4.1 Article

Synthesis, Characterization, and Luminescent Properties of a 3d Metal Coordination Polymer Based on Dicarboxylate Ligand and 1,10-Phenanthroline

Journal

RUSSIAN JOURNAL OF GENERAL CHEMISTRY
Volume 92, Issue 6, Pages 1115-1120

Publisher

MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S107036322206024X

Keywords

solvothermal synthesis; coordination polymer; dicarboxylate ligand; properties

Funding

  1. Scientific Research Fund Project of Liaoning Provincial Education Department [LJKZ0371]

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A novel manganese coordination polymer was synthesized through solvothermal reaction of MnSO4 with 2,2'-dithiodibenzoic acid and 1,10-phenanthroline in ethanol/DMF/H2O. The resulting compound consists of two chain structures linked by coordination water molecules and carboxylate groups, with L2- ligands bridging Mn ions to form a ladder-like structure. In the solid state, the compound exhibits luminescence at 598 nm and a redshift of 130 nm compared to the free H2L ligand, indicating charge transfer between ligands and metal ions. The compound also shows antiferromagnetic interactions between Mn ions.
Solvothermal reaction of MnSO4 with 2,2 '-dithiodibenzoic acid (H2L) and 1,10-phenanthroline (phen) in ethanol/DMF/H2O has resulted in a novel manganese coordination polymer [Mn(L)(phen)(H2O)(0.5)](n) (1). Compound 1 is built up of two chain structures derived from L2- ligands and Mn ions linked by coordination water molecules and the carboxylate groups of L2-. The L2- anions act as tridentate ligands bridging with Mn ions and generating a ladder-like structure comprised of left- and right-handed chains. In the solid state, compound 1 exhibits luminescence at 598 nm. In comparison with the free H2L ligand, compound 1 demonstrates 130 nm redshift, which can be attributed to charge transfer between ligands and metal ions. Compound 1 exhibits antiferromagnetic interactions between Mn ions.

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