Home > Publications database > Bimetallic Co/Al nanoparticles in an ionic liquid: synthesis and application in alkyne hydrogenation > print |
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100 | 1 | _ | |a Schmolke, Laura |0 0000-0002-2369-9331 |b 0 |
245 | _ | _ | |a Bimetallic Co/Al nanoparticles in an ionic liquid: synthesis and application in alkyne hydrogenation |
260 | _ | _ | |a London |c 2019 |b RSC |
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520 | _ | _ | |a Herein, we report the microwave-induced decomposition of various organometallic cobalt and aluminum precursors in an ionic liquid (IL), 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIm]NTf2), resulting in Co/Al nanoalloys with different molar Co/Al ratios. The dual-source precursor system of dicobalt octacarbonyl (Co2(CO)8) and pentamethylcyclopentadienyl aluminum ([AlCp*]4) in [BMIm]NTf2 afforded CoAl nanoparticles (CoAl-NPs) with a molar Co/Al ratio of 1 : 1. Their size and size distribution were determined via transmission electron microscopy (TEM) to be an average diameter of 3.0 ± 0.5 nm. Furthermore, the dual-source precursor system of cobalt amidinate ([Co(iPr2-MeAMD)2]) and aluminum amidinate [Me2Al(iPr2-MeAMD)] in molar ratios of 1 : 1 and 3 : 1 resulted in CoAl- and Co3Al-NPs with an average diameter of 3 ± 1 and 2.0 ± 0.2 nm, respectively. All the obtained materials were characterized via TEM, energy dispersive X-ray spectroscopy (EDX), selected area electron diffraction (SAED), together with high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and (high-resolution) X-ray photoelectron spectroscopy ((HR-)XPS). Phase-pure Co/Al-NPs were not obtained since the concomitant formation of Co-NPs and Al2O3 occurred in this wet-chemical synthesis. The as-prepared Co/Al nanoalloys were evaluated as catalysts in the hydrogenation of phenylacetylene under mild conditions (2 bar H2, 30 °C in THF). In comparison to the monometallic Co-NPs, the Co/Al-NPs showed a significantly higher catalytic hydrogenation activity. The Co- and Co/Al-NPs were also active under harsher reaction conditions (80 bar H2, 80 °C) without the addition of the activating co-catalyst DIBAL-H. |
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700 | 1 | _ | |a Gregori, Bernhard J. |0 P:(DE-HGF)0 |b 1 |
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700 | 1 | _ | |a Schmitz, Alexa |0 0000-0002-1075-4194 |b 3 |
700 | 1 | _ | |a Barthel, Juri |0 P:(DE-Juel1)130525 |b 4 |
700 | 1 | _ | |a Staiger, Lena |0 P:(DE-HGF)0 |b 5 |
700 | 1 | _ | |a Fischer, Roland A. |0 0000-0002-7532-5286 |b 6 |
700 | 1 | _ | |a Jacobi von Wangelin, Axel |0 0000-0001-7462-0745 |b 7 |e Corresponding author |
700 | 1 | _ | |a Janiak, Christoph |0 0000-0002-6288-9605 |b 8 |e Corresponding author |
773 | _ | _ | |a 10.1039/C9NJ03622A |g Vol. 43, no. 42, p. 16583 - 16594 |0 PERI:(DE-600)1472933-7 |n 42 |p 16583 - 16594 |t New journal of chemistry |v 43 |y 2019 |x 1369-9261 |
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