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(bis(diphenylphosphino)propane)(1,2-benzenedithiolato)platinum(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145360-46-9

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145360-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145360-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,3,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145360-46:
(8*1)+(7*4)+(6*5)+(5*3)+(4*6)+(3*0)+(2*4)+(1*6)=119
119 % 10 = 9
So 145360-46-9 is a valid CAS Registry Number.

145360-46-9Downstream Products

145360-46-9Relevant academic research and scientific papers

Base-promoted synthesis of monometallic and bimetallic platinum complexes containing chelating O,O- or S,S-donor ligands

Praingam, Ngamjit,Anderson, Gordon K.,Rath, Nigam P.

, p. 1767 - 1770 (2008/10/09)

Dichloroplatinum complexes [PtCl2L2] (L2 = cod, dppp) react with 1,2-C6H4E2 (E = O, S) in the presence of a base to produce mononuclear complexes. The diene was not readily displaced from [Pt(E2C6H4-EE)(cod)]. A second approach to complexes containing dianionic chelating ligands involved [Pt(acac)2] as precursor. Reaction with dppp and oxalic acid gave [Pt(C2O4)(dppp)], whereas the analogous reaction with Ph2PC{triple bond, long}CPPh2 produced the bimetallic complex [Pt(C2O4-OO)(μ-Ph2PC{triple bond, long}CPPh2)]2. Similar reactions with 1,2-C6H4E2 (E = O, S) also gave bimetallic products. The structures of [Pt(C2O4)(dppp)] and [Pt(C2O4-OO)(μ-Ph2PC{triple bond, long}CPPh2)]2 have been determined by X-ray crystallography.

Synthesis, reactions, and 31P NMR analysis of (diphosphine)platinum dithiolates

Fazlur-Rahman,Verkade

, p. 5331 - 5335 (2008/10/08)

The reaction between (diphosphine)PtCl2 (diphosphine = dppm, dppe, dppp, dppb, dcpe, depe) and bifunctional thiols (1,2-ethanedithiol, 1,3-propanedithiol, 1,2-benzenedithiol) in acetone or CH2Cla gives the corresponding dithiolate complexes (1-18) in the presence of a base. These thiolato complexes have been isolated as crystalline solids in 57-88% yields and were characterized by 1H, 13C, and 31P NMR spectroscopy. The 31P chemical shifts of these complexes are dependent on both the nature of the diphosphine and the chelating nature of the dithiolato ligand. Treatment of (depe)Pt(SC6H4-o-S) (15) and the analogous dcpe complex (18) with 1 equiv of MeI, allyl chloride, or Me3OBF4 gave the corresponding sulfur-monoalkylated product. Reaction of Cr(nbd)(CO)4 with (depe)PtSC6H4-o-S (15) gave (depe)Pt(SC6H4-o-S)(Cr(CO)4 (22) in 64% yield.

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