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      Further studies on the dialkylation chemistry of [Pt₂(μ-S)₂(PPh₃)₄] with activated alkyl halides RC(O)CH₂X (X = Cl, Br)

      Ujam, Oguejiofo Theophilus; Henderson, William; Nicholson, Brian K.; Hor, T.S. Andy
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      DOI
       10.1016/j.ica.2011.06.023
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       www.sciencedirect.com
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      Ujam, O.T., Henderson, W., Nicholson, B.K. & Hor, T.S.A. (2011). Further studies on the dialkylation chemistry of [Pt₂(μ-S)₂(PPh₃)₄] with activated alkyl halides RC(O)CH₂X (X = Cl, Br). Inorganica Chimica Acta, available online 21 June 2011.
      Permanent Research Commons link: https://hdl.handle.net/10289/5455
      Abstract
      Further studies have been carried out into the reactivity of [Pt₂(μ-S)₂(PPh₃)₄] towards a range of activated alkylating agents of the type RC(O)CH₂X (R = organic moiety e.g. phenyl, pyrenyl; X = Cl, Br). Alkylation of both sulfide centres is observed for PhC(O)CH₂Br, 3-(bromoacetyl)coumarin [CouC(O)CH₂Br], and 1-(bromoacetyl)pyrene [PyrC(O)CH2Br], giving dications [Pt₂{μ-SCH₂C(O)R}₂ (PPh₃)₄] ²⁺, isolated as their PF₆⁻ salts. The X-ray structure of [Pt₂{μ-SCH₂C(O)Ph}₂ (PPh₃)₄](PF₆) ₂ shows the presence of short Pt•••O contacts. In contrast, the corresponding chloro compounds [typified by PhC(O)CH₂Cl] and imino analogues [e.g. PhC(NOH)CH₂Br] do not dialkylate [Pt₂ (μ-S)₂(PPh₃)₄]. The ability of PhC(O)CH₂Br to dialkylate [Pt₂(μ-S)₂(PPh₃)₄] allows the synthesis of new mixed-alkyl dithiolate derivatives of the type [Pt₂{μ-SCH₂C(O)Ph}(μ-SR)(PPh₃)₄]²⁺ (R = Et or n-Bu), through alkylation of in situ-generated monoalkylated compounds [Pt₂(μ-S)(μ-SR)(PPh₃)₄]⁺ (from [Pt₂(μ-S)₂(PPh₃)₄] and excess RBr). In these heterodialkylated systems ligand replacement of PPh₃ occurs by the bromide ions in the reaction mixture forming monocations [Pt₂{μ-SCH₂C(O)Ph}(μ-SR)(PPh₃)₃Br]⁺. This ligand substitution can be easily suppressed by addition of PPh₃ to the reaction mixture. The complex [Pt₂{μ-SCH₂C(O)Ph}(μ-SBu)(PPh₃)₄]²⁺ was crystallographically characterised. X-ray crystal structures of the bromide-containing complexes [Pt₂{μ-SCH₂C(O)Ph}(μ-SR)(PPh₃)₃Br]+ (R = Et, Bu) are also reported. In both structures the coordinated bromide is trans to the SCH₂C(O)Ph ligand, which adopts an axial position, while the ethyl and butyl substituents adopt equatorial positions, in contrast to the structures of the dialkylated complexes [Pt₂{μ-SCH₂C(O)Ph}₂(PPh₃)₄]²⁺ and [Pt₂{μ-SCH₂C(O)Ph}(μ-SBu)(PPh₃)₄]²⁺ (and many other known analogues) where both alkyl groups adopt axial positions.
      Date
      2011
      Type
      Journal Article
      Publisher
      Elsevier BV
      Rights
      This is an author’s accepted version of an article published in the journal: Inorganica Chimica Acta. © 2011 Elsevier.
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      • Science and Engineering Papers [3084]
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