Abstract

The asymmetric unit of the title compound, catena-poly[[[(1,4,8,11-tetra-aza-cyclo-tetra-decane-κ4 N 1,N 4,N 8,N 11)nickel(II)]-μ-cyanido-κ2 N:C-[bis-(cyanido-κC)nickel(II)]-μ-cyanido-κ2 C:N] dihydrate], {[Ni2(CN)4(C10H24N4)]·2H2O] n or [{[Ni(C10H24N4)][Ni(CN)4]}·2H2O] n , consists of a pair of crystallographically non-equivalent macrocyclic cations and anions. The nickel(II) ions (all with site symmetry ) are coordinated by the four secondary N atoms of the macrocyclic ligands, which adopt the most energetically stable trans-III conformation, and the mutually trans N atoms of the tetra-cyano-nickelate anion in a slightly tetra-gonally distorted NiN6 octa-hedral coordination geometry. The [Ni(CN)4)]2- anion exhibits a bridging function, resulting in the formation of parallel polymeric chains running along the [10] direction. The water mol-ecules of crystallization play a pivotal role in the three-dimensional supra-molecular organization of the crystal. Acting as acceptors, they form N-H⋯Ow (w = water) hydrogen bonds with the secondary amino groups of the macrocycles, forming layers oriented parallel to the (001) plane. At the same time, as donors, they inter-act with the non-coordinated cyano groups of the anion via Ow-H⋯Nc (c = cyanide) hydrogen bonds, giving two-dimensional layers oriented parallel to the (100) plane and thus generating a three-dimensional network.

Highlights

  • The asymmetric unit of the title compound, catena-poly[[[(1,4,8,11-tetraazacyclotetradecane-4N1,N4,N8,N11)nickel(II)]--cyanido-2N:C-[bis(cyanidoC)nickel(II)]--cyanido-2C:N] dihydrate], {[Ni2(CN)4(C10H24N4)]Á2H2O]n or [{[Ni(C10H24N4)][Ni(CN)4]}Á2H2O]n, consists of a pair of crystallographically non-equivalent macrocyclic cations and anions

  • The [Ni(CN)4)]2– anion exhibits a bridging function, resulting in the formation of parallel polymeric chains running along the [110] direction

  • The tetracyanonickelate(II) dianion has attracted less attention compared to hexa- and octacyanometallates and only one work describing the structure of the coordination polymer formed by the metal(cyclam) complex and this anion, i.e., {Cu(L)[Ni(CN)4]}n, has been published to date (Cernak et al, 2010)

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Summary

Chemical context

Transition-metal complexes of tetraazamacrocyclic ligands, in particular of 1,4,8,11-tetraazacyclotetradecane (cyclam, L), have been intensively studied for decades This is explained by their unique properties, in particular, exceptionally high thermodynamic stability, kinetic inertness and the ability to stabilize uncommon oxidation states of coordinated metals (Melson, 1979; Yatsimirskii & Lampeka, 1985). Because of their conformational rigidity during chemical transformation (preservation of two vacant or labile trans axial positions in the coordination sphere of the metal ion), these complexes are promising secondary building units for the construction of metal–organic frameworks (MOFs) (Lampeka & Tsymbal, 2004; Suh & Moon, 2007; Suh et al, 2012; Stackhouse & Ma, 2018), which possess great potential for applications in different areas including gas storage, separation, catalysis, sensing, etc (MacGillivray & Lukehart, 2014; Kaskel, 2016). We report the synthesis and crystal structure of the coordination polymer built up of the nickel(II) complex of L and the tetracyanonickelate(II) dianion, namely, catena-[bis(2-cyano-2C,N)-dicyano-(1,4,8,11-tetraazacyclotetradecane-4N1,N4,N8,N11)-dinickel(II) dihydrate], [{[Ni(L)][Ni(CN)4]}Á2H2O]n, (I)

Structural commentary
Supramolecular features
Database survey
Synthesis and crystallization
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