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C-N-palladacyclic-catalyzed Heck reaction in EGME/water: Rate and regioselectivity controlled by the solvents ratio

机译:EGME /水中C-N-四环环催化的Heck反应:速率和区域选择性受溶剂比率控制

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摘要

Novel as well as known C, N-palladacyclic neutral complexes were tested as precatalyst in the Heck reaction between bromobenzene and styrene under aerobic conditions. The catalytic system Pd(II) complex/K2CO3/EGME-H2O (EGME = ethylene glycol monomethyl ether) showed to be highly efficient. Best performances of the catalysts were achieved by controlling the amount of water: generally a H2O content within the 25-50% v/v range resulted in the highest conversion of the substrates into trans-stilbene. As a matter of fact, bromobenzene and styrene can be converted quantitatively using only 0.01 mol% of precatalyst with very high regioselectivity for the trans product and with a TOF of 10000 h (1). In the absence of water, all complexes were less efficient and differences in their activity were found, while such a differentiation disappeared when water was added.
机译:在好氧条件下,在溴苯和苯乙烯之间的Heck反应中,测试了新型的和已知的C,N-四环中性配合物作为前催化剂。 Pd(II)络合物/ K2CO3 / EGME-H2O(EGME =乙二醇单甲醚)催化体系显示出很高的效率。通过控制水量可以达到催化剂的最佳性能:通常H2O含量在25-50%v / v范围内会导致底物向反式二苯乙烯的转化率最高。事实上,仅使用0.01 mol%的前催化剂即可对溴苯和苯乙烯进行定量转化,该催化剂对反式产物的区域选择性很高,TOF为10000 h(1)。在没有水的情况下,所有复合物的效率均较低,并且发现它们的活性存在差异,而加入水后这种差异消失了。

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