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Highly efficient and recyclable ruthenium nanoparticle catalyst for semihydrogenation of alkynes
Ru nanoparticles were used as catalysts for semihydrogenation of alkynes for the first time. Poly(ethylene glycol) (PEG)-stabilized Ru nanoparticles were used as catalysts for semihydrogenation of various terminal alkynes in thermoregulated PEG biphasic system, which allows for not only an efficient...
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Published in: | Catalysis communications 2013-08, Vol.38, p.77-81 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Ru nanoparticles were used as catalysts for semihydrogenation of alkynes for the first time. Poly(ethylene glycol) (PEG)-stabilized Ru nanoparticles were used as catalysts for semihydrogenation of various terminal alkynes in thermoregulated PEG biphasic system, which allows for not only an efficient homogeneous catalytic reaction, but also an easy biphasic separation and reuse of catalyst. Under the optimized conditions, various terminal alkynes were hydrogenated to the corresponding alkenes with high selectivity. After reaction, the Ru nanoparticle catalyst could be separated from products by simple phase separation and recycled for ten times without evident loss in activity and selectivity.
Ru nanoparticles were used as catalysts for semihydrogenation of alkynes for the first time. The polyethylene glycol (PEG)-stabilized Ru nanoparticles in a thermoregulated PEG biphasic system, which leads to a biphasic system at room temperature while homogeneous during catalysis, were active, selective and recyclable catalyst for semihydrogenation of alkynes. [Display omitted]
•Ru nanoparticles were used as catalysts for semihydrogenation of alkynes for the first time.•PEG-stabilized Ru nanoparticles are active, selective and recyclable catalyst for semihydrogenation of alkynes.•The catalytic system can realize a homogeneous reaction coupled with a biphasic separation. |
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ISSN: | 1566-7367 1873-3905 |
DOI: | 10.1016/j.catcom.2013.04.015 |