Tetrametallic [2 x 1+1 x 2], octametallic double-decker-triple-decker [5 x 1+3 x 1], hexametallic quadruple-decker and dimetallic-based one-dimensional complexes of copper(II) and s block metal ions derived from N,N '-ethylenebis(3-ethoxysalicylaldimine)

Sujit Sasmal, Samit Majumder, Susanta Hazra, Hazel A. Sparkes, Judith A. K. Howard, Malabika Nayak, Sasankasekhar Mohanta*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)

45 Citations (Scopus)

Abstract

In the present investigation, various copper(II)-alkali/alkaline earth metal ion heteronuclear complexes derived from N,N'-ethylenebis(3-ethoxysalicylaldimine) (H2L) have been studied. The syntheses, characterization and crystal structures of three [2 x 1 + 1 x 2] cocrystals [{(CuLLiI)-L-II(H2O)(2)}{(CuL)-L-II}(2)](ClO4) (1), [{(CuLNaI)-L-II(H2O)(2)}{(CuL)-L-II}(2)](dicyanamide) (2) and [{(CuLMgII)-L-II(H2O)(3)}{(CuL)-L-II}(2)](NO3)(2)center dot H2O (3), one [3 x 1 + 5 x 1] double-decker-triple-decker cocrystal [{((CuL)-L-II)(2)K-I}(ClO4)]center dot[{((CuL)-L-II)(3)K-2(I)(mu-ClO4)}(ClO4)] (4), one dinuclear (CuKI)-K-II-based one-dimensional polymer [(CuLKI)-L-II(mu-PF6)](n) (5) and one hexametallic quadruple-decker compound [{((CuL)-L-II)(2)Rb-I(mu-H2O)}(2)](BPh4)(2)center dot 2CH(3)COCH(3) (6) are reported. Compounds 1, 2, 3 and 6 crystallize in the triclinic crystal system (space group P (1) over bar), while the crystal systems of 4 and 5 are monoclinic (space group C2/c) and orthorhombic (space group P2(1)2(1)2(1)), respectively. The cocrystallization in 1-3 takes place through the encapsulation of coordinated water molecules into the O-4 compartment of two mononuclear [(CuL)-L-II] moieties; both the coordinated water molecules are involved in the case of 1 and 2, while 2 of the 3 coordinated water molecules are involved for 3. In 4, the potassium(I) centre in the double-decker moiety is sandwiched in between two mononuclear [(CuL)-L-II] moieties, while each of the two potassium(I) centres in the triple-decker moiety are sandwiched in between a pair of two [(CuL)-L-II] moieties. The two potassium(I) centres in the triple-decker moiety are bridged by a perchlorate anion. In 5, two cis fluorine atoms from the hexafluorophosphate anion bridge the potassium(I) centres of the neighbouring dinuclear (CuKI)-K-II units to build up a one-dimensional polymer. The quadruple-decker hexanuclear [{((CuL)-L-II)(2)Rb-I(mu-H2O)}(2)](2+) dication in 6 can be considered to consist of two trinuclear double-decker [((CuL)-L-II)(2)Rb-I](+) moieties, interlinked by two bridging water molecules. Structural resemblance between the structures formed with Li-I, Na-I and Mg-II and those with 3d metal ions, the anion dependence of the topology of the copper(II)-potassium(I) complexes, cocrystallization in the presence of the potentially bridging dicyanamide anion, the first report of a one-dimensional polymer derived from H2L and an interesting example of a quadruple-decker complex, are the major outcomes of the present investigation. All in all, structural diversity in the H2L ligand system has been further enriched by some interesting structures in the present investigation.

Original languageEnglish
Pages (from-to)4131-4140
Number of pages10
JournalCrystEngComm
Volume12
Issue number12
DOIs
Publication statusPublished - 2010

Keywords

  • MAGNETIC-PROPERTIES
  • MONONUCLEAR
  • DINUCLEAR
  • FERROCENE
  • SANDWICH
  • BENZENE
  • CATION
  • LI+
  • CU

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