechno, Bangkok 10900, Thailand
[4] Univ Innsbruck, Inst Ion Phys & Appl Phys, A-6020 Innsbruck, Austria
[5] Vidyasirimedhi Inst Sci & Technol, Dept Mat Sci & Engn, Rayong 21210, Thailand
关键词
density functional calculations; metathesis; methylidene; tungsten oxide; zeolites; DENSITY-FUNCTIONAL THEORY; HETEROGENEOUS OLEFIN METATHESIS; RHENIUM OXIDE CATALYSTS; MOLYBDENA-ALUMINA; REACTION-MECHANISMS; NOBEL LECTURE; THEORETICAL INVESTIGATIONS; BENZENE ALKYLATION; FAUJASITE ZEOLITE; SILICA-ALUMINA;
D O I
10.1002/cphc.201500427
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
Tungsten-methylidene formation from ethene on either the W-IV, W-V, or W-VI active sites of a W/ZSM-5 zeolite is investigated by using the M06-L functional. The reaction is assumed to proceed in two steps; the first step is the [2+2] cycloaddition between ethene and the W-O active site to form an oxametallacycle intermediate. The intermediate is then decomposed to produce the W-methylidene active site from the metathesis reaction. The overall activation barrier of the reaction on W-VI (27.3kcalmol(-1)) is considerably lower than the ones for W-IV and W-V (69.4 and 37.1kcalmol(-1), respectively). Moreover, the reaction involving the W-VI site also stabilizes intermediates and products to a larger extent than the ones on the W-IV and W-V sites. As a result, we have demonstrated that the reaction of the W-methylidene metathesis active site is both kinetically and thermodynamically favored to occur on the W-VI active site of the zeolite.
引用
收藏
页码:3334 / 3339
页数:6
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