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Elucidating the Key Role of Phosphine-Sulfonate Ligands in Palladium-Catalyzed Ethylene Polymerization: Effect of Ligand Structure on the Molecular Weight and Linearity of Polyethylene

机译:阐明膦磺酸盐配体在钯催化的乙烯聚合中的关键作用:配体结构对聚乙烯分子量和线性的影响

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The mechanism of linear polyethylene formation catalyzed by palladium/phosphine sulfonate and the effect of the ligand structure on the catalytic performance, such as linearity and molecular weight of the polyethylene, were reinvestigated theoretically and experimentally. We used dispersion-corrected density functional theory (DFT-D3) to study the entire mechanism of polyethylene formation from (R2PC6H4SO3)PdMe(2,6-lutidine) (R = Me, t-Bu) and elucidated the key steps that determine the molecular weight and linearity of the polyethylene. The alkylpalladium ethylene complex is the key intermediate for both linear propagation and fi-hydride elimination from the growing polymer chain. On the basis of the key species, the effects of substituents on the phosphorus atom (R = t-Bu, i-Pr, Cy, Men, Ph, 2-MeOC6H4, biAr) were further investigated theoretically to explain the experimental results in a comprehensive manner. Thus, the experimental trend of molecular weights of polyethylene could be correlated to the AA G* value between (i) the transition state of linear propagation and (ii) the transition state of the path for ethylene dissociation leading to fi-hydride elimination. Moreover, the experimental behavior of the catalysts under varied ethylene pressure was well explained by our computation on the small set of key species elucidated from the entire mechanism. In our additional experimental investigations, [o-Ani(2)PC(6)H(4)SO(3)]PdH[P(t-Bu)(3)] catalyzed a hydrogen/ deuterium exchange reaction between ethylene and Me0D. The deuterium incorporation from Me0D into the main chain of polyethylene, therefore, can be explained by the incorporation of deuterated ethylene formed by a small amount of Pd H species. These insights into the palladium/phosphine sulfonate system provide a comprehensive understanding of how the phosphine sulfonate ligands function to produce linear polyethylene.
机译:从理论上和实验上对钯/膦磺酸盐催化的线性聚乙烯形成机理以及配体结构对聚乙烯的线性和分子量等催化性能的影响进行了研究。我们使用分散校正的密度泛函理论(DFT-D3)研究了由(R2PC6H4SO3)PdMe(2,6-lutidine)(R = Me,t-Bu)形成聚乙烯的整个机理,并阐明了确定聚乙烯的分子量和线性。烷基钯乙烯络合物是线性链增长和从增长的聚合物链中消除氢氟酸的关键中间体。在关键物种的基础上,进一步研究了取代基对磷原子(R = t-Bu,i-Pr,Cy,Men,Ph,2-MeOC6H4,biAr)的影响,以解释在全面的方式。因此,聚乙烯分子量的实验趋势可以与(i)线性传播的过渡态和(ii)导致解离氢化物的乙烯解离的路径的过渡态之间的AA G *值相关。此外,通过我们对整个机理阐明的少量关键物种的计算,可以很好地解释催化剂在乙烯压力变化下的实验行为。在我们的其他实验研究中,[o-Ani(2)PC(6)H(4)SO(3)] PdH [P(t-Bu)(3)]催化了乙烯与MeOD之间的氢/氘交换反应。因此,从Me0D到聚乙烯主链中的氘掺入可以通过少量Pd H物种形成的氘代乙烯的掺入来解释。这些对钯/膦磺酸盐体系的见解提供了对膦磺酸盐配体如何产生线性聚乙烯的全面了解。

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