期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 14, 页码 3641-3644出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201309043
关键词
acetylene; alloys; heterogeneous catalysis; platinum; reaction mechanisms
资金
- National Science Foundation [CHE-1129417, CBET-1264453]
- Directorate For Engineering
- Div Of Chem, Bioeng, Env, & Transp Sys [1264453] Funding Source: National Science Foundation
Vibrational spectroscopic measurements and density functional calculations were used to identify a preferential catalytic mechanism for the transformation of acetylene, HCCH, to vinylidene, CCH2, on surfaces of Pt-Sn ordered alloys. In this mechanism, two adjacent Pt atoms adsorb an acetylene molecule and a third neighboring Pt atom is required for stabilizing the reacting H atom during the transformation. Therefore, unlike a direct H shift along the CC bond in organometallic compounds with a single transition-metal atom, this mechanism has a geometric site requirement of three adjacent Pt atoms in the form of a three-fold site. The same geometric site requirement is identified for preferential CH bond cleavage of acetylene with the formation of adsorbed CCH and H species. In the absence of three-fold Pt sites, the reaction mechanism changes, and reactions of H transfer and CH bond cleavage are suppressed.
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