Khoshsefat Mostafa, Ma Yanping, Sun Wen-Hua
Graduate School of Advanced Science and Technology, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi 923-1292, Ishikawa, Japan.
Key Laboratory of Engineering Plastics and Beijing National Laboratory for Molecular Science, Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, China.
Materials (Basel). 2025 May 5;18(9):2123. doi: 10.3390/ma18092123.
Recent advances in designing multinuclear late transition metal catalysts for the oligo-/polymerization of olefins emphasize the great interest and promising approaches in the preparation and application of these catalytic systems. Accordingly, in this study, two dinuclear macrocyclic bis(iminopyridine) Fe- and Co-based complexes (FC and CC) were prepared at moderate yields through a one-pot template reaction. Upon activation by MMAO, not only did the catalysts show reasonable activities for the oligomerization of ethylene but also showed high selectivity for the production of tetramers (α-C). With respect to the catalyst structure, FC demonstrated higher catalyst activity (9.45 g mol Fe h × 10 vs. 8.75 × 10 g mol Co h) along with higher selectivity for α-C production compared to CC (96.6 vs. 96.1%). Both catalysts had thermal stability up to 70 °C, with FC being much more active and stable than CC under identical conditions. On the other hand, polymerization parameters had an influence on the catalyst performance and oligomer distribution. Moreover, molecular calculations were employed for geometry optimization and structural determination, which was consistent with the experimental results.
设计用于烯烃低聚/聚合的多核后过渡金属催化剂的最新进展突显了人们对这些催化体系的制备和应用的浓厚兴趣以及颇具前景的方法。因此,在本研究中,通过一锅法模板反应以中等产率制备了两种双核大环双(亚氨基吡啶)铁基和钴基配合物(FC和CC)。经MMAO活化后,这些催化剂不仅对乙烯低聚显示出合理的活性,而且对四聚体(α-C)的生产表现出高选择性。就催化剂结构而言,与CC相比,FC表现出更高的催化剂活性(9.45 g mol Fe h × 10 对 8.75 × 10 g mol Co h)以及对α-C生产更高的选择性(96.6% 对 96.1%)。两种催化剂在高达70 °C的温度下均具有热稳定性,在相同条件下FC比CC更具活性和稳定性。另一方面,聚合参数对催化剂性能和低聚物分布有影响。此外,采用分子计算进行几何优化和结构测定,这与实验结果一致。