One dimensional coordination polymers: Synthesis, crystal structures and spectroscopic properties

Karaagac D., KÜRKÇÜOĞLU G. S., ŞENYEL M., ŞAHİN O.

JOURNAL OF MOLECULAR STRUCTURE, cilt.1123, ss.327-334, 2016 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1123
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1016/j.molstruc.2016.06.036
  • Dergi Adı: JOURNAL OF MOLECULAR STRUCTURE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.327-334
  • Anahtar Kelimeler: Tetracyanoplatinate(II) complex, Copper(II) complex, Zinc(II) complex, 4-(2-Aminoethyl)pyridine complex, Vibrational spectra, Crystal structure, TETRACYANONICKELATE COMPLEXES, FT-IR, MAGNETIC-PROPERTIES, THERMAL-PROPERTIES, HYDROGEN-BONDS, CYANO GROUPS, SPECTRA, TETRACYANOPLATINATE(II), LIGANDS, ETHYLENEDIAMINE
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

Two new one dimensional (1D) cyanide complexes, namely [M(4-aepy)(2)(H2O)(2)][Pt(CN)(4)], (4-aepy = 4-(2-aminoethyl)pyridine M = Cu(II) (1) or Zn(II) (2)), have been synthesized and characterized by vibrational (FT-IR and Raman) spectroscopy, single crystal X-ray diffraction, thermal and elemental analyses techniques. The crystallographic analyses reveal that 1 and 2 are isomorphous and isostructural, and crystallize in the monoclinic system and C2 space group. The Pt(II) ions are coordinated by four cyanide-carbon atoms in the square-planar geometry and the [Pt(CN)4]2 ions act as a counter ion. The M(II) ions display an N4O2 coordination sphere with a distorted octahedral geometry, the nitrogen donors belonging to four molecules of the organic 4-aepy that act as unidentate ligands and two oxygen atoms from aqua ligands. The crystal structures of 1 and 2 are similar each other and linked via intermolecular hydrogen bonding, Pt center dot center dot center dot pi interactions to form 3D supramolecular network. Vibration assignments of all the observed bands are given and the spectral features also supported to the crystal structures of the complexes. (C) 2016 Elsevier B.V. All rights reserved.