Molecules (Feb 2023)

Study of the Counter Cation Effects on the Supramolecular Structure and Electronic Properties of a Dianionic Oxamate-Based {Ni<sup>II</sup><sub>2</sub>} Helicate

  • Cintia A. Simosono,
  • Rafaela M. R. da Silva,
  • Nathália R. De Campos,
  • Marye Agnes R. Silva,
  • Antônio C. Doriguetto,
  • Leonã S. Flores,
  • Charlane C. Correa,
  • Tatiana R. G. Simões,
  • Ana Karoline S. M. Valdo,
  • Felipe T. Martins,
  • Flávio Garcia,
  • Guilherme P. Guedes,
  • Breno R. L. Galvão,
  • Juliana Cancino-Bernardi,
  • Ricardo D. dos Reis,
  • Humberto O. Stumpf,
  • Danielle D. Justino,
  • Paulo F. R. Ortega,
  • Walace D. do Pim,
  • Miguel Julve,
  • Maria Vanda Marinho

DOI
https://doi.org/10.3390/molecules28052086
Journal volume & issue
Vol. 28, no. 5
p. 2086

Abstract

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Herein, we describe the synthesis, crystal structure, and electronic properties of {[K2(dmso)(H2O)5][Ni2(H2mpba)3]·dmso·2H2O}n (1) and [Ni(H2O)6][Ni2(H2mpba)3]·3CH3OH·4H2O (2) [dmso = dimethyl sulfoxide; CH3OH = methanol; and H4mpba = 1,3-phenylenebis(oxamic acid)] bearing the [Ni2(H2mpba)3]2− helicate, hereafter referred to as {NiII2}. SHAPE software calculations indicate that the coordination geometry of all the NiII atoms in 1 and 2 is a distorted octahedron (Oh) whereas the coordination environments for K1 and K2 atoms in 1 are Snub disphenoid J84 (D2d) and distorted octahedron (Oh), respectively. The {NiII2} helicate in 1 is connected by K+ counter cations yielding a 2D coordination network with sql topology. In contrast to 1, the electroneutrality of the triple-stranded [Ni2(H2mpba)3] 2− dinuclear motif in 2 is achieved by a [Ni(H2O)6]2+ complex cation, where the three neighboring {NiII2} units interact in a supramolecular fashion through four R22(10) homosynthons yielding a 2D array. Voltammetric measurements reveal that both compounds are redox active (with the NiII/NiI pair being mediated by OH– ions) but with differences in formal potentials that reflect changes in the energy levels of molecular orbitals. The NiII ions from the helicate and the counter-ion (complex cation) in 2 can be reversibly reduced, resulting in the highest faradaic current intensities. The redox reactions in 1 also occur in an alkaline medium but at higher formal potentials. The connection of the helicate with the K+ counter cation has an impact on the energy levels of the molecular orbitals; this experimental behavior was further supported by X-ray absorption near-edge spectroscopy (XANES) experiments and computational calculations.

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