分子氧的Pd介导激活:Pd(0) 与直接插入相比
Jason M Keith1, William A Goddard, Jonas Oxgaard
1Materials Process and Simulation Center, MC (139-74), California Institute of Technology, Pasadena, California 91125, USA.
Journal of the American Chemical Society
|August 7, 2007
概括
这项研究阐明了分子氧与化复合物的反应机制,揭示了通过Pd(0) 和直接插入的途径. 直接插入是环境友好的化学开发的首选.
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
- 绿色化学 绿色化学
背景情况:
- 开发对环境无害的化学品需要直接使用二氧化.
- 使用二氧化物的直接氧化通常是不切实际的,需要机械的理解.
- 化复合物是催化循环中的关键中间体.
研究的目的:
- 阐明分子氧的反应机制与溶化化合物复合物.
- 专注于通过Pd(0) 的路径,并与直接插入进行比较.
- 提供化与分子氧的再氧化途径的完整映射.
主要方法:
- 量子力学计算 (使用PBF溶剂模型的B3LYP/LACVP**).
- 在基的存在下对Pd (II-) (H) (Cl) 的研究.
- 对旋转过渡和反应完成的分析.
主要成果:
- 确定了一个最低屏障Pd(0) 路径,涉及基辅助去质子化,O2联结和损失.
- 形成一个eta(2)-peroxo-palladium复合物的特征.
- 对于研究的系统来说,确定直接插入的途径是首选的 (DeltaDeltaH++ = 6.2 kcal/mol,DeltaDeltaG++ = 7.5 kcal/mol).
结论:
- 斯帕特因的双边性质和缺乏pi-接受联结体有利于直接插入.
- 了解这些机制有助于开发实际的直接氧化与二氧化物.
- 提供了建议,以切换路径偏好.
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