[(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)]

Base Information

Chemical Name:[(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)]
CAS No.:474645-03-9
Molecular Formula:C₂₆H₃₈N₂Pt
Molecular Weight:573.681
Hs Code.:

Synonyms:[(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)]

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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 [(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)]

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Technology Process of [(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)]

There total 1 articles about [(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)] 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: 85.0%

: bis(dimethyl sulfoxide)-dimesitylplatinum(II)

: 28227-41-0,24764-90-7
1,4-diisopropyl-1,4-diazabuta-1,3-diene

: 474645-03-9
[(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)]

Guidance literature:: In toluene; ((dmso)2Pt(Mes)2) and ligand (1:2) were suspended in toluene and stirredfor 72 h at 393 K; react. mixt. was evapd. to dryness, residue was extd. with CH2Cl2, and crystd. from CH2Cl2/heptane (1:3); elem. anal.;
DOI:10.1021/ic025547o

Reference yield: 97.0%

: 474645-03-9
[(N,N'-diisopropyl-1,4-diazabutadiene)bis(2,4,6-trimethylphenyl)platinum(II)]

: 75-36-5
acetyl chloride

: 893444-56-9
PtCl(2,4,6-trimethylphenyl)(N,N-diisopropyl-diazabutadiene)

Guidance literature:: With MeOH; In methanol; under Ar or N2, in situ generated up to 5 equiv. of HCl from AcCl and MeOH, with protection from intense light; elem. anal.;
DOI:10.1002/zaac.200500106