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Güveli Şükriye Özdemir Namık Bal-Demirci Tülay Soylu Mustafa Serkan Ülküseven Bahri 《Transition Metal Chemistry》2019,44(2):115-123
Transition Metal Chemistry - Mixed ligand Ni(II) complexes were synthesized from triphenylphosphine and S-methyl- or S-ethyl-isothiosemicarbazone ligands derived from... 相似文献
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Bahri Ülküseven Tülay Bal-Demirci Mehmet Akkurt erife Pnar Yaln Orhan Büyükgüngr 《Polyhedron》2008,27(18):3646-3652
The reactions of 5-R-2-hydroxybenzaldehyde-4-allyl-thiosemicarbazone {R: H (L1); Br (L2)} with [MII(PPh3)nCl2] (M = Ni, n = 2 and M = Ru, n = 3) in a 1:1 molar ratio have given stable solid complexes corresponding to the general formula [Ni(L)(PPh3)] and [Ru(HL)2(PPh3)2]. While the 1:1 nickel complexes are formed from an ONS donor set of the thiosemicarbazone and the P atom of triphenylphosphine in a square planar structure, the 1:2 ruthenium complexes consist of a couple from each of N, S and P donor atoms in a distorted octahedral geometry. These mixed-ligand complexes have been characterized by elemental analysis, IR, UV–Vis, APCI-MS, 1H and 31P NMR spectroscopies. The structures of [Ni(L2)(PPh3)] (II) and [Ru(L1H)2(PPh3)2] (III) were determined by single crystal X-ray diffraction. 相似文献
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Mixed-ligand zinc complexes with N,N,N′,N′-tetramethylethylenediamine (tmen) and R-salicylaldehyde N(4)-allyl thiosemicarbazones (R: 3-OCH3 (L1), 5-Br(L2)), [ZnL1,2(tmen)], were synthesized and the complexes were characterized by elemental analysis, atomic absorption spectrometer, magnetic susceptibility, molar conductivity, electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) mass spectra and IR, UV–Vis, 1H NMR and 15N spectroscopies. Crystal of [ZnL2(tmen)] have a slightly distorted square pyramid involving O, N, S atoms of thiosemicarbazone and one N atom of tmen in basal plane and the other N atom of tmen in apex of the pyramid. The non-coordinated allyl group is disordered. 相似文献
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Two uranyl complexes having the composition [UO2(L)DMSO] were synthesized using salicyl- and 3,5-dichlorosalicylaldehyde-S-propyl-thiosemicarbazones as starting materials. The S-propyl-thiosemicarbazidato structures in the complexes are N1-3,5-dichlorosalicylidene-N4-salicylidene and N1-salicylidene-N4-3,5-dichlorosalicylidene. The stable solid complexes were characterized by means of elemental analysis, IR and 1H NMR spectroscopies, and the single crystal X-ray diffraction technique. The two complexes, with the same formula, crystallize in different space groups. In the title complexes, the uranium atom is seven-coordinated in a distorted pentagonal-bipyramidal geometry involving an ONNO donor set of the thiosemicarbazidato ligand and an oxygen atom of a DMSO molecule. The two apical positions of the pentagonal bipyramid are occupied by the two oxygen atoms of the trans-dioxouranium group. The relative orientations of the DMSO and S-propyl groups in both complexes are somewhat different due to different crystal packing. 相似文献
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Tülay Bal-Demirci Mehmet Akkurt Şerife Pınar Yalçın Orhan Büyükgüngör 《Transition Metal Chemistry》2010,35(1):95-102
Mixed-ligand ternary cobalt(III) complexes consisting of N,N,N′,N′-tetramethylethylenediamine (tmen), R-salicylaldehyde-N(4)-allyl/methyl
thiosemicarbazones (R=3-OMe (LI/LII) or H (LIII/LIV) and azide, of general formula [CoL(tmen)(N3)], were synthesized and characterized by physico-chemical and spectroscopic methods. The crystal structure of [CoLI(tmen)(N3)] has a slightly distorted octahedral coordination geometry involving the O, N and S atoms of thiosemicarbazone. 相似文献
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Şükriye Güveli Tülay Bal-Demirci Namık Özdemir Bahri Ülküseven 《Transition Metal Chemistry》2009,34(4):383-388
