[Pt(bis(diphenylphosphino)ferrocenyl)(C₂-1,4,5,8-naphthalenediimide)2]

Base Information

Chemical Name:[Pt(bis(diphenylphosphino)ferrocenyl)(C₂-1,4,5,8-naphthalenediimide)2]
CAS No.:928161-47-1
Molecular Formula:C₉₄H₇₈FeN₄O₈P₂Pt
Molecular Weight:1704.55
Hs Code.:

[Pt(bis(diphenylphosphino)ferrocenyl)(C<sub>2</sub>-1,4,5,8-naphthalenediimide)2]

Synonyms:

Suppliers and Price of [Pt(bis(diphenylphosphino)ferrocenyl)(C₂-1,4,5,8-naphthalenediimide)2]

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of [Pt(bis(diphenylphosphino)ferrocenyl)(C₂-1,4,5,8-naphthalenediimide)2]

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of [Pt(bis(diphenylphosphino)ferrocenyl)(C₂-1,4,5,8-naphthalenediimide)2]

There total 1 articles about [Pt(bis(diphenylphosphino)ferrocenyl)(C₂-1,4,5,8-naphthalenediimide)2] 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: 50.0%

: 926643-77-8
N-(4’-ethynylphenyl)-N’-(octyl)naphthalene-1,8:4,5-tetracarboxydiimide

: 75-09-2
dichloromethane

: [Pt(bis(diphenylphosphino)ferrocenyl)Cl₂]*0.4CH₂Cl₂

: 928161-47-1
[Pt(bis(diphenylphosphino)ferrocenyl)(C₂-1,4,5,8-naphthalenediimide)2]

Guidance literature:: copper(l) iodide; In dichloromethane; under N2; Pt complex and excess of ligand in mixt. of CH2Cl2 and i-Pr2NHwere sonicated for 1 h and stirred for 48 h at room temp.; mixt. was diluted with CH2Cl2 and extd. with water, organic phase was sepd., dried with MgSO4, evapd. to dryness, residue was chromd. (SiO2, 0.5% CH3OH in CH2Cl2), fraction was reduced in volume, ppt. was obtained byether addition; elem. anal.;
DOI:10.1016/j.jorganchem.2006.10.060