卢提丁/B(C6F5)3:在经典和挫败的易斯对反应性的边界
Stephen J Geier1, Douglas W Stephan
1Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, Canada, M5S 3H6.
Journal of the American Chemical Society
|February 27, 2009
概括
经典的易斯酸添加物,以前被认为是不反应的,现在可以用于挫败的易斯对化学. 这项研究表明它们能够激活气并打开THF环的能力.
科学领域:
- * 无机化学 无机化学
- * 有机金属化学
背景情况:
- * 经典的易斯酸添加物通常被认为是稳定且不反应的物种.
- * 丧的易斯对 (FLP) 具有独特的反应性,这是由于硬质障碍阻止了 adduct 形成.
研究的目的:
- * 为了研究经典的易斯酸 adducts 的反应性.
- * 为了证明这些引证可以访问挫败的易斯对的独特反应性特征.
主要方法:
- * 2,6-路易丁 (一个易斯基) 和B(C6F5) 3 (一个易斯酸) 之间形成添加物.
- *平衡性研究,以描述形的特征.
- * 涉及H2和四氨酸 (THF) 的反应性研究.
主要成果:
- * 在2,6-lutidine/B(C6F5) 3附和自由成分之间建立了平衡.
- * adduct 证明了分子 (H2) 的异解激活.
- * 引证成功引发了THF的环开放.
结论:
- * 经典的易斯酸添加物不一定是不反应的.
- * 这些引证可以作为挫败的易斯对类反应性的前体.
- * 这一发现扩大了易斯酸化学和FLP应用的范围.
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