A thermally robust ruthenium phosphonium alkylidene catalyst - the effect of more bulky N-heterocyclic carbene ligands on catalyst performance in olefin metathesis reactions

被引:10
作者
Leitao, Erin M. [1 ]
Piers, Warren E. [1 ]
Parvez, Masood [1 ]
机构
[1] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
来源
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 2013年 / 91卷 / 10期
基金
加拿大自然科学与工程研究理事会;
关键词
olefin metathesis; ruthenium; catalysis; ligand design; decomposition; RING-OPENING/CROSS-METATHESIS; CROSS-METATHESIS; GRUBBS CATALYSTS; NEW-GENERATION; COMPLEXES; EFFICIENT; POLYMERIZATION; BEARING; BENZYLIDENE; SELECTIVITY;
D O I
10.1139/cjc-2013-0156
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three new ruthenium phosphonium alkylidene complexes incorporating N-heterocyclic carbene ligands with bulky N-aryl groups (2,6-diethyl, L = 1,3-bis(2,6-diethylphenyl) imidazolin-2-ylidene (H2IDEP) and 2,6-diisopropyl, L = 1,3-bis(2, 6-diisopropylphenyl) imidazolin-2-ylidene (H2ID-i-PP)) were synthesized and characterized. The H2ID-i-PP supported complex was found to exhibit excellent thermal stabilities relative to the parent N-mesityl (N-Mes) complexes as well as the H2IDEP supported complexes. All three phosphonium alkylidenes were evaluated in comparison to the N-Mes derivative and Grubbs second generation catalyst using standard olefin metathesis reactions and conditions. The complex containing the bulky H2ID-i-PP ligand was found to have excellent activity and longevity in comparison to the other catalysts. Although initiation rates were slow for this sterically bulky precatalyst, its superior activity led to the best overall efficiency in test reactions.
引用
收藏
页码:935 / 942
页数:8
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