From discrete molecules to one-dimensional coordination polymers containing Mn(II), Zn(II) or Cd(II) pyridine-2-aldoxime building unit

    Authors

    L. Croitor; E. B. Coropceanu; A. V. Siminel; A. E. Masunov;M. S. Fonari

    Comments

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    Abbreviated Journal Title

    Polyhedron

    Keywords

    Coordination polymers; Pyridine-2-aldoxime; X-ray; Fluorescence; properties; MANGANESE CARBOXYLATE CHEMISTRY; ORGANIC FRAMEWORK MATERIALS; 2-PYRIDYL; KETONE OXIME; CRYSTAL-STRUCTURE; PARTIAL TRANSFORMATION; LUMINESCENT; PROPERTIES; X-RAY; COMPLEXES; MONONUCLEAR; TETRANUCLEAR; Chemistry, Inorganic & Nuclear; Crystallography

    Abstract

    The syntheses, spectroscopic characterization and crystal structures for eight coordination compounds [Cd(HCO2)(2)(pya)(2)] (1), {[M(bdc)(pya)]center dot 1.5DMF}(n) (M = Mn(II), Zn(II), Cd(II) (2-4), [Zn(SO4)(Pya)(H2O)(3)] (H2O) (5), [(ZnSO4)(2)(pya)(4)] DMF center dot 2H(2)O (6), [Zn(SO4)(pya(H2O)(2)](n) (7), and [Cd(SO4)(pya)(H2O)](n) (8) [pya = pyridine-2-aldoxime, bdc = 1,4-benzenedicarboxylate, DMF = N,N'-dimethylformamide] are reported. Compounds 1-4 and 6 contain two, while 5, 7, and 8 contain one neutral pya ligand coordinated in a chelate mode to the metal center through the N-pyridyl and N-oxime atoms. The dicarboxylic bdc anions provide an access to 1D polymeric arrays in 2-4. The hybrid sulfates including discrete mononuclear (5), binuclear (6), and 1D polymeric (7, 8) coordination arrays were obtained due to different binding modes of coordinated sulfate anion. While solid state fluorescence of new polymeric compounds 2-4 is similar to that of the H(2)bdc ligand, a rare dual emission is observed for compounds 7 and 8. According to TD-DFT calculations, emission at 400 and 650 nm originates from n pi* and pi pi* states of the pya ligand respectively. (C) 2013 Elsevier Ltd. All rights reserved.

    Journal Title

    Polyhedron

    Volume

    60

    Publication Date

    1-1-2013

    Document Type

    Article

    Language

    English

    First Page

    140

    Last Page

    150

    WOS Identifier

    WOS:000322207600018

    ISSN

    0277-5387

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