60751-01-1

Upstream product

• 66485-00-5 PtMe(4-MeC₆H₄)(1,5-cyclooctadiene) 
• 41119-53-3 ((CH₃)2(C₆H₅)P)2PtI₂ 
• 12266-72-7 (1,5-cylooctadiene)di-iodoplatinum(II) 
• 937-12-2 4-tolyltrimethylstannane 
• 66485-01-6 Au(C₆H₄(CH₃))(CH₃)2(P(C₆H₅)3) 

Downstream Products

• 66485-00-5 PtMe(4-MeC₆H₄)(1,5-cyclooctadiene) 

Relevant academic research and scientific papers

Selectivity in reactions of alkyl-aryl-transition-metal complexes with electrophiles

The new methylarylmetal complexes cis-[AuMe2Ph(PPh3)], cis-[AuMe2(4-MeC6H4)(PPh3)], [PtMe(4-MeC6H4)(C8H12)], cis-[PtMePh(PMePh2)2], and cis-[PtMe(4-MeC6H4)(PMe2Ph)2] have been prepared and characterized. In reactions with electrophilic reagents such as HCl, HgCl2, and [PtI2(PMe2Ph)2], the complexes undergo selective cleavage of a methyl-metal bond (e.g., cis-[PtMePh(PMePh2)2]) or an aryl-metal bond (e.g., cis-[AuMe2Ph(PPh3)], [PtMe(4-MeC6H4)(C8H12)]). From the selectivity observed and from studies of relative rates of reaction, it is argued that the SE2 mechanism leads to selective aryl-metal bond cleavage and that a different mechanism, probably involving an oxidative-addition-reductive-elimination sequence, leads to selective methyl-metal bond cleavage.