410538-83-9

Upstream product

• 366-18-7 [2,2]bipyridinyl 
• 410538-79-3 trans-PtCl(p-tolyl)(diethyl sulfide)2 
• 64827-19-6 bis[di(p-tolyl)(μ-diethyl sulfide)platinum(II)] 

Downstream Products

• 1042139-01-4 (2,2'-bipyridine)(2-(5-bromothienyl))(4-methylphenyl)platinum(II) 
• 1042139-04-7 (2,2'-bipyridine)(2-benzothienyl)(4-methylphenyl)platinum(II) 
• 1042139-02-5 (2,2'-bipyridine)(2-(5-formylthienyl))(4-methylphenyl)platinum(II) 
• 1042139-03-6 (2,2'-bipyridine)(2-(5-ethoxycarbonylthienyl))(4-methylphenyl)platinum(II) 
• 1042139-00-3 (2,2'-bipyridine)(2-(4,5-dibromothienyl))(4-methylphenyl)platinum(II) 

Relevant academic research and scientific papers

Mono(p-tolyl)platinum(II) and bis(p-tolyl)platinum(II) complexes of diethylsulfide as reagents for organoplatinum synthesis. Structures of [Pt(p-Tol)2(μ-SEt2)]2 and PtCl(p-Tol)(bpy) (bpy=2,2′-bipyridine)

The complex trans-PtCl(p-Tol)(SEt2)2 is obtained from the reaction of [Pt(p-Tol)2(SEt2)]2 with PtCl2(SEt2)2 and SEt2 in mole ratio 1:2:2. The mono(p-tolyl)platinum(II) and bis(p-tolyl)platinum(II) complexes of diethylsulfide react with 2,2′-bipyridine to form the complexes PtX(p-Tol)(bpy) (X=p-Tol, Cl) and are useful reagents for organoplatinum chemistry. X-ray crystal structures are presented for square planar PtCl(p-Tol)(bpy) and the centrosymmetric dimer [Pt(p-Tol)2(μ-SEt2)]2. 2002 Published by Elsevier Science B.V.