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NiBr(P(CH2CH2P(C6H5)2)3)(1+)*AsF6(1-) = {NiBr(P(CH2CH2P(C6H5)2)3)}AsF6

Base Information
  • Chemical Name:NiBr(P(CH2CH2P(C6H5)2)3)(1+)*AsF6(1-) = {NiBr(P(CH2CH2P(C6H5)2)3)}AsF6
  • CAS No.:99687-63-5
  • Molecular Formula:AsF6*C42H42BrNiP4
  • Molecular Weight:998.197
  • Hs Code.:
NiBr(P(CH<sub>2</sub>CH<sub>2</sub>P(C<sub>6</sub>H<sub>5</sub>)2)3)<sup>(1+)</sup>*AsF<sub>6</sub><sup>(1-)</sup> = {NiBr(P(CH<sub>2</sub>CH<sub>2</sub>P(C<sub>6</sub>H<sub>5</sub>)2)3)}AsF<sub>6</sub>

Synonyms:

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Chemical Property of NiBr(P(CH2CH2P(C6H5)2)3)(1+)*AsF6(1-) = {NiBr(P(CH2CH2P(C6H5)2)3)}AsF6
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Technology Process of NiBr(P(CH2CH2P(C6H5)2)3)(1+)*AsF6(1-) = {NiBr(P(CH2CH2P(C6H5)2)3)}AsF6

There total 1 articles about NiBr(P(CH2CH2P(C6H5)2)3)(1+)*AsF6(1-) = {NiBr(P(CH2CH2P(C6H5)2)3)}AsF6 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 ethanol; dichloromethane; under N2; addn. of a soln. of equimolar amts. of the organic ligand in CH2Cl2 to a soln. of the Ni salt in EtOH with slight excess of LiAsF6; heated at 50°C for 1h; refluxed for 6h; soln. concd., ppt washed with EtOH, Et2O, dried in vac.;;
Guidance literature:
In ethanol; under N2; addn. of excess of phosphite to a stirred soln. of the Ni complex and slight excess of LiAsF6; stirred for 2h; ppt. washed with EtOH, Et2O, dried in vac.;; elem. anal.;;
Guidance literature:
In methanol; under N2; addn. of excess of phosphite to a stirred soln. of the Ni complex and slight excess of LiAsF6; stirred for 2h; ppt. washed with MeOH, Et2O, dried in vac.;; elem. anal.;;
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