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| 1 | Co-occurrence Network of Reuters News显示文摘 | oZGuR Arzucan Burak Cetin BINGOL Haluk | 2008 | Intemational Journal of Modem Physics C2008，19，5： | 1 |
| 2 | A Cultural Market Model显示文摘 | Amac Herdagdelen Haluk Bingol | 2008 | International Journal of Modern Physics2008，，2： | 1 |
| 3 | New Copper(Ⅱ) and Nickel(Ⅱ) Complexes of 4-Morpholinoacetophenone Thiosemicarbazone: Structural, Electrochemical and Antimicrobial Studies显示文摘 | BINGOL Haluk COSKUN Ahmet AKGEMCI Emine Guler KAYA Basturk ATALAY Tevfik | 2007 | Chinese Journal of Chemistry2007，25，3： | 1 |
| 4 | Investigation of the Lipophilicity of 2-Benzoylpyridine-Thiosemicarbazone Based on the Ion Transfer across the Liquid/Liquid Interface显示文摘The ion transfer reaction of 2-benzoylpyridine-thiosemicarbazone (HL), which has antimicrobial and antifungal properties and anticancer activity, has been studied to determine its lipophilicity by cyclic voltammetry at the water/1,2-dichloroethane (1,2-DCE) interface. The physicochemical parameters such as standard partition coefficient (lgPI)andthestandardGibbsenergyoftransfer('G0tr,,wI 'o)oftheprotonatedformoftheligandwere measured asa function of pH in aqueous phase. The protonated form of the ligand exhibited reversible or quasi-reversible voltammograms at the1,2-DCEintherangeofpH1-5.Theprotonationconstantsoftheligand,pKa1andpKa2,weredeterminedspectrophotometrically and were found to be 12.14 and 3.24, respectively. The standard Gibbs energy of transfer ('G0tr,,wN' o) and the partition coefficient of neutral species (lgPN) were also determined by the shake-flask method. The standard Gibbs energy of transfer of this compound across the water/1,2-DCE interface was evaluated as the quantitative measure of its lipophilicity. The difference between lgPI and lgPN was related to the degree of charge delocalization and was used to evaluate qualitatively the lipophilicity of the ligand. | AKGEMCI Emine G BINGOL Haluk OZCELIK Mehmet ERSOZ Mustafa | 2008 | 物理化学学报2008，24，4： | 1 |
| 5 | 噻二嗪衍生物的合成及Pb^(2+)在水/1,2-二氯乙烷界面转移的电化学性质(英文)显示文摘The transfer of Pb2+ facilitated by interfacial complexation with 5-(4-phenoxyphenyl)-6H-1,3,4-thiadiazin-2-amine(PPTA) at the polarized water/1,2-dicholoroethane(1,2-DCE) interface was investigated by cyclic voltammetry.We synthesized the thiadiazine derivative,PPTA,firstly.The transfer was performed at different metal concentrations and scan rates,and the obtained voltammetric transfer peaks toward Pb2+ ion over other divalent cations(Zn2+,Co2+,Ni2+,Cd2+,Hg2+,and Cu2+) were reversible.The dependence of the half-wave potentials of the Pb2+ ion on the concentration of PPTA in the organic phase indicates that the ion transfer is facilitated by the formation of 1:2(metal:ligand) complex in the organic phase with the association constant(lgβ2) of(17.1±0.2). | BASLAK Canan BINGOL Haluk COSKUN Ahmet ATALAY Tevfik | 2011 | 物理化学学报2011，27，8： | 0 |
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