Synthesis, crystal structure, and spectrothermal characterization of a novel dimeric cadmium(II) azobispyridine complex, [(mu-abpy){CdCl2(abpy)}(2)]center dot 0.86H(2)O

Arslan F., Ucar I., Bulut A., Olmez H., Odabasoglu M., Buyukgungur O.

ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, cilt.632, sa.8-9, ss.1606-1609, 2006 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 632 Sayı: 8-9
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1002/zaac.200600011
  • Dergi Adı: ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1606-1609
  • Anahtar Kelimeler: cadmium, azobispyridine, crystal structure, thermal analysis, ORGANOTIN(IV) DERIVATIVES, 2,2'-AZOPYRIDINE, SPECTROSCOPY, SPECTROELECTROCHEMISTRY, MOSSBAUER, ADDUCTS, LIGANDS, NETWORK, TIN(IV), EPR
  • Ondokuz Mayıs Üniversitesi Adresli: Hayır

Özet

The novel complex mu-2,2'-azobispyridine-bis[2,2'azobispyridinedichlorocadmium(II)].0.86 hydrate (1) was synthesized and characterized by elemental analysis, IR and UV-Vis spectroscopy, thermal analysis and X-ray diffraction techniques. The crystal structure analysis indicates that the Cd2+ ions have a distorted octahedral coordination with Cd-II-Cd-II distance of 5.929(7) angstrom. One of the azobispyridine (abpy) ligands acts as a 's-frame' bridging ligand which adopts an s-cis/E/s-cis conformation, while the others adopt an s-cis/E/s-trans conformation, coordinated to Cd2+ ions in a trans position. pi-pi and pi-ring interactions are responsible for crystal packing. The decomposition reaction takes place in the temperature range of 20-1000 degrees C in the static air atmosphere. Thermal decomposition of the title complex proceeds in five stages.