A cooperative pathway for water activation using a bimetallic Pt0-CuI system. Academic Article uri icon


  • A mixture of the platinum(0) complex [Pt(PtBu3)2] and tetrakis(acetonitrile)copper(i) hexafluorophosphate in acetone activated a water molecule and gave the hydride platinum(ii) complex [PtH(CH3CN)(PtBu3)2]PF6, 1, and the hydroxide Cu(i) species. The crystal structure of complex 1 was determined by X-ray crystallography, indicating a distorted square planar geometry around the platinum center. Although three possible mechanisms are proposed for this transformation, monitoring of the reaction using NMR spectroscopy at low temperature reveals that a cooperative pathway involving formation of a Pt0-CuI dative bond complex is the most probable pathway. The hydride platinum complex 1 is stable in acidic and neutral conditions but undergoes intramolecular C-H activation in the presence of pyridine. Monitoring of the reaction using 1H and 31P NMR spectroscopy shows that a cyclometalation reaction of one of the phosphine ligands is followed by displacement of a second phosphine ligand by pyridine to give the cyclometalated platinum(ii) complex, [Pt(2PC-PtBu2CMe2CH2)(py)2], 4. The structure of 4 in solution and solid state phases was determined using NMR spectroscopy and X-ray crystallography, respectively.

published proceedings

  • Dalton Trans

altmetric score

  • 9.25

author list (cited authors)

  • Jamali, S., Abedanzadeh, S., Khaledi, N. K., Samouei, H., Hendi, Z., Zacchini, S., Kia, R., & Shahsavari, H. R.

citation count

  • 14

complete list of authors

  • Jamali, S||Abedanzadeh, S||Khaledi, NK||Samouei, H||Hendi, Z||Zacchini, S||Kia, R||Shahsavari, HR

publication date

  • November 2016