Hydrothermal synthesis, structure, heterogeneous catalytic activity and photoluminescent properties of a novel homoleptic Sm(III)-organic framework

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AY B., YILDIZ E., Felts A. C., Abboud K. A.

JOURNAL OF SOLID STATE CHEMISTRY, cilt.244, ss.61-68, 2016 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 244
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1016/j.jssc.2016.09.018
  • Dergi Adı: JOURNAL OF SOLID STATE CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.61-68
  • Anahtar Kelimeler: Hydrothermal Synthesis, Luminescence, 2,6-pyridinedicarboxylic acid, Sm(III) Coordination Polymer, Heterogeneous Catalysis, Thymoquinone, LANTHANIDE COORDINATION POLYMERS, METAL-ORGANIC FRAMEWORKS, CRYSTAL-STRUCTURE, LUMINESCENT PROPERTIES, SOFT ACIDS, PIPERAZINE, LIGANDS, MONOTERPENES, OXIDATION, PYRIDINE
  • Çukurova Üniversitesi Adresli: Evet

Özet

A novel metal-organic framework, (H(2)pip)(n)[Sm-2(pydc)(4)(H2O)(2)](n) (1) (H(2)pydc=2,6-pyridinedicarboxylic acid, H(2)pip=piperazine) has been synthesized under hydrothermal conditions and characterized by the elemental analysis, inductively coupled plasma (ICP) spectrometer, fourier transform infrared (FT-IR) spectra, thermogravimetric analysis (TGA), single crystal X-ray diffraction analysis and powder X-ray diffraction (PXRD). The structure of 1 was determined to be three-dimensional, linked along Sm-O-Sm chains. The asymmetric unit consisted of one singly anionic fragment consisting of Sm(III) coordinated to two H(2)pydc ligands and one water, and one half of a protonated H(2)pip, which sits on an inversion center. 1 exhibited luminescence emission bands at 534 nm at room temperature when excited at 440 nm. Its thermal behavior and catalytic performance were investigated and the selectivity was measured as 100% for the oxidation of thymol to thymoquinone. (C) 2016 Elsevier Inc. All rights reserved.