关于金属和配体替代对乙烯聚合物的氧胺催化剂反应性的DFT洞察力
Pavee Apilardmongkol1, Manussada Ratanasak2, Jun-Ya Hasegawa2
1Center of Excellence in Computational Chemistry (CECC), Department of Chemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, 10330, Thailand.
这项研究使用了DFT计算来研究由氧胺 (FI) 连接体催化的乙烯聚合. 第二个乙烯插入是决定速度的步骤, (O,S) 连接物显示了改善催化剂活性的潜力.
科学领域:
- 催化剂是一种催化剂.
- 有机金属化学 有机金属化学
- 计算化学的计算化学
背景情况:
- 氧胺 (FI) 连接体在催化过程中至关重要.
- 了解反应机制是催化剂设计的关键.
- 乙烯聚合是一种基本的工业过程.
研究的目的:
- 阐明由FI配体催化乙烯聚合的反应机制.
- 研究过渡金属替代物 (Ti,Zr,Hf) 对催化剂活性的影响.
- 探索用于增强催化性能的配体修饰.
主要方法:
- 使用密度函数理论 (DFT) 的计算.
- 对反应路径和过渡状态的分析.
- 对不同金属中心和连接体的激活能量的比较.
主要成果:
- 同位体A (八面体,cis-N/trans-O/cis-Cl) 是最稳定的反应前的Ti-FI二化物复合体.
- 第二个乙烯插入是决定速度的步骤.
- 激活能量跟随Zr < Hf < Ti,与实验数据保持一致.
- 结合体置换显示 (O,S) 是最有前途的活性.
- 激活能量与Ti-X键距离相关.
- 一种新的基于Ni的FI催化剂在正方形平面几何中显示出更高的活性.
结论:
- 该研究提供了对M-FI催化乙烯聚合机制的基本见解.
- 连接体和金属中心的修改可以调整催化活性.
- (O,S) 配体和特定的金属选择为开发改进的FI催化剂提供了途径.
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