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      The crystal structures and Hirshfeld surface analyses of a cadmium(II) and a zinc(II) mononuclear complex of the new tetrakis-substituted pyrazine ligand N, N′, N′′, N′′′-[pyrazine-2,3,5,6-tetra­yltetra­kis­(methyl­ene)]tetra­kis­( N-methyl­aniline)

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          Abstract

          In the cadmium(II) and zinc(II) complexes of the tetra­kis-substituted pyrazine ligand, N, N′, N′′, N′′′-[pyrazine-2,3,5,6-tetra­yltetra­kis­(methyl­ene)]tetra­kis­( N-methyl­aniline), the ligand coordinates in a mono-tridentate fashion, and both metal atoms have fivefold coordination spheres with distorted shapes.

          Abstract

          The whole mol­ecule of the cadmium(II) complex, di­iodido­{ N, N′, N′′, N′′′-[pyrazine-2,3,5,6-tetra­yltetra­kis­(methyl­ene)]tetra­kis­( N-methyl­aniline)-κ 3 N 2, N 1, N 6}cadmium(II), [CdI 2(C 36H 40N 6)], ( I), of the ligand N, N′, N′′, N′′′-[pyrazine-2,3,5,6-tetra­yltetra­kis­(methyl­ene)]tetra­kis­( N-methyl­aniline) ( L), is generated by a twofold rotation symmetry; the twofold axis bis­ects the cadmium atom and the nitro­gen atoms of the pyrazine ring. The ligand coordinates in a mono-tridentate manner and the cadmium atom has a fivefold CdN 3I 2 coordination environment with a distorted shape. In the zinc(II) complex, dichlorido{ N, N′, N′′, N′′′-[pyrazine-2,3,5,6-tetra­yltetra­kis­(methyl­ene)]tetra­kis­( N-methyl­aniline)-κ 3 N 2, N 1, N 6}zinc(II) di­chloro­methane 0.6-solvate, [ZnCl 2(C 36H 40N 6)]·0.6CH 2Cl 2, ( II), ligand L also coordinates in a mono-tridentate manner and the zinc atom has a fivefold ZnN 3Cl 2 coordination environment with a distorted shape. It crystallized as a partial di­chloro­methane solvate. In the crystal of I, the complex mol­ecules are linked by weak C—H⋯I contacts, forming ribbons propagating along [100]. In the crystal of II, the complex mol­ecules are linked by a series of C—H⋯π inter­actions, forming layers lying parallel to the (1 1) plane. In the crystals of both compounds there are metal–halide⋯π(pyrazine) contacts present. The Hirshfeld analyses confirm the importance of the C—H⋯halide contacts in the crystal packing of both compounds.

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          Author and article information

          Journal
          Acta Crystallogr E Crystallogr Commun
          Acta Crystallogr E Crystallogr Commun
          Acta Cryst. E
          Acta Crystallographica Section E: Crystallographic Communications
          International Union of Crystallography
          2056-9890
          01 March 2020
          18 February 2020
          18 February 2020
          : 76
          : Pt 3 ( publisher-idID: e200300 )
          : 410-416
          Affiliations
          [a ]Institute of Chemistry, University of Neuchâtel , Av. de Bellevaux 51, CH-2000 Neuchâtel, Switzerland
          [b ]Institute of Physics, University of Neuchâtel , rue Emile-Argand 11, CH-2000 Neuchâtel, Switzerland
          Author notes
          Article
          xi2022 ACSECI S2056989020001644
          10.1107/S2056989020001644
          7057360
          2ded44a6-0196-4b4e-bf35-5446db396b4a
          © Tesouro Vallina and Stoeckli-Evans 2020

          This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

          History
          : 24 January 2020
          : 05 February 2020
          Page count
          Pages: 7
          Funding
          Funded by: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
          Funded by: University of Neuchâtel
          This work was funded by Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung grant . University of Neuchâtel grant .
          Categories
          Research Communications

          crystal structure,tetra­kis-substituted pyrazine,cadmium(ii),zinc(ii),mononuclear complexes,c—h⋯π inter­actions,metal–halide⋯π(pyrazine) contacts

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