<p>Condensation of 8-hydroxy-2-quinolinecarbaldehyde and 3-bromoaniline, followed by reduction with NaBH<sub>4</sub>, afforded a new potential tridentate ligand of 2-(((3-bromophenyl)amino)methyl)quinolin-8-ol (<b>HL</b>), which was characterized by NMR spectroscopies and mass spectrometry. Treatment of <b>HL</b> with zinc acetate or cadmium acetate using solvothermal method gave a dinuclear complex [Zn<sub>2</sub>(κ<sup>2</sup>-<i>N</i>,<i>O</i>-<b>L</b>)<sub>2</sub>μ-(κ<sup>2</sup>-<i>N</i>,<i>O</i>-<b>L</b>)<sub>2</sub>]·2CH<sub>4</sub>O (<b>1</b>) and a tetranuclear complex [Cd<sub>4</sub>μ-(κ<sup>2</sup>-<i>N</i>,<i>O</i>-<b>L</b>)<sub>4</sub>μ-(κ<sup>3</sup>-<i>N,N</i>,<i>O</i>-<b>L</b>)<sub>2</sub>(κ<sup>2</sup>-O<sub>2</sub>CCH<sub>3</sub>)<sub>2</sub>] (<b>2</b>), respectively. The crystal structures of complexes <b>1</b> and <b>2</b> were determined with single-crystal X-ray diffractions and powder X-ray diffractions, showing the good ligating property and rich coordination modes of the ligand <b>L</b><sup>−</sup>. Moreover, the complexes <b>1</b>, <b>2</b> were characterized by infrared, NMR, UV–vis spectroscopies and mass spectrometry.</p>

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Synthesis, structures and properties of zinc and cadmium complexes with arylamine-modified 2-substituted 8‑hydroxyquinoline

  • Lan-Fang Geng,
  • Ai-Quan Jia

摘要

Condensation of 8-hydroxy-2-quinolinecarbaldehyde and 3-bromoaniline, followed by reduction with NaBH4, afforded a new potential tridentate ligand of 2-(((3-bromophenyl)amino)methyl)quinolin-8-ol (HL), which was characterized by NMR spectroscopies and mass spectrometry. Treatment of HL with zinc acetate or cadmium acetate using solvothermal method gave a dinuclear complex [Zn22-N,O-L)2μ-(κ2-N,O-L)2]·2CH4O (1) and a tetranuclear complex [Cd4μ-(κ2-N,O-L)4μ-(κ3-N,N,O-L)22-O2CCH3)2] (2), respectively. The crystal structures of complexes 1 and 2 were determined with single-crystal X-ray diffractions and powder X-ray diffractions, showing the good ligating property and rich coordination modes of the ligand L. Moreover, the complexes 1, 2 were characterized by infrared, NMR, UV–vis spectroscopies and mass spectrometry.