The author of 《Magnetite tethered mesoionic carbene-palladium (II): An efficient and reusable nanomagnetic catalyst for Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions in aqueous medium》 were Kempasiddhaiah, Manjunatha; Kandathil, Vishal; Dateer, Ramesh B.; Sasidhar, Balappa S.; Patil, Shivaputra A.; Patil, Siddappa A.. And the article was published in Applied Organometallic Chemistry in 2019. Recommanded Product: 623-00-7 The author mentioned the following in the article:
In this paper, a highly active, air- and moisture-stable and easily recoverable magnetic nanoparticles tethered mesoionic carbene palladium(II) complex (MNPs-MIC-Pd) as nanomagnetic catalyst was successfully synthesized by a simplistic multistep synthesis under aerobic conditions using com. available inexpensive chems. for the first time. The prepared MNPs-MIC-Pd nanomagnetic catalyst was used to catalyze the Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions and exhibited excellent catalytic activity for various substrates under mild reaction conditions. Moreover, MNPs-MIC-Pd nanomagnetic catalyst could be easily and rapidly recovered by applying an external magnet. The recovered MNPs-MIC-Pd nanomagnetic catalyst exhibited very good catalytic activity up to ten times in Suzuki-Miyaura and five times in Mizoroki-Heck cross-coupling reactions without considerable loss of its catalytic activity. However, MNPs-MIC-Pd nanomagnetic catalyst shows notable advantages such as heterogeneous nature, efficient catalytic activity, mild reaction conditions, easy magnetic work up and recyclability. In addition to this study using 4-Bromobenzonitrile, there are many other studies that have used 4-Bromobenzonitrile(cas: 623-00-7Recommanded Product: 623-00-7) was used in this study.
4-Bromobenzonitrile(cas: 623-00-7) has been used in the synthesis of 4-iodobenzonitrile via photo-induced aromatic Finkelstein iodination reaction.Recommanded Product: 623-00-7 It can also be used as an aryl halide test compound in developing greener reaction conditions for Suzuki cross-coupling between aryl halides and phenyl boronic acid.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts