[UO₂(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)]

Base Information

• Chemical Name: [UO₂(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)]
• CAS No.: 1155414-67-7
• Molecular Formula: C₃₉H₅₉N₃O₄U
• Molecular Weight: 871.944

Synonyms:[UO₂(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)]

Chemical Property of [UO₂(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)]

Chemical Property:

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Technology Process of [UO₂(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)]

There total 1 articles about [UO₂(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)] 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:

[UO2(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)][Cp(*)2Co] → bis(pentamethylcyclopentadienyl)cobalt(II) (74507-62-3) + [UO2(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)] (1155414-67-7)

Guidance literature:

In toluene; (Ar); dissolution in toluene;

DOI:10.1021/ja9037164

Reference yield:

bis(pentamethylcyclopentadienyl)cobalt(II) (74507-62-3) + [UO2(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)] (1155414-67-7) → [UO2(N,N'-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-bis(methylamino)ethane(-2H))(pyridine)][Cp(*)2Co]

Guidance literature:

In pyridine; (Ar); Co complex added to a soln. of U complex, stirred for 16 h at roomtemp.; filtered, concd., crystd. at -20°C for 16 h; obtained as a mixt.;

DOI:10.1021/ja9037164

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