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CoH(P(OC2H5)2(C6H5))4(1+)*B(C6H5)4(1-)=CoH(P(OC2H5)2(C6H5))4B(C6H5)4

Base Information
  • Chemical Name:CoH(P(OC2H5)2(C6H5))4(1+)*B(C6H5)4(1-)=CoH(P(OC2H5)2(C6H5))4B(C6H5)4
  • CAS No.:131629-82-8
  • Molecular Formula:C24H20B*C40H61CoO8P4
  • Molecular Weight:1172.04
  • Hs Code.:
CoH(P(OC<sub>2</sub>H<sub>5</sub>)2(C<sub>6</sub>H<sub>5</sub>))4<sup>(1+)</sup>*B(C<sub>6</sub>H<sub>5</sub>)4<sup>(1-)</sup>=CoH(P(OC<sub>2</sub>H<sub>5</sub>)2(C<sub>6</sub>H<sub>5</sub>))4B(C<sub>6</sub>H<sub>5</sub>)4

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Chemical Property of CoH(P(OC2H5)2(C6H5))4(1+)*B(C6H5)4(1-)=CoH(P(OC2H5)2(C6H5))4B(C6H5)4
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Technology Process of CoH(P(OC2H5)2(C6H5))4(1+)*B(C6H5)4(1-)=CoH(P(OC2H5)2(C6H5))4B(C6H5)4

There total 2 articles about CoH(P(OC2H5)2(C6H5))4(1+)*B(C6H5)4(1-)=CoH(P(OC2H5)2(C6H5))4B(C6H5)4 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 NaB(C6H5)4; In dichloromethane; cooling of a soln. of Co-compd. to -80°C (under Ar, Schlenk app.)and quick addn. to diazonium compd. at the same temp., warming to room temp. in 20 min, shaking for 30-40 min; solvent removal under reduced pressure, then triturating in EtOH, addn. of NaBPH4, crystn. from CH2Cl2/EtOH, elem. anal.;
DOI:10.1039/DT9900002979
Guidance literature:
In acetonitrile; Electrolysis; inert atmosphere, electrolysis of the Co complex at -0.2 V versus SCE in CH3CN containing NaClO4 as supporting electrolyte, Pt and glassy-C electrodes, evapn. to dryness, extn. (CH2Cl2), evapn., oil treated with ethanol, addn. of NaBPh4, pptn.; filtration, crystn. (CH2Cl2 and ethanol), elem. anal.;
DOI:10.1039/DT9940000695
Guidance literature:
In dichloromethane; addn. of an excess of isocyanide to soln. of Co-compd. (under Ar, Schlenk app.), stirring for 30 min; solvent removal under reduced pressure, treating of residue with EtOH, crystn. from EtOH/CH2Cl2, elem. anal.;
DOI:10.1039/DT9900002979
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