JOURNAL OF CHILEAN CHEMICAL SOCIETY

Vol 64 No 2 (2019): Journal of the Chilean Chemical Society
Original Research Papers

µ-BENZENE-1,2,4,5-TETRACARBOXYLATO-κ2O1:O4)BIS[ AQUABIS- 2-(AMINOMETHYL) PYRIDINE-κ2N,N') NICKEL (II)] DECAHYDRATE: STRUCTURE AND MAGNETIC PROPERTIES

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  • Ana María Atria,
  • José Parada,
  • Ricardo Baggio,
  • Octavio Peña,
  • Yanko Moreno
Ana María Atria
Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile
José Parada
Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile
Ricardo Baggio
Gerencia de Investigación y Aplicaciones, Centro Atómico Constituyentes, Comisión Nacional de Energía Atómica
Octavio Peña
Univ Rennes, CNRS, ISCR [ ( Institut des Sciences Chimiques de Rennes)]
Yanko Moreno
Universidad Andres Bello, Departamento de Ciencias Químicas, Facultad de Ciencias Exactas
Published July 25, 2019
Keywords
  • crystal structure,
  • nickel complex,
  • magnetism
How to Cite
Atria, A. M., Parada, J., Baggio, R., Peña, O., & Moreno, Y. (2019). µ-BENZENE-1,2,4,5-TETRACARBOXYLATO-κ2O1:O4)BIS[ AQUABIS- 2-(AMINOMETHYL) PYRIDINE-κ2N,N’) NICKEL (II)] DECAHYDRATE: STRUCTURE AND MAGNETIC PROPERTIES. Journal of the Chilean Chemical Society, 64(2). Retrieved from https://jcchems.com/index.php/JCCHEMS/article/view/1218

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Abstract

µ-Benzene-1,2,4,5-tetracarboxylato-κ2O1:O4)bis[aquabis-2-(aminomethyl) pyridine-κ2N,N') nickel (II)] decahydrate, [Ni2(amp)4(btc)(H2O)2].10H2O has been synthesized and its crystal structure determined by X-ray diffraction. The complex crystallizes in the Monoclinic space group P21/n with cell dimensions a= 11.0102 (10) Å, b= 21.5416 (19) Å, c= 11.0445 (10) Å and ß= 118.753 (1)°, and two formula units per cell (Z= 2, Z’= 0.5).

The structure consists of centrosymmetric dimeric units in which the benzene tetracarboxylate anions (btc) bridge the symmetry–related nickel (II) cations, two bidentate chelating molecules of 2-(aminomethyl) pyridine and a terminal aqua ligand completing the six-fold coordination at each metal. These dimers link to each other via H-bonding to form chains parallel to [100], while the water solvates form a strongly bound 2D network parallel to (100), made up by small (R44(8) ) and large (R20 20(40)) rings, the latter ones “pierced” by the chains of dimmers, with a profuse H-bonding interconnection between both substructures.

Magnetic susceptibility measurements as a function of temperature disclose weak interdimeric exchange interactions. Fitting of these data to a dimeric model yields J= -3.5 cm-1 and g= 2.13.

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