Lenz Tim M, Chiorescu Ion, Napoli Fabrizio E, Liu Jin Y, Rieger Bernhard
Wacker-Lehrstuhl für Makromolekulare Chemie Catalysis Research Center, Technische Universität München TUM School of Natural Sciences, Lichtenbergstraße 4, 85748, Garching Garching bei München, Germany.
Department Chemie, Technische Universität München TUM School of Natural Sciences, Lichtenbergstraße 4, 85748, Garching Garching bei München, Germany.
Angew Chem Int Ed Engl. 2024 Sep 16;63(38):e202406848. doi: 10.1002/anie.202406848. Epub 2024 Aug 20.
The synthesis of group IV metallocene precatalysts for the polymerization of propylene generally yields two different isomers: The racemic isomer that produces isotactic polypropylene (iPP) and the meso isomer that produces atactic polypropylene (aPP). Due to its poor physical properties, aPP has very limited applications. To avoid obtaining blends of both polymers and thus diminish the mechanical and thermal properties of iPP, the meso metallocene complexes need to be separated from the racemic ones tediously-rendering the metallocene-based polymerization of propylene industrially far less attractive than the Ziegler/Natta process. To overcome this issue, we established an isomerization protocol to convert meso metallocene complexes into their racemic counterparts. This protocol increased the yield of iPP by 400 % while maintaining the polymer's excellent physical properties and was applicable to both hafnocene and zirconocene complexes, as well as different precatalyst activation methods. Through targeted variation of the ligand frameworks, methoxy groups at the indenyl moieties were found to be the structural motifs responsible for an isomerization to take place-this experimental evidence was confirmed by density functional theory calculations. Liquid injection field desorption ionization mass spectrometry, as well as H and Si nuclear magnetic resonance studies, allowed the proposal of an isomerization mechanism.
用于丙烯聚合的第IV族茂金属预催化剂的合成通常会产生两种不同的异构体:产生全同立构聚丙烯(iPP)的外消旋异构体和产生无规立构聚丙烯(aPP)的内消旋异构体。由于其物理性能较差,aPP的应用非常有限。为了避免获得两种聚合物的共混物从而降低iPP的机械和热性能,需要繁琐地将内消旋茂金属配合物与外消旋配合物分离,这使得基于茂金属的丙烯聚合在工业上远不如齐格勒/纳塔工艺有吸引力。为了克服这个问题,我们建立了一种异构化方案,将内消旋茂金属配合物转化为它们的外消旋对应物。该方案使iPP的产率提高了400%,同时保持了聚合物优异的物理性能,并且适用于二茂铪和二茂锆配合物以及不同的预催化剂活化方法。通过有针对性地改变配体骨架,发现茚基部分的甲氧基是导致异构化发生的结构单元——这一实验证据得到了密度泛函理论计算的证实。液体注入场解吸电离质谱以及氢和硅核磁共振研究,使得我们能够提出一种异构化机理。