(1,5-cyclooctadiene)((diphenylphosphino)ethyl diphenylphosphinite)iridium(I) tetrafluoroborate1/2CH2Cl2%(Ir(cod)(pop))BF41/2CH2Cl2

Base Information

Chemical Name:(1,5-cyclooctadiene)((diphenylphosphino)ethyl diphenylphosphinite)iridium(I) tetrafluoroborate*1/2CH2Cl2%(Ir(cod)(pop))BF4*1/2CH2Cl2
CAS No.:87556-62-5
Molecular Formula:BF₄*0CH₂Cl₂*C₃₄H₃₆IrOP₂
Molecular Weight:844.098
Hs Code.:

(1,5-cyclooctadiene)((diphenylphosphino)ethyl diphenylphosphinite)iridium(I) tetrafluoroborate*1/2CH2Cl2%(Ir(cod)(pop))BF4*1/2CH2Cl2

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1,5-cyclooctadiene)((diphenylphosphino)ethyl diphenylphosphinite)iridium(I) tetrafluoroborate*1/2CH2Cl2%(Ir(cod)(pop))BF4*1/2CH2Cl2

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Technology Process of (1,5-cyclooctadiene)((diphenylphosphino)ethyl diphenylphosphinite)iridium(I) tetrafluoroborate*1/2CH2Cl2%(Ir(cod)(pop))BF4*1/2CH2Cl2

There total 1 articles about (1,5-cyclooctadiene)((diphenylphosphino)ethyl diphenylphosphinite)iridium(I) tetrafluoroborate*1/2CH2Cl2%(Ir(cod)(pop))BF4*1/2CH2Cl2 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:

Reference yield:

: 32679-03-1
[Ir(1,5-cyclooctadiene)(NCCH₃)₂]BF₄

: 32309-62-9
(diphenylphosphino)ethyl diphenylphosphinite

: 87556-62-5
(1,5-cyclooctadiene)((diphenylphosphino)ethyl diphenylphosphinite)iridium(I) tetrafluoroborate*1/2CH2Cl2%(Ir(cod)(pop))BF4*1/2CH2Cl2

Guidance literature:: With dichloromethane; In dichloromethane; benzene; under inert atm. to soln. (Ir(cod)(MeCN)2)BF4 in CH2Cl2 at -78°Cadded dropwise pop in benzene and soln. stirred at -78°C for 30 min and then at room temp. for 1 h; volume soln. reduced in vacuo, product isolated with Et2O, washed with Et2O and dried in vacuo; elem. anal.;