61250-65-5

Upstream product

• 56-34-8 tetraethylammonium chloride 
• 106373-22-2 bis-μ-bis(diphenylphosphino)methane-μ-hydrido-bis-[chloroplatinum(II)] chloride 
• 1184-78-7 trimethylamine-N-oxide 
• 63910-98-5 bis-μ-bis(diphenylphosphino)methane-μ-hydrido-bis-[hydridoplatinum(II)] chloride 
• 2071-20-7 bis-diphenylphosphinomethane 
• 12080-32-9 dichloro(1,5-cyclooctadiene)platinum(ll) 
• 63911-00-2 {PtH2(μ-H)(μ-dppm)2}PF6 
• 14221-02-4 tetrakis(triphenylphosphine)platinum 
• 14873-92-8 dichlorobis(diethyl sulfide)platinum 

Downstream Products

• 123676-63-1 {Pt(bis(diphenylphosphino)methane)(BH₂(CN)2)}2 
• 114692-91-0 {Pt₂(dppm)2(CH₃CN)2}(BF₄)2 
• 68851-48-9 Pt₂Cl₂(S)(CH₂(P(C₆H₅)2)2)2 
• 124294-98-0 C₅₂H₄₇ClNP₄Pt₂⁽¹⁺⁾ 
• 123676-62-0 {Pt(bis(diphenylphosphino)methane)(BH₃CN)}2 
• 68851-49-0 Pt₂Cl₂CH₂((C₆H₅)4P₂CH₂)2 
• 124294-99-1 Pt₂Cl(CH₃CN)((C₆H₅)2PCH₂P(C₆H₅)2)2⁽¹⁺⁾*BF₄^(1-)={Pt₂Cl(CH₃CN)((C₆H₅)2PCH₂P(C₆H₅)2)2}BF₄ 
• 124272-67-9 Pt₂Cl(ONO₂)((C₆H₅)2PCH₂P(C₆H₅)2)2 
• 106193-58-2 {Pt2Cl2(μ-AuCl)(μ-dppm)2} 

Relevant academic research and scientific papers

A route to trinuclear platinum-gold clusters

New A-frame cluster complexes have been prepared by addition of electrophilic gold fragments to the Pt-Pt bond of , dppm = Ph2PCH2PPh2.For example, gave and gave NO3.The complexes reacted with to give BF4 when n = 1 or 2, but the bridged bis(A-frame) cluster complex 2CH2>(BF4)2 when n = 3.In contrast, CuCl reacted with to give .Attempts to synthesize A-frame clusters containing Pt2Ag, Pt2Cu, Pd2Au, or PdPtAu units were unsuccessful, and it is concluded that these units are considerably weaker than the analogous 3-center 2-electron bond of the Pt2Au unit.The AuCl unit is displaced from on reaction with diazomethane, with formation of .Key words: platinum, gold, cluster, copper, silver.

Ligand substitution reactions of a dinuclear platinum (I) complex

The complex Pt2Br2(μ-dppm)2 reacts with Et4NCl in dichloromethane and dichloroethane to form Pt2Cl2(μ-dppm)2. The reaction is reversible and proceeds via stepwise formation of the mixed-ligand (Br, Cl) complex. The reaction follows biphasic kinetics, and each step shows a linear dependence on [Et4NCl], with rate constants 93 ± 20 and 19.4 ± 1.2 M-1 s-1 for the respective steps (10.0°C in CH2Cl2). The identification of a rate constant with an individual step is a process that inherently admits of dual solutions; the assignment of k1 = 93 M-1 s-1 and k2 = 19.4 M-1 s-1 was made on the basis that only this model gave a consistent and reasonable value for the molar absorptivity of the mixed-halide intermediate. The reaction in 1,2-dichloroethane shows a quite different kinetic pattern, with a single pseudo-first-order rate law and a more complex variation of kobsd with [Et4NCl].

Binuclear reductive elimination reactions in diplatinum complexes: Synthesis of hydridoplatinum(I) complexes

The complex [Pt2H2(μ-H)(μ-dppm)2][PF6] (1) (dppm = Ph2PCH2PPh2) reacts with tertiary phosphine ligands to give H2 and the hydridoplatinum(I) complexes [Pt2HL(μ-dppm)2][PF6] (4, L = η1-dppm; 5, L = PMe2Ph; 6, L = PMePh2; 7, L = PPh3). Complex 4 is also obtained by the reduction of [Pt(dppm)2][PF6]2 with sodium borohydride. Study of the 1H and 31P NMR spectra of 4-7 is in accord with the presence of Pt-Pt bonds and, in the case of 4, shows that its structure in solution is similar to that previously determined in the solid state by an X-ray investigation. Methanethiol reacts reversibly with 4 to give [Pt2H2(μ-SMe)(μ-dppm)2][PF6]. Attempts to prepare diplatinum(0) complexes by deprotonation of 4 or 7 were unsuccessful.