Syntheses and structural studies on some new dithiophosphinato complexes of nickel(II), cobalt(II) and mixed pyridino complexes thereof

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Saglam E. G.

INORGANICA CHIMICA ACTA, cilt.434, ss.188-197, 2015 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 434
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1016/j.ica.2015.05.028
  • Dergi Adı: INORGANICA CHIMICA ACTA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.188-197
  • Marmara Üniversitesi Adresli: Hayır

Özet

Four different, alkyl(4-methoxyphenyl) dithiophosphinic acid metal complexes, namely, trans-bis[iso-propyl (4-methoxyphenyl) dithiophosphinato] nickel(II), 1; bis-{[iso-propyl (4-methoxyphenyl)dithiophosphinato]} cobalt(II), 2; bis-{[sec-butyl (4-methoxyphenyl)-dithiophosphinato]} cobalt(II), 3 and bis-{[iso-amyl (4-methoxyphenyl)-dithiophosphinato]} cobalt(II), 4 were prepared. As 1 and 2 were synthesized for the first time, their structures were also elucidated. Starting with these four-coordinated complexes, novel, mixed (pyridino) dithiophosphinic acid complexes of Ni(II) and Co(II) were also prepared. These complexes were characterized by elemental analysis and NMR (H-1-, C-13-, P-31-); MS; FTIR; and Raman spectroscopies. TGA and DTA data were also made use of to support the structures revealed by spectroscopy. The magnetic susceptibilities of the complexes were measured to confirm the hybridization patterns and the geometries. The crystal structures of the cobalt pyridino-DTPA complexes were analyzed. X-ray analyses show that the P-S bonds in the complexes are essentially of the same order; that is, electron delocalization prevails. (C) 2015 Elsevier B.V. All rights reserved.