化学
催化作用
环氧化物
烯烃纤维
药物化学
乙烯
配体(生物化学)
戒指(化学)
催化循环
过氧化氢
光化学
分解
立体化学
有机化学
受体
生物化学
作者
Luı́s F. Veiros,A. Prazeres,Paulo J. Costa,Carlos C. Romão,Fritz E. Kühn,Maria José Calhorda
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2006-01-01
卷期号: (11): 1383-1383
被引量:99
摘要
DFT calculations suggest that the catalytic epoxidation of olefins by Mo(vi) complexes, modeled by MoO2Br2(MeN=C(H)-C(H)=NMe), in the presence of MeOOH, the model for tert-butyl hydroperoxide, starts with a hydrogen transfer from the peroxide to one of the terminal Mo=O oxygen atoms and the remaining MeOO anion binds as a seventh ligand, forming a five-membered Mo-O(alpha)-O(beta)(Me)...H-O-Mo ring held together by a hydrogen bond. In the second step, a concerted approach of ethylene to the Mo-O(alpha) bond gives rise to an intermediate containing a seven-membered Mo-C-C-O(alpha)-O(beta)(Me)...H-O-Mo ring. In the final step, decomposition of the intermediate leads to the starting complex, alcohol and the epoxide. The activation energy for the addition of the olefin (second step) is the highest one, in agreement with available kinetic studies showing that the catalyst formation is not always a rate-limiting step. DFT calculations also show that the alcohol by-product (MeOH) can react with the starting complex, competing with ROOH and hence leading to the progressive catalyst poisoning, which has been observed experimentally.
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