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Öğe The orthopalladation dinuclear [Pd(L1)(?-OAc)]2, [Pd(L2)(?-OAc)]2 and mononuclear [Pd(L3)2] complexes with [N, C, O] or [N, O] containing ligands: Synthesis, spectral characterization, electrochemistry and catalytic properties(Elsevier Science Sa, 2010) Kilic, Ahmet; Kilinc, Dilek; Tas, Esref; Yilmaz, Ismail; Durgun, Mustafa; Ozdemir, Ismail; Yasar, SedatTreatment of the salicylaldimine ligands (L1H, L2H, L3H, L4H and L5H) with palladium(II) acetate in absolute ethanol gave the orthopalladation dinuclear [Pd(L-1)(mu-OAc)](2), [Pd(L-2)(mu-OAc)](2) and mononuclear [Pd(L-3)(2)] with the tetradentate ligands [N, C, O] or [N, O] moiety. The ligands L1H and L2H are coordinated through the imine nitrogen and aromatic ortho carbon atoms, whereas the ligand L3H coordinated through the imine nitrogen and phenolic oxygens atoms. The Pd(II) complexes have a square-planar structure and were found to be effective catalysts for the hydrogenation of both nitrobenzene and cyclohexene. These metal complexes were also tested as catalysts in Suzuki-Miyaura coupling of aryl bromide in the presence of K2CO3. The catalytic studies showed that the introduction of different groups on the salicyl ring of the molecules effected the catalytic activity towards hydrogenation of nitrobenzene and cyclohexene in DMF at 25 and 45 degrees C. The Pd(II) complexes easily prepared from cheap materials could be used as versatile and efficient catalysts for different C-C coupling reactions (Suzuki-Miyaura reactions). The structure of ligands and their complexes was characterized by UV-Vis, FT-IR, H-1 and C-13 NMR, elemental analysis, molar conductivity, as well as by electrochemical techniques. (C) 2009 Elsevier B.V. All rights reserved.Öğe Synthesis, characterization, electrochemical behaviors and applications in the Suzuki-Miyaura cross-coupling reactions of N2S2O2 thio Schiff base ligand and its Cu(II), Co(III), Ni(II), Pd(II) complexes and their usage in the fabrication of organic-inorganic hybrid devices(Elsevier Science Sa, 2012) Temel, Hamdi; Pasa, Salih; Ocak, Yusuf Selim; Yilmaz, Ismail; Demir, Serpil; Ozdemir, IsmailThe thio Schiff base ligand N,N'-bis(o-hydroxy-1-naphtaldehydene)-1,2-bis(o-amino phenilthio)ethane (L) was synthesized by the condensation of o-hydroxy-1-naphthaldehyde and 1,2-bis(2-amino thiophenol)ethane. The reactions of the ligand with different transition metal(II) salts under reflux system condition afforded a series of metal complexes such as Cu(II), Co(III), Ni(II) and Pd(II). Ligand and its complexes were characterized by a combination of elemental analysis, UV-vis spectroscopy, FT-IR, H-1 NMR, MS and TGA/DTA. The electrochemical properties of L and [Cu(L)] were investigated using cyclic voltammetry (CV) in the solutions of dimethyl sulfoxide (DMSO). The catalytic property of thio Schiff base ligand with Suzuki cross-coupling reactions were also determined with different substituted aryl halides in the presence of aryl boronic acid and Pd(AcO)(2) as catalyst. In addition, the fabrication of organic-inorganic hybrid devices using L and its Co(III), Ni(II) and Pd(II) complexes and their electrical properties have been reported. (C) 2011 Elsevier B.V. All rights reserved.