JOURNAL ARTICLE

[(C6H10)(NH3)2][Ni(H2O)4C6H2(COO)4]·4H2O – A Coordination Polymer with the Chain‐like Polyanion {Ni(H2O)4[C6H2(COO)4]2−}n

Roberto KöfersteinChristian Robl

Year: 2007 Journal:   Zeitschrift für anorganische und allgemeine Chemie Vol: 633 (9)Pages: 1323-1325   Publisher: Wiley

Abstract

Abstract Triclinic single crystals of [(C 6 H 10 )(NH 3 ) 2 ][Ni(H 2 O) 4 C 6 H 2 (COO) 4 ]·4H 2 O have been prepared in aqueous solution at 55 °C. Space group (Nr. 2), a = 691.23(6), b = 924.84(5), c = 1082.43(7) pm, α = 74.208(6)°, β = 75.558(7)°, γ = 68.251(6)°, V = 0.60985(7) nm 3 , Z = 1. The Nickel(II) species, located on a crystallographic inversion centre, is coordinated in a trans‐ octahedral fashion by two oxygen atoms stemming from the centrosymmetric pyromellitate anions and four from water molecules (Ni–O 205.82(12) – 208.11(13) pm). The connection between Ni 2+ and [C 6 H 2 (COO) 4 )] 4− leads to infinite chain‐like polyanions extending parallel to with {Ni(H 2 O) 4 [C 6 H 2 (COO) 4 ] 2− } n composition. [(C 6 H 10 )(NH 3 ) 2 ] 2+ ‐cations are accomodated between the chains, compensating for the negative charge of the polyanions. Thermogravimetric analysis in air showed that the loss of water of crystallisation occurs in two steps between 102 and 206 °C, corresponding to the loss of 6 and 2 water molecules per formula unit, respectively. The dehydrated sample was stable between 206 and 353 °C. Further decomposition yielded nickel(II) oxide (NiO).

Keywords:
Triclinic crystal system Crystallography Octahedron Nickel Aqueous solution Chemistry Non-blocking I/O Molecule Formula unit Thermogravimetric analysis Thermal decomposition Crystal structure Physical chemistry

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Topics

Metal-Organic Frameworks: Synthesis and Applications
Physical Sciences →  Chemistry →  Inorganic Chemistry
Polyoxometalates: Synthesis and Applications
Physical Sciences →  Materials Science →  Materials Chemistry
Magnetism in coordination complexes
Physical Sciences →  Materials Science →  Electronic, Optical and Magnetic Materials

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