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Copper Nanoparticles Catalyzed Se(Te)Se(Te) Bond Activation: A Straightforward Route Towards Unsymmetrical Organochalcogenides from Boronic Acids
Author(s) -
Mohan Balaji,
Yoon Chohye,
Jang Seongwan,
Park Kang Hyun
Publication year - 2015
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201402867
Subject(s) - catalysis , copper , heterogeneous catalysis , chemistry , nanoparticle , boronic acid , activated carbon , ligand (biochemistry) , inorganic chemistry , organic chemistry , combinatorial chemistry , materials science , nanotechnology , adsorption , biochemistry , receptor
A highly porous copper metal–organic framework, [Cu 3 (BTC) 2 ] (BTC=benzene‐1,3,5‐tricarboxylate) was synthesized and used as a precursor for the synthesis of copper nanoparticles (NPs) and characterized by several techniques, including XRD, SEM, TEM, EDX and BET measurements. The as‐synthesized copper nanoparticles were immobilized onto activated charcoal (AC) by means of ultrasonication at room temperature without any pretreatment. The Cu NPs/AC was employed as a heterogeneous catalyst for the cross‐coupling of diphenyl diselenide and boronic acids to form diphenyl selenides through SeSe bond activation under ligand‐, base‐, and additive‐free conditions. The copper NPs/AC, which combines the architecture of MOFs and the high surface area of charcoal, could be an efficient heterogeneous catalytic system that is compatible with a variety of substituents on diphenyl selenides. Its promising catalytic activity relative to that of other homogeneous systems and low catalyst loading for the synthesis of unsymmetrical diaryl selenides is an important application in the area of nanocatalysis. The Cu NPs/AC catalyst, which exhibits excellent catalytic activity and remarkable tolerance to a wide variety of substituents, led to Se sp 3 ‐, sp 2 ‐, and sp‐carbon bond formation by using DMSO as a solvent and atmospheric air as oxidant. This approach can also be extended to the preparation of unsymmetrical organotelluride derivatives.