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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Ruthenium indenylidene complexes bearing N-alkyl/N-mesityl-substituted N-heterocyclic carbene ligands
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Ruthenium indenylidene complexes bearing N-alkyl/N-mesityl-substituted N-heterocyclic carbene ligands

机译:带有N-烷基/ N-间苯二甲酰基取代的N-杂环卡宾配体的茚基钌配合物

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摘要

We report on the synthesis and characterization of second generation ruthenium indenylidene catalysts bearing unsymmetrical N-heterocyclic carbene (NHC) ligands denoted as RuCl2(3-phenyl-1-indenylidene)(1-mesityl-3-R-4,5-dihydroimidazol-2-ylidene)(PCy3), in which R is methyl 8a, octyl 8b or cyclohexyl 8c. The characterization of 8a-c was performed by NMR spectroscopy, elemental analysis, IR, HRMS and single-crystal X-ray diffraction analysis. In addition, the catalytic activity of the obtained initiators was evaluated in various representative metathesis reactions. The results reveal that the complexes 8a-c, bearing an N-alkyl side on the NHC, show a faster catalytic initiation than the reference complex 2. Complex 8a, which performs the best among the investigated indenylidene complexes, exhibits slower initiation but better overall efficiency than its benzylidene analogue 1c, especially in a low catalyst loading.
机译:我们报告的合成和表征第二代钌茚并亚烷基催化剂带有不对称的N-杂环卡宾(NHC)配体表示为RuCl2(3-苯基-1-茚基)(1-甲磺酰基-3-R-4,5-二氢咪唑- 2-亚烷基)(PCy3),其中R为甲基8a,辛基8b或环己基8c。 8a-c的表征是通过NMR光谱,元素分析,IR,HRMS和单晶X射线衍射分析进行的。另外,在各种代表性的复分解反应中评估了所得引发剂的催化活性。结果表明,在NHC上带有N-烷基侧的配合物8a-c显示出比参考配合物2更快的催化引发。配合物8a在研究的茚二烯配合物中表现最佳,引发速度较慢,但​​总体上更好效率比其亚苄基类似物1c高,尤其是在催化剂用量较低的情况下。

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