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Living polymerization of phenylacetylene with tetrafluorobenzobarrelene ligand-containing rhodium catalyst systems featuring the synthesis of high molecular weight polymer

机译:苯乙炔与含四氟苯并barrelene配体的铑催化剂体系的活性聚合,具有高分子量聚合物的合成

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Highly active Rh-based living polymerization catalysts were developed, which enabled the synthesis of poly( phenylacetylene) with high molecular weight and narrow molecular weight distributions (e.g., Mn) 195000, M-w/M-n = 1.06). For instance, a Rh-based ternary catalyst system composed of [(tfb)RhCl](2) (1) (tfb, tetrafluorobenzobarrelene), Ph2C=C(Ph)Li, and Ph3P (1:5:10) mediated the living polymerization of phenylacetylene (PA) with virtually 100% initiation efficiency. Furthermore, a well-defined vinylrhodium complex [(tfb)Rh-{-C(Ph=CPh2}(Ph3P)] (2) also polymerized PA in a living fashion with quantitative initiation efficiency in the presence of at least 5 equiv of Ph3P to Rh. The livingness of these polymerizations was confirmed by multistage polymerization, first-order linear plot, and effect of initial monomer concentration on molecular weight and MWD, and their initiation efficiencies were practically quantitative. A salient feature of catalyst 2 is its high activity even at a very low concentration ([M](0)/[Rh] = 4000, [Rh] = 0.125 mM) to quantitatively afford a high molecular weight polymer (Mn = 401000) having very narrow MWD (M-w/M-n = 1.12). The formed polymers possessed highly stereoregular cis-transoidal main chain (cis contents >= 99%).
机译:开发了高活性的Rh基活性聚合催化​​剂,该催化剂能够合成具有高分子量和窄分子量分布(例如,Mn)为195000,M-w / M-n = 1.06的聚苯乙炔。例如,由[(tfb)RhCl](2)(1)(tfb,四氟苯并戊烯),Ph2C = C(Ph)Li和Ph3P(1:5:10)组成的Rh基三元催化剂体系介导了生物。苯乙炔(PA)的聚合反应,引发效率几乎为100%。此外,定义明确的乙烯基铑配合物[(tfb)Rh-{-C(Ph = CPh2}(Ph3P)](2)在至少5当量的Ph3P存在的情况下,还可以定量活化的活性形式聚合PA。通过多阶段聚合,一阶线性图和初始单体浓度对分子量和MWD的影响证实了这些聚合反应的活性,并且它们的引发效率实际上是定量的,催化剂2的显着特征是其高活性。即使在非常低的浓度下([M](0)/ [Rh] = 4000,[Rh] = 0.125 mM))也可以定量提供具有非常窄的MWD(Mw / Mn = 1.12)的高分子量聚合物(Mn = 401000) )。形成的聚合物具有高度立体规则的顺式-反式主链(顺式含量> = 99%)。

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