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首页> 外文期刊>Organometallics >Synthesis, Structure, and Reactivity of Cationic Ruthenium(II) Carbene Complexes with Bulky Chelating Bisphosphines: Design of Highly Active Ring Opening Metathesis Polymerization (ROMP) Catalysts
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Synthesis, Structure, and Reactivity of Cationic Ruthenium(II) Carbene Complexes with Bulky Chelating Bisphosphines: Design of Highly Active Ring Opening Metathesis Polymerization (ROMP) Catalysts

机译:带有大体积螯合双膦的阳离子钌(II)卡宾配合物的合成,结构和反应性:高活性开环易位聚合(ROMP)催化剂的设计

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摘要

Complexes of the type [{t-Bu)_2P(CH_2_nP(t-Bu)_2-kappa~2P}XRu=CHR]_2(Y)_2 have been prepared and characterized in solution as well as in the solid state. Parameters governing the ring opening metathesis polymerization (ROMP) activity of these highly active ruthenium catalysts in solution have been assessed. Especially, chloro-bridged dinuclear dicationic ruthenium carbenes with a bis(di-tert-butylphosphino)methane ligand and weakly coordinating or noncoordinating anions display extremely high ROMP activity. Comparison of the solution-phase reactivity reported here with high throughput screening results from gas-phase experiments provide further mechanistic insight into the metathesis reaction with these compounds.
机译:已经制备了[{t-Bu)_2P(CH_2_nP(t-Bu)_2-kappa〜2P} XRu = CHR] _2(Y)_2类型的配合物,并在溶液和固态中对其进行了表征。评估了这些高活性钌催化剂在溶液中的开环复分解聚合(ROMP)活性,特别是具有双(二叔丁基膦基)甲烷配体和弱配位或非配位阴离子的氯桥联二核基钌钌。 ROMP活性高。本文报道的溶液相反应性与气相实验的高通量筛选结果进行了比较,从而进一步了解了这些化合物的复分解反应的机理。

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