Abstract <p>New complexes, (TBA)<sub>2</sub>[Mo<sub>6</sub>I<sub>8</sub>(OOC–C<sub>6</sub>H<sub>4</sub>–COOH)<sub>6</sub>] (<b>I</b>) and (TBA)<sub>2</sub>[Mo<sub>6</sub>I<sub>8</sub>(OOC–C<sub>5</sub>H<sub>4</sub>NO)<sub>6</sub>] (<b>II</b>), were synthesized by the reaction of (TBA)<sub>2</sub>[Mo<sub>6</sub>I<sub>8</sub>(OAc)<sub>6</sub>] with terephthalic acid and isonicotinic <i>N</i>-oxide acid, respectively. The optimized synthesis of complex <b>II</b> involves microwave activation of the reaction mixture at 130°C in a Teflon reactor using an ETHOS UP Milestone microwave system. According to X-ray structural analysis, the molybdenum atoms in the cluster cores of <b>I</b> and <b>II</b> are coordinated by carboxylate ligands in a monodentate fashion. The cluster anions [Mo<sub>6</sub>I<sub>8</sub>(OOC–C<sub>6</sub>H<sub>4</sub>–COOH)<sub>6</sub>]<sup>2–</sup> of complex <b>I</b> are arranged into a three-dimensional framework, and the crystal structure contains solvate molecules. Complexes <b>I</b> and <b>II</b> were characterized by elemental analysis for C, H, and N, IR spectroscopy, electrospray mass spectrometry, and proton nuclear magnetic resonance. The powder samples of <b>I</b> and <b>II</b> exhibit intense phosphorescence with emission maxima at ~680 nm, φ = 15%, τ = 125 µs (<b>I</b>) and φ = 12%, τ = 137&#xa0;µs (<b>II</b>) (under air at λ<sub>exc</sub> = 440 nm).</p>

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Terephthalate and Isonicotinate N-Oxide Complexes of the {Mo6I8}4+ Cluster

  • M. A. Mikhaylov,
  • T. S. Sukhikh,
  • D. G. Sheven’,
  • E. Kh. Sadykov,
  • M. N. Sokolov,
  • A. S. Berezin,
  • K. A. Tagil’tsev

摘要

Abstract

New complexes, (TBA)2[Mo6I8(OOC–C6H4–COOH)6] (I) and (TBA)2[Mo6I8(OOC–C5H4NO)6] (II), were synthesized by the reaction of (TBA)2[Mo6I8(OAc)6] with terephthalic acid and isonicotinic N-oxide acid, respectively. The optimized synthesis of complex II involves microwave activation of the reaction mixture at 130°C in a Teflon reactor using an ETHOS UP Milestone microwave system. According to X-ray structural analysis, the molybdenum atoms in the cluster cores of I and II are coordinated by carboxylate ligands in a monodentate fashion. The cluster anions [Mo6I8(OOC–C6H4–COOH)6]2– of complex I are arranged into a three-dimensional framework, and the crystal structure contains solvate molecules. Complexes I and II were characterized by elemental analysis for C, H, and N, IR spectroscopy, electrospray mass spectrometry, and proton nuclear magnetic resonance. The powder samples of I and II exhibit intense phosphorescence with emission maxima at ~680 nm, φ = 15%, τ = 125 µs (I) and φ = 12%, τ = 137 µs (II) (under air at λexc = 440 nm).