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A simple, efficient and recyclable catalytic system for carbon–sulfur coupling of aryl halides with thioacetamide
- Source :
- Journal of Molecular Catalysis A: Chemical. 395:349-354
- Publication Year :
- 2014
- Publisher :
- Elsevier BV, 2014.
-
Abstract
- The carbon–sulfur coupling reaction of aryl halides with thioacetamide using an MCM-41-immobilized bidentate nitrogen copper(I) complex [MCM-41-2N-CuI] as an efficient heterogeneous catalyst is described. Developed catalytic system is found to be effective for the coupling reaction of aryl halides with thioacetamide providing moderate to high yield of diaryl sulfides. This heterogeneous copper catalyst exhibits higher activity than CuI and can be recovered by a simple filtration of the reaction solution and reused for at least 10 consecutive trials without any decreases in activity.
- Subjects :
- chemistry.chemical_classification
Chemistry
Process Chemistry and Technology
Aryl halide
Aryl
Inorganic chemistry
Halide
chemistry.chemical_element
Heterogeneous catalysis
Combinatorial chemistry
Copper
Catalysis
Coupling reaction
chemistry.chemical_compound
Yield (chemistry)
Physical and Theoretical Chemistry
Subjects
Details
- ISSN :
- 13811169
- Volume :
- 395
- Database :
- OpenAIRE
- Journal :
- Journal of Molecular Catalysis A: Chemical
- Accession number :
- edsair.doi...........1120a9659011a548d73490045be13fe6
- Full Text :
- https://doi.org/10.1016/j.molcata.2014.08.010