4.7 Article

Crystal Structure Diversities Based on 4,4′-(2,3,6,7-Tetramethoxyanthracene-9,10-diyl)dibenzoic Acid: From 2D Layer to 3D Net Framework

Journal

CRYSTAL GROWTH & DESIGN
Volume 12, Issue 12, Pages 6215-6222

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cg301403w

Keywords

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Funding

  1. NSFC (National Natural Science Foundation of China) [90922014]
  2. Shandong Natural Science Fund for Distinguished Young Scholars [JQ201003]
  3. Independent Innovation Foundation of Shandong University [2010JQ011]

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Five metal-organic coordination complexes with the formulas of {Mn(L)(H2O)(2)}(n) (1), {[Cd1.5L1.5(DEF)(2)]center dot 2DEF}(n) (2), [Co-1.5(L)(1.5)(H2O)](n) (3), {[Co(L)(H2O)(2)]center dot 4H(2)O}(n) (4), and {[Ni(L)(H2O)(2)]center dot 4H(2)O}(n) (5), (H2LOMe = 4,4'-(2,3,6,7-tetramethoxyanthracene-9,10-diyl)dibenzoic acid) based on a new rigid dicarboxylate ligand were synthesized and structurally characterized. Structural analysis reveals that H2LOMe acts as multibidentate bridging linker to connect metal ions and possesses similar coordination modes with terephthalic acid. Complex 1 is a (4(4))-sql layer incorporating bidentate-bridging H2LOMe and infinite Mn-(CO2)(2) SBUs. Complexes 2 and 3 have similar 2D (3(6))-hxl layer topology structure based on bidentate-chelating/bridging H2LOMe ligand and trinuclear hourglass SBUs. Complexes 4 and 5 are isostructural and possess 3D open frameworks based on infinite M-(mu(2)-H2O) chain. From the viewpoint of crystal structure diversity and comparison, our results further demonstrate that the coordination mode of metal ions and ligand are the vital elements in determining the final crystal structure. Moreover, thermal stabilities of 1-5 and temperature-dependent photoluminescence behaviors of 1 and 2 are discussed.

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