Kubota Koji, Takahashi Rina, Ito Hajime
Division of Applied Chemistry and Frontier Chemistry Center , Faculty of Engineering , Hokkaido University , Sapporo , Hokkaido , Japan . Email:
Institute for Chemical Reaction Design and Discovery (WPI-ICReDD) , Hokkaido University , Sapporo , Hokkaido , Japan.
Chem Sci. 2019 May 7;10(22):5837-5842. doi: 10.1039/c9sc01711a. eCollection 2019 Jun 14.
Organic reactions that employ moisture- and/or oxygen-sensitive reagents or intermediates usually involve the use of glove-box or Schlenk-line techniques as well as dry and degassed solvents. Unfortunately, these requirements may greatly reduce the utility of the targeted organic molecules. Herein, we demonstrate that solvent-free mechanochemical synthetic techniques allow using highly oxygen-sensitive palladium(0) species in air for the stoichiometric oxidative addition of aryl halides. The low diffusion efficiency of gaseous oxygen in crystalline or amorphous solid-state reaction mixtures should be the main reason for the low impact of the presence of atmospheric oxygen on the sensitive oxidative addition reactions under the applied conditions. This study thus illustrates the outstanding potential of mechanochemistry to serve as an operationally simple, glove-box-and-Schlenk-line-free synthetic route to organometallic compounds and other valuable synthetic targets, even when sensitive reagents or intermediates are involved.
使用对水分和/或氧气敏感的试剂或中间体的有机反应通常需要使用手套箱或施伦克线技术以及干燥和脱气的溶剂。不幸的是,这些要求可能会大大降低目标有机分子的实用性。在此,我们证明无溶剂机械化学合成技术允许在空气中使用对氧气高度敏感的钯(0)物种,用于芳基卤化物的化学计量氧化加成反应。气态氧在结晶或无定形固态反应混合物中的低扩散效率应该是在所应用条件下大气氧的存在对敏感氧化加成反应影响较小的主要原因。因此,本研究说明了机械化学作为一种操作简单、无需手套箱和施伦克线的合成路线来制备有机金属化合物和其他有价值的合成目标的巨大潜力,即使涉及敏感试剂或中间体。