Covalent Co–O–V and Sb–N Bonds Enable Polyoxovanadate Charge Control

نویسندگان

  • Maren Rasmussen
  • Christian Näther
  • Jan van Leusen
  • Paul Kögerler
  • Lyuben Zhechkov
  • Thoma Heine
  • Wolfgang Bensch
چکیده

The formation of [{CoII(teta)2}{CoII2(tren)(teta)2}VIV15SbIII6O42(H2O)]·ca.9H2O [teta = triethylenetetraamine; tren = tris(2-aminoethyl)amine] illustrates a strategy toward reducing the molecular charge of polyoxovanadates, a key challenge in their use as components in single-molecule electronics. Here, a V-O-Co bond to a binuclear Co2+-centered complex and a Sb-N bond to the terminal N atom of a teta ligand of a mononuclear Co2+ complex allow for full charge compensation of the archetypal molecular magnet [V15Sb6O42(H2O)]6-. Density functional theory based electron localization function analysis demonstrates that the Sb-N bond has an electron density similar to that of a Sb-O bond. Magnetic exchange coupling between the VIV and CoII spin centers mediated via the Sb-N bridge is comparably weakly antiferromagnetic.

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عنوان ژورنال:

دوره 56  شماره 

صفحات  -

تاریخ انتشار 2017