"氧化诱导"氧化氧气从eta2-peroxopalladium ((II) 复合物中被电子缺陷基促进的减少性消除
Brian V Popp1, Shannon S Stahl
1Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706, USA.
Journal of the American Chemical Society
|March 2, 2006
概括
这项研究报告了首次使用缺乏电子的基从过氧 (II) 复合物中对氧气的关联性取代. 这种反应通过一种关联性连接体替代机制形成了(0) - 化合物.
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.
- 反应机制 反应机制
背景情况:
- 氧 () 复合物是氧化反应中的关键中间体.
- 了解连接体移位机制对于催化剂设计至关重要.
- 缺乏电子的基与金属复合物的反应性具有显著的兴趣.
研究的目的:
- 举报第一个从多氧 (II) 复合体中二氧化碳的关联移位的例子.
- 为了研究反应机制和烯电子性质的影响.
- 为了合成新的(0) - 基复合物.
主要方法:
- 各种p-X-trans-beta-nitrostyrenes与 (bc) Pd ((β2-O2) 的反应 (bc = 巴托库普罗因).
- 由此产生的(0) - 烯复合物的光谱表征.
- 机理学研究以阐明反应途径.
主要成果:
- 缺乏电子的基因从多氧 (II) 复合体中定量取代了氧气.
- 反应通过一种关联性连接体替代机制进行.
- 的电子性质影响了反应路径,与氧化诱导的还原性消除相一致.
结论:
- 从多帕拉 (II) 复合物中对氧气的关联性取代是可行的.
- 这种反应提供了一条新路径,可以产生 ((0)) -烯复合体.
- 这些发现为催化反应的机制提供了洞察力.
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