Synthesis, crystal structures, magnetic properties and Suzuki and Heck coupling catalytic activities of new coordination polymers containing tetracyanopalladate(II) anions

ŞENOCAK A., KARADAĞ A., Yerli Y., GÜRBÜZ N., ÖZDEMİR İ., ŞAHİN E.

POLYHEDRON, cilt.49, sa.1, ss.50-60, 2013 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 49 Sayı: 1
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1016/j.poly.2012.09.030
  • Dergi Adı: POLYHEDRON
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.50-60
  • Anahtar Kelimeler: Coordination polymers, Palladium complexes, Crystal structures, Thermal analysis, Magnetic susceptibility, Catalyst, BRIDGED BIMETALLIC COMPLEXES, HOST-GUEST CHEMISTRY, THERMAL-PROPERTIES, MOLECULAR SQUARE, ELECTRONIC-PROPERTIES, PALLADIUM CATALYSTS, ARYL BROMIDES, IR-SPECTRA, PT-PT, STEREOCHEMISTRY
  • Atatürk Üniversitesi Adresli: Evet

Özet

Four novel coordination polymers, [Ni(bishydeten)Pd(CN)(4)] (1), [Cu(bishydeten)Pd(CN)(4)] (2), [Zn(bishydeten)Pd(CN)(4)] (3) and [Cd(bishydeten)Pd(CN)(4)] (4) (bishydeten = N,N'-bis(2-hydroxyethyl)ethylenediamine], have been synthesized and characterized by various techniques (elemental analysis, IR, EPR, X-ray and thermal analysis). In compound 4, all of the cyano groups use -N edges to form coordination bonds to Cd(II) in addition to -C atoms, resulting in the formation of a tridimensional network. The same situation is observed for compound 3 for one of the tetracyanopalladate(II) groups, while two cyano groups remain in the monodentate form coordinated to Pd(II) in the other tetracyanopalladate(II) group. While an EPR signal was not observed for 1, the g parameters obtained from the EPR spectrum of 2 indicated that the Cu(II) ions are located in tetragonal distorted octahedral sites (D-4h) and that the ground state of the paramagnetic electron is d(x2-y2). Variable temperature magnetic susceptibility measurements recorded in the range 15-300 K showed the presence of a very small antiferromagnetic interaction below 20 K for complexes 1 and 2.2 was proven to be less effective as a catalyst than 1 under the Heck reaction conditions. Moreover, 1 was determined to be a more effective catalyst and more efficient for iodoarenes than bromoarenes under Suzuki coupling conditions. (c) 2012 Elsevier Ltd. All rights reserved.