动力学和热力学偏好在基与基C-H键激活与阳离子Pt (II) 复合物中的动力学和热力学偏好
Alan F Heyduk1, Tom G Driver, Jay A Labinger
1The Arnold and Mabel Beckman Laboratories of Chemical Synthesis, California Institute of Technology, Pasadena, California 91125, USA.
新的无水酸 (((II) 复合物激活了芳香化合物中的C-H键. 这些复合物表现出增强的反应性,并且由于独特的结构中间体,在甲基中有利于基相对于芳香激活.
科学领域:
- 有机金属化学 有机金属化学
- 催化剂是一种催化剂.
- 协调化学 协调化学
背景情况:
- 在合成化学中,C-H键激活至关重要.
- ((II) 复合物是已知的C-H激活的催化剂.
- 无水酸复合物提供了增强反应性的潜力.
研究的目的:
- 为了合成和表征新的无水阴离子Pt (II) 复合物.
- 为了研究这些复合物的C-H键激活能力与arenes.
- 为了比较它们的反应性与现有的白金系统.
主要方法:
- 通过与B(C6F5) 的反应合成无水性阴阳性Pt(II) 复合物3.3.
- 反应产物的光谱表征.
- 对C-H激活反应的动力学和热力学研究.
主要成果:
- 无水离子Pt (II) 复合物[ (NN) Pt (CH3) (CF3CD2OD) ]+已成功制备.
- 这些复合体与水生复合体相比,具有增强的C-H激活反应性.
- 对于甲基,基C-H激活在热力学上比芳香C-H激活更受青.
结论:
- 无水离子Pt(II) 复合物是C-H激活的有效催化剂.
- 对基激活的观察到的偏好归因于稳定的eta3-基中间体的形成.
- 这项研究为控制C-H激活反应中的区域选择性提供了洞察力.
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