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[closo-1-Ph-3,8-(PPh3)2-3-Cl-3-H-3,1,2-RhC2B9H9]*0.5(benzene)

Base Information
  • Chemical Name:[closo-1-Ph-3,8-(PPh3)2-3-Cl-3-H-3,1,2-RhC2B9H9]*0.5(benzene)
  • CAS No.:89462-05-5
  • Molecular Formula:C44H45B9ClP2Rh
  • Molecular Weight:910.503
  • Hs Code.:
[closo-1-Ph-3,8-(PPh<sub>3</sub>)2-3-Cl-3-H-3,1,2-RhC<sub>2</sub>B<sub>9</sub>H<sub>9</sub>]*0.5(benzene)

Synonyms:[closo-1-Ph-3,8-(PPh3)2-3-Cl-3-H-3,1,2-RhC2B9H9]*0.5(benzene)

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Chemical Property of [closo-1-Ph-3,8-(PPh3)2-3-Cl-3-H-3,1,2-RhC2B9H9]*0.5(benzene)
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Technology Process of [closo-1-Ph-3,8-(PPh3)2-3-Cl-3-H-3,1,2-RhC2B9H9]*0.5(benzene)

There total 3 articles about [closo-1-Ph-3,8-(PPh3)2-3-Cl-3-H-3,1,2-RhC2B9H9]*0.5(benzene) 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:
With triphenylphosphine; HBF4; benzene; In ethanol; water; to mixt. of educts and PPh3 added EtOH followed by 48% aq. HBF4, heatedto reflux temp. for 7 h, allowed to cool to ca. 40°C; ppt. isolated by filtration, washed with EtOH and Et2O, recrystd. from benzene/EtOH; elem. anal.;
DOI:10.1021/ja00322a038
Guidance literature:
With CH2Cl2; In n-heptane; dichloromethane; recrystd. by layering heptane over CH2Cl2 soln. of Rh complex; crystals sepd. mechanically;
DOI:10.1021/ja00322a038
Guidance literature:
In dichloromethane-d2; keeping educt in CD2Cl2 soln. for several months; detected by NMR;
DOI:10.1021/ja00322a038
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