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RuH(CO)(C5H4NCN)2(As(C6H5)3)2(1+)*PF6(1-)=(RuH(CO)(C5H4NCN)2(As(C6H5)3)2)PF6

Base Information
  • Chemical Name:RuH(CO)(C5H4NCN)2(As(C6H5)3)2(1+)*PF6(1-)=(RuH(CO)(C5H4NCN)2(As(C6H5)3)2)PF6
  • CAS No.:131931-10-7
  • Molecular Formula:C49H39As2N4ORu*F6P
  • Molecular Weight:1095.75
  • Hs Code.:
RuH(CO)(C<sub>5</sub>H<sub>4</sub>NCN)2(As(C<sub>6</sub>H<sub>5</sub>)3)2<sup>(1+)</sup>*PF<sub>6</sub><sup>(1-)</sup>=(RuH(CO)(C<sub>5</sub>H<sub>4</sub>NCN)2(As(C<sub>6</sub>H<sub>5</sub>)3)2)PF<sub>6</sub>

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Chemical Property of RuH(CO)(C5H4NCN)2(As(C6H5)3)2(1+)*PF6(1-)=(RuH(CO)(C5H4NCN)2(As(C6H5)3)2)PF6
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Technology Process of RuH(CO)(C5H4NCN)2(As(C6H5)3)2(1+)*PF6(1-)=(RuH(CO)(C5H4NCN)2(As(C6H5)3)2)PF6

There total 1 articles about RuH(CO)(C5H4NCN)2(As(C6H5)3)2(1+)*PF6(1-)=(RuH(CO)(C5H4NCN)2(As(C6H5)3)2)PF6 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In methanol; benzene; heating of a soln. of 4-CNPy and Ru-complex in C6H6 under reflux for 4.5 h, cooling to room temp., filtration, concentration under reduced pressure (vol. to ca 5 cm**3), addn. of a soln. of the suitable anion salt in CH3OH, crystn. during 10 h; centrifugation, washing with CH3OH, then H2O, then CH3OH, then diethyl ether, drying in vac.; elem. anal.;
DOI:10.1016/S0277-5387(00)84047-4
Guidance literature:
In methanol; heating of a suspn. of Ru-NCPy-complex and Ru-C5H5-complex in CH3OH under reflux for ca 5 h, cooling to room temp., filtration, concentration under reduced pressure (vol. to ca 5 cm**3), addn. of a soln. of the suitable anion salt in CH3OH; sepn. of crystalline compd. by filtration, washing with CH3OH, then H2O, then CH3OH, then diethyl ether, drying in vac.; elem. anal.;
DOI:10.1016/S0277-5387(00)84047-4
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