Yazar "Buyukgungor, Orhan" seçeneğine göre listele

Listeleniyor 1 - 3 / 3
  • [ X ]
    Öğe
    Preparation and crystal structure of binuclear chloro{6-[[chloro(triphenylphosphine)platinum](mesitylimino)methyl]pyridin-2-yl}bis(triphenylphosphine)platinum(II)
    (Pergamon-Elsevier Science Ltd, 2008) Gunay, M. Emin; Dayan, Osman; Gokce, Aytac Gurhan; Aygun, Muhittin; Cetinkaya, Bekir; Buyukgungor, Orhan
    Treatment of N,N'-bis(mesityl)pyridine-2,6-carboxyimidoyldichloride, 1, in toluene solution with [Pt(PPh3)(4)] at 100 degrees C afforded a novel platinacyclic compound, 3, in 63% yield, instead of the expected compound 2. The molecular and crystal structures of the title compound, 3, have been determined by the single crystal X-ray diffraction technique. The coordination geometries around the Pt atoms are distorted square-planar. In the crystal structure, the molecules are linked by a pair of C-H center dot center dot center dot N hydrogen bonds into a centrosymmetric dinner with an R-2(2) (16) ring, centred at (1/2,1/2,1/2). (C) 2008 Elsevier Ltd. All rights reserved.
  • [ X ]
    Öğe
    Synthesis and catalytic activity of ruthenium(II) complexes containing pyridine-based tridentate triamines ('NNN') and pyridine carboxylate ligands (NO)
    (Elsevier Science Sa, 2012) Dayan, Osman; Ozdemir, Namik; Serbetci, Zafer; Dincer, Muharrem; Cetinkaya, Bekir; Buyukgungor, Orhan
    The reaction of [(p-cymene)RuCl2](2) with K[NOa-b] (NO- = 2-picolinate, a or 2-quinaldinate, b) gave neutral [(p-cymene)RuCl(NOa-b)] (1a-b), complexes which were treated with pyridine-based meridional triamine ligands ('NNN') to create complexes of the type [RuCl(NOa-b)('NNN')] (2a: 'N = N-d, NOa(-) = 2-picolinato; 2b: 'N = N-d, NOb- = 2-quinaldinato; 3a: 'N = N-b, NOa- = 2-picolinato; 3b: 'N = N-b, NOb- = 2-quinaldinato; 4a: 'N = N-p, NOa- = 2-picolinato; 4b: 'N = N-p, NOb- = 2-quinaldinato). The new compounds were characterized by elemental analysis, IR and NMR spectroscopy and, 1b was studied by single crystal X-ray diffraction. The complexes 1-4 have been employed as catalysts for the transfer hydrogenation (TH) of acetophenone derivatives to secondary alcohols in the presence of KOH using 2-propanol as a hydrogen source at 82 degrees C. The highest catalytic activity was obtained with 3a. (C) 2012 Elsevier B. V. All rights reserved.
  • [ X ]
    Öğe
    Synthesis and characterization of SiO2-supported ruthenium complexes containing aromatic sulfonamides: as catalysts for transfer hydrogenation of acetophenone
    (Royal Soc Chemistry, 2013) Dayan, Serkan; Kalaycioglu, Nilgun Ozpozan; Dayan, Osman; Ozdemir, Namik; Dincer, Muharrem; Buyukgungor, Orhan
    3-Amino-N-aryl-benzenesulfonamides (1-3) were successfully synthesized by the reaction of m-phenylenediamine and various benzenesulfonyl chlorides. Then, a series of ruthenium complexes (4-6) were prepared from the reaction of [RuCl2(p-cymene)](2) and 1-3. Finally, SiO2-supported Ru(II) complexes (7-9) were prepared by an impregnation method. The synthesized compounds and materials were characterized by different methods such as NMR, FT-IR, TG/DTA, nitrogen adsorption-desorption (BET), SEM and EDX. Also, the solid state structures of 4-6 were determined by single-crystal X-ray diffraction. 4-9 were used as catalysts for the transfer hydrogenation of acetophenone. 4-9 showed good catalytic activity and so the effects of the different groups were also examined. For the transfer hydrogenation of acetophenone, 7-9 had similar activity to 4-6. However, the longer lifetime of 7-9 makes them more advantageous than the non-supported catalysts (4-6) in terms of catalytic cycle. Therefore, the effect of SiO2 was investigated as a catalyst and the results show that excess silicon(IV) oxide was a surprisingly active catalyst for the hydrogenation of acetophenone under these conditions.