Neyyathala Arjun, Flecken Franziska, Rang Fabian, Papke Christina, Hanf Schirin
Karlsruhe Institute of Technology, Institute for Inorganic Chemistry, Engesserstr. 15, 76131, Karlsruhe, Germany.
Chemistry. 2024 Jan 2;30(1):e202302825. doi: 10.1002/chem.202302825. Epub 2023 Nov 8.
Herein we report the use of a supported Pd P catalyst for Heck coupling reactions. For the stabilisation of Pd P and Pd, as reference system, the silica support material was modified via phosphorus doping (0.5 and 1 wt % P). Through this so-called support engineering approach, the catalytic activity of Pd P was clearly enhanced. Whereas an iodobenzene conversion of 79 % was witnessed for Pd P@SiO in the coupling of styrene and iodobenzene in 1 h, 90 % conversion could be achieved using Pd P@1P-SiO . This improved catalytic activity probably stems from an electronic modulation of the support surface via the introduction of phosphorus. Simultaneously, the recyclability was boosted and the Pd P@1P-SiO catalyst has shown to maintain its catalytic activity over several recovery tests. Hereby, metal leaching could almost be suppressed completely to 3 % by the use of a P-modified silica support.
在此,我们报道了一种负载型钯磷催化剂用于Heck偶联反应。作为参考体系,为了稳定钯磷和钯,通过磷掺杂(0.5和1 wt% P)对二氧化硅载体材料进行了改性。通过这种所谓的载体工程方法,钯磷的催化活性明显提高。在苯乙烯与碘苯的偶联反应中,1小时内钯磷@二氧化硅的碘苯转化率为79%,而使用钯磷@1P-二氧化硅可实现90%的转化率。这种提高的催化活性可能源于通过引入磷对载体表面进行的电子调制。同时,可回收性得到了提高,并且钯磷@1P-二氧化硅催化剂在多次回收测试中均显示出保持其催化活性。由此,通过使用磷改性的二氧化硅载体,金属浸出几乎可以完全抑制到3%。