Reactivity of [Pt2(μ-S)2(PPh3)4] towards activated aliphatic bromoacyl electrophiles: Formation of mono-, homodi-, heterodi- and intramolecular-bridged alkylated products

The reactivity of the metalloligand Pt2(μ-S)2(PPh3)4 with the boron-functionalized alkylating agents BrCH2(C6H4)B(OR)2 (R = H or CMe2) was investigated by electrospray ionization mass spectrometry (ESI-MS) in real time using the pressurized sample infusion (PSI). The macroscopic reaction of Pt2(μ-S)2(PPh3)4 with one mole equivalent of alkylating agents BrCH2(C6H4)B{OC(CH3)2}2 and BrCH2(C6H4)B(OH)2 gave the dinuclear monocationic µ-sulfide thiolate complexes [Pt2(µ-S){µ-SCH2(C6H4)B{OC(CH3)2}2} (PPh3)

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Alkylation of [Pt₂(μ-S)₂(PPh₃)₄] with boronic acid derivatives

Ujam

Offie

Ukoha

et al. 2016

Journal of Coordination Chemistry

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Reactivity of [Pt2(μ-S)2(PPh3)4] towards activated aliphatic bromoacyl electrophiles: Formation of mono-, homodi-, heterodi- and intramolecular-bridged alkylated products

Cited by 1 publication

References 35 publications

Alkylation of [Pt₂(μ-S)₂(PPh₃)₄] with boronic acid derivatives

Alkylation of [Pt₂(μ-S)₂(PPh₃)₄] with boronic acid derivatives

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Reactivity of [Pt2(μ-S)2(PPh3)4] towards activated aliphatic bromoacyl electrophiles: Formation of mono-, homodi-, heterodi- and intramolecular-bridged alkylated products

Cited by 1 publication

References 35 publications

Alkylation of [Pt2(μ-S)2(PPh3)4] with boronic acid derivatives

Alkylation of [Pt2(μ-S)2(PPh3)4] with boronic acid derivatives

Contact Info

Product

Resources

About

Alkylation of [Pt₂(μ-S)₂(PPh₃)₄] with boronic acid derivatives

Alkylation of [Pt₂(μ-S)₂(PPh₃)₄] with boronic acid derivatives