10569-17-2

Basic information

• Product Name: Phosphine, tris(trimethylstannyl)-
• CAS NO: 10569-17-2
• Molecular Formula: C9H27PSn3
• Molecular Weight: 522.417
• Mol File: 10569-17-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Phosphine, tris(trimethylstannyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphine, tris(trimethylstannyl)-(10569-17-2)
• EPA Substance Registry System: Phosphine, tris(trimethylstannyl)-(10569-17-2)

Safety Data

• Hazardous Substances Data: 10569-17-2(Hazardous Substances Data)

Upstream product

• 1066-45-1 trimethyltin(IV)chloride 

Downstream Products

• 180737-43-3 (2,4,6-trimethylphenyl)SiCl₂P(Sn(CH₃)3)2 
• 180737-44-4 (2,4,6-triisopropylphenyl)SiCl₂P(Sn(CH₃)3)2 
• 176036-49-0 bis(trimethylstannyl)phosphino-di-tert-butylcyclotriphosphane 
• 1066-45-1 trimethyltin(IV)chloride 
• 670237-49-7 tetrastannylphosphonium pentafluorosilicate 
• 671222-97-2 [bis(2,4,6-triisopropylphenyl)SnPH]2 
• 314241-34-4 tetrakis(trimethylstannyl)phosphonium BPh₄ 
• 16010-26-7 (CO)3NiP(Sn(CH₃)3)3 
• 7803-51-2 phosphan 
• 40392-56-1 Trimethylstannyl-trifluormethyl-phosphin 
• 40392-60-7 Bis-(trimethylstannyl)-trifluormethyl-phosphin 

Relevant articles and documents

Reactions of Imidazolio-Phosphides with Organotin Chlorides: Surprisingly Diverse

Reactions of primary imidazolio-phosphides (“imidazolylidene-phosphinidenes”) with R2SnCl2 yield as main products spectroscopically detectable Lewis pairs which undergo base-induced dehydrochlorination in the presence of excess dichlorostannane to afford zwitterionic chloride adducts of distannylated imidazolio-phosphines. In contrast, reactions with R3SnCl proceed under dismutation to furnish mixtures containing imidazolium salts and stannylated (oligo)phosphines P(SnR3)3 and P7(SnR3)3, respectively. DFT studies were used to rationalize the divergent behavior based on the presumption that the reactions proceed under thermodynamic control and the products observed represent the most stable species under the specific reaction conditions. Computational simulation of selected reaction steps provides a model mechanism for Lewis-acid promoted creation of PP-bonds, which is a prerequisite for oligophosphine formation. The computational studies further highlight parallels between reactions of imidazolio-phosphides with Lewis and Br?nsted acids, and allow also to extrapolate the behavior of the P-nucleophiles towards other electrophiles than organotin chlorides.