Reactions of 5-bromo-2-hydroxy-benzaldehyde-S-R-4-R1-thiosemicarbazones, [R, R1 = H,H (L1); CH3, H (L2); H, C6H5 (L3); CH3, C6H5 (L4)] with [Ni(PPh3)2Cl2] in 1:1 molar ratio yielded complexes of general formula [Ni(L)(PPh3)]. While the complexes of L1 and L3 involve the ONS donor set of the thiosemicarbazone, the L2 complexes utilize the ONN set. The reaction of L4 and the nickel salt gave the L3 complex by loss of the CH3 group from the sulphur. The complexes were characterized by physico-chemical and spectroscopic methods. The structures of
the L1 and L2 complexes have been determined by single crystal X-ray diffraction and a new coordination mode (ONN) of salicylaldehyde thiosemicarbazones
has been identified.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
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Sahin M Koca A Ozdemir N Dinçer M Büyükgüngör O Bal-Demirci T Ulküseven B 《Dalton transactions (Cambridge, England : 2003)》2010,39(42):10228-10237
The stable uranyl complexes, [UO(2)(L)C(9)H(19)OH], were obtained from 3,5-dichlorosalicyl-(L(I)) and salicyl-aldehyde-S-propyl-thiosemicarbazones (L(II)) with substituted-salicylaldehyde in nonyl alcohol. The structures of the complexes have been characterized by elemental analysis, IR, (1)H NMR, conductivity, magnetic moment measurements, cyclic voltammetry, thermal gravimetric analysis and single crystal X-ray diffraction technique. The U(VI) centre is seven-coordinated in a distorted pentagonal bipyramidal geometry. The relative orientations of the nonyl alcohol and S-propyl group in the title complexes are completely different due to different crystal packing. Electrochemical behaviors of the thiosemicarbazone ligands and the uranyl complexes were studied using cyclic voltammetry and square wave voltammetry. Redox processes of the compounds are significantly influenced by the central metal ions and the nature of substituents on the thiosemicarbazones, which are important factors in controlling the redox properties. In situ spectroelectrochemical studies were employed to determine the colors and spectra of electro-generated species of the complexes. 相似文献
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Şükriye Güveli Namık Özdemir Tülay Bal-Demirci Bahri Ülküseven Muharrem Dinçer Ömer Andaç 《Polyhedron》2010
Reaction of 2-hydroxyacetophenone thiosemicarbazone with [Ni(PPh3)2Cl2] in optimized conditions afforded a mixed ligand complex with an isolated triphenylphosphine molecule. The structure was characterized by elemental analysis, IR, NMR and UV–Vis. spectroscopies and single crystal X-ray diffraction technique. In addition, the molecular geometry, vibrational frequencies and gauge including atomic orbital (GIAO) 1H and 13C NMR chemical shift values of the title compound in the ground state have been calculated using the density functional theory (DFT/B3LYP) method with the 6-31G(d,p) basis set for the C, N, O, S, P, H atoms and LANL2DZ pseudo-potential for the Ni atom, and compared with the experimental data. Besides, atomic charge distributions, molecular electrostatic potential and frontier molecular orbitals (FMO) analysis of the title compound were investigated by theoretical calculations. The thermodynamic properties of the compound at different temperatures have been calculated and corresponding relations between the properties and temperature have also been obtained. Atomic charge distributions indicate that during forming the title compound, the free ligand of thiosemicarbazone ion transfers their negative charges to central Ni(II) ion. The effect of different solvents (chloroform, methanol and water) on the geometry, vibrational frequencies, total energies and dipole moments was studied using the density functional theory (DFT/B3LYP) method by applying the Onsager and the Polarizable Continuum Model (PCM). 相似文献
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