Janse van Rensburg Werner, Steynberg Petrus J, Meyer Wolfgang H, Kirk Megan M, Forman Grant S
Sasol Technology (Pty), Ltd., R&D Division, 1 Klasie Havenga Road, Sasolburg 9570, South Africa.
J Am Chem Soc. 2004 Nov 10;126(44):14332-3. doi: 10.1021/ja0453174.
Ruthenacyclobutane decomposition, involving competitive beta-hydride transfer to Ru and reductive olefin elimination during ruthenium-catalyzed olefin metathesis, is predicted by density functional theory calculations and experimentally confirmed by propene and butene formation during degenerate Ru-methylidene-catalyzed metathesis of ethylene. The results provide new focus on the nature of ruthenium metathesis catalyst decomposition under catalytic conditions.
通过密度泛函理论计算预测,在钌催化的烯烃复分解反应中,钌环丁烷分解涉及竞争性的β-氢化物向钌的转移以及还原烯烃消除反应,并且在乙烯的简并亚甲基钌催化复分解反应过程中生成丙烯和丁烯的实验结果证实了这一点。这些结果为催化条件下钌复分解催化剂分解的本质提供了新的关注点。