High turnover numbers with ruthenium-based metathesis catalysts

被引:1
|
作者
Dinger, MB [1 ]
Mol, JC [1 ]
机构
[1] Univ Amsterdam, Fac Sci, Inst Mol Chem, NL-1018 WV Amsterdam, Netherlands
关键词
catalytic activity; N-heterocyclic carbene (NHC) ligands; metathesis; P ligands; ruthenium;
D O I
10.1002/1615-4169(200208)344:6/7<671::AID-ADSC671>3.0.CO;2-G
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Effective turnover numbers (TON's) and turnover frequencies (TOF's) of unprecedented magnitude have been obtained for the metathesis of various substrates in the presence of ruthenium-based catalysts, without the use of an additional solvent. For the self-metathesis of 1-octene, the 2nd generation Grubbs' catalyst (IMesH(2))(PCy3)(Cl)(2)Ru=CHPh (2a) (IMesH(2) = 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene) gave TON's 5 times higher than those of the 1st generation catalyst (PCy3)(2)(Cl)(2)Ru=CHPh (1) while maintaining a high degree of selectivity for the formation of the product 7-tetradecene. Moreover, the catalyst (IPrH2)(PCy3)(Cl)(2)Ru=CHPh (2b), bearing the extremely bulky 1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazol-2-ylidene ligand (IPrH2), gave TON's 6 times higher (TON > 640,000) and initial TOF's 20 times higher than those of 2a at ambient temperature. At elevated temperatures, TOF's were twice as high and initial TOF's were 6 times as high for 2b relative to 2a, and with nearly 100% selectivity. Initial TOF's exceeding 3,800 s(-1) could be achieved with 2b at 60degreesC. Under similar conditions, comparable TON's for the self-metathesis of trans-4-decene and triethyl oleate, and the ring-closing metathesis of diethyl diallylmalonate were also obtained.
引用
收藏
页码:671 / 677
页数:7
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