Paper
Dalton Transactions
Pt1Ru2. 1st step: 164 mg (0.3 mmol) of [Pt2(dba)3] and autoclave was cooled to room temperature and depressurised.
40 mL of toluene. 2nd step: 187 mg (0.60 mmol) of [Ru(COD)- The reaction mixture was then analysed by gas
(COT)]; 43 μL (0.22 mmol) of PPP and 180 mL of THF. Yield: chromatography.
114.8 mg. ICP analysis Ru: 35.5%, Pt: 19.5%.
Pt1Ru4. 1st step: 98 mg (0.18 mmol) of [Pt2(dba)3] and
24 mL of toluene. 2nd step: 227 mg (0.72 mmol) of [Ru(COD)-
(COT)]; 43 μL (0.22 mmol) of PPP and 180 mL of THF. Yield:
90.1 mg. ICP analysis Ru: 56.7%, Pt: 3.4%.
Acknowledgements
Ru/PPP. 284 mg (0.9 mmol) of the [Ru(COD)(COT)] complex This work was supported by the Centre National de la
were introduced into a Fisher-Porter reactor and dissolved with Recherche Scientifique (CNRS), which we gratefully acknowl-
80 mL of THF previously degassed by three freeze–pump edge. We thank the Chinese Scholarship Council (CSC) for the
cycles. The resulting yellow solution was cooled at −60 °C and X. Q. grant. V. Collière (LCC and UPS-TEMSCAN) and L. Datas
a PPP/THF solution (43 μL (0.22 mmol) per 100 mL) was (UPS-TEMSCAN) are also acknowledged for TEM/HRTEM
added to the reactor. The reactor was pressurized with 3 bar of facilities.
H2 and the solution was left to reach slowly the room tempera-
ture. The solution, which turned black after 20 min of reac-
tion, was kept under stirring overnight at room temperature.
After this period of time the Fisher-Porter bottle was depres-
surized and the volume of solvent was reduced to 10 mL under
References
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and filtered again before drying under vacuum. Yield: 88 mg.
ICP analysis Ru: 53.1%.
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9294 | Dalton Trans., 2014, 43, 9283–9295
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