Woof Callum R, Durand Derek J, Webster Ruth L
Department of Chemistry, University of Bath Claverton Down, Bath, BA2 7AY, UK.
School of Chemistry, University of Bristol Cantock's Close, Bristol, BS8 1TS, UK.
Chemistry. 2021 Aug 25;27(48):12335-12340. doi: 10.1002/chem.202101078. Epub 2021 Jul 16.
Herein, we report an iron(II)-catalyzed polymerization of arylallenes. This reaction proceeds rapidly at room temperature in the presence of a hydride co-catalyst to generate polymers of weight up to M =189 000 Da. We have determined the polymer structure and chain length for a range of monomers through a combination of NMR, differential scanning calorimetry (DSC) and gel permeation chromatography (GPC) analysis. Mechanistically, we postulate that the co-catalyst does not react to form an iron(II) hydride in situ, but instead the chain growth is proceeding via a reactive Fe(III) species. We have also performed kinetic and isotopic experiments to further our understanding. The formation of a highly unusual 1,3-substituted cyclobutane side-product is also investigated.
在此,我们报道了铁(II)催化的芳基丙二烯聚合反应。该反应在室温下,在氢化物共催化剂存在下迅速进行,生成重量高达M = 189 000 Da的聚合物。我们通过核磁共振(NMR)、差示扫描量热法(DSC)和凝胶渗透色谱法(GPC)分析相结合的方法,确定了一系列单体的聚合物结构和链长。从机理上讲,我们推测共催化剂不会原位反应形成氢化铁(II),而是链增长通过活性铁(III)物种进行。我们还进行了动力学和同位素实验以加深理解。此外,还研究了一种非常特殊的1,3 - 取代环丁烷副产物的形成。