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1,2,3,4,5-pentamethylcyclopentadienyliridium(III) chloride bis(2,4,6-trimethylphenylimino)acenapthene tetrafluoroborate - water-dichloromethane - methanol (1/1/1/1)

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  • Chemical Name:1,2,3,4,5-pentamethylcyclopentadienyliridium(III) chloride bis(2,4,6-trimethylphenylimino)acenapthene tetrafluoroborate - water-dichloromethane - methanol (1/1/1/1)
  • CAS No.:1000700-19-5
  • Molecular Formula:BF4*CH2Cl2*CH4O*C40H43ClIrN2*H2O
  • Molecular Weight:1001.26
  • Hs Code.:
  • Mol file:1000700-19-5.mol
1,2,3,4,5-pentamethylcyclopentadienyliridium(III) chloride bis(2,4,6-trimethylphenylimino)acenapthene tetrafluoroborate - water-dichloromethane - methanol (1/1/1/1)

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Chemical Property of 1,2,3,4,5-pentamethylcyclopentadienyliridium(III) chloride bis(2,4,6-trimethylphenylimino)acenapthene tetrafluoroborate - water-dichloromethane - methanol (1/1/1/1) Edit
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Technology Process of 1,2,3,4,5-pentamethylcyclopentadienyliridium(III) chloride bis(2,4,6-trimethylphenylimino)acenapthene tetrafluoroborate - water-dichloromethane - methanol (1/1/1/1)

There total 1 articles about 1,2,3,4,5-pentamethylcyclopentadienyliridium(III) chloride bis(2,4,6-trimethylphenylimino)acenapthene tetrafluoroborate - water-dichloromethane - methanol (1/1/1/1) 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; toluene; further educts; (inert atm.), suspn. of Ir complex in toluene stirred for 30 min, treated with 2 equiv. of ligand in toluene, stirred for 30 min, treated dropwise with 2 equiv. of NaBF4 in CH3OH/toluene (1:4), stirred overnight; concd.(vac.), recrystd.(CH2Cl2/pentane), collected, washed (pentane), dried, elem. anal.;
DOI:10.1002/ejic.200600735
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