Premium
Nitro group reduction and Suzuki reaction catalysed by palladium supported on magnetic nanoparticles modified with carbon quantum dots generated from glycerol and urea
Author(s) -
Gholinejad Mohammad,
Zareh Fatemeh,
Nájera Carmen
Publication year - 2018
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.3984
Subject(s) - chemistry , palladium , catalysis , suzuki reaction , phenylboronic acid , aryl , nitro , reducing agent , coupling reaction , nuclear chemistry , aryl halide , inorganic chemistry , organic chemistry , alkyl
Glycerol and urea were used as green and cheap sources of carbon quantum dots (CQD) for modifying Fe 3 O 4 nanoparticles (NPs). The obtained CQD@Fe 3 O 4 NPs were used for the stabilization of palladium species and the prepared catalyst, Pd@CQD@Fe 3 O 4 , was characterized using various techniques. This magnetic supported palladium was applied as an efficient catalyst for the reduction of aromatic nitro compounds to primary amines at room temperature using very low palladium loading (0.008 mol%) and also for the Suzuki–Miyaura cross‐coupling reaction of aryl halides as well as challenging heteroaryl bromides and aryl diazonium salts with arylboronic acids and with potassium phenyltrifluoroborate. This magnetically recyclable catalyst was recovered and reused for seven consecutive runs in the reduction of 4‐nitrotoluene to p ‐toluidine and for ten consecutive runs in the reaction of 4‐iodoanisole with phenylboronic acid with small decrease of activity. The catalyst reused in the Suzuki reaction was characterized using transmission electron microscopy, vibrating sample magnetometry and X‐ray photoelectron spectroscopy. Using experiments such as hot filtration and poisoning tests, it has been shown that the true catalyst works under homogeneous conditions according to the release–return pathway of active palladium species.