• Title/Summary/Keyword: Binuclear $Cu^I$ complex

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Epoxidation of Olefins by Iodosylbenzene Catalyzed by Non-Porphyrin Metal Complexes

  • Nam Wonwoo;Baek Seung Joong;Kazuko I. Liao;Joan Selverstone Valentine
    • Bulletin of the Korean Chemical Society
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    • v.15 no.12
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    • pp.1112-1118
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    • 1994
  • Epoxidation of olefins has been studied using iodosylbenzene (PhIO) as the terminal oxidant and binuclear and mononuclear complexes of $Mn^{2+}$, $Co^{2+}$, and $Cu^{2+}$ as catalysts. Epoxides were the predominant products with trace amounts of allylic oxidation products, and the metal complexes were found to be effective catalysts in the epoxidation reactions. The reactivity of binuclear copper complexes was greater than that of the mononuclear copper complexes, whereas the binuclear and mononuclear complexes of $Mn^{2+}$ and $Co^{2+}$ showed similar reactivities. The nature of the ligands bound to copper did not influence the reactivity of the binuclear copper complexes so long as copper ions were held in close proximity. A metal-iodosylbenzene complex, such as suggested previously for Lewis acidic metal complex-catalyzed epoxidation by iodosylbenzene, is proposed as the active epoxidizing species. Some mechanistic aspects are discussed as well.

Electrochemical Properties of Binuclear Tetradentate Schiff Base Cobalt(II), Nickel(II) and Copper(II) Complexes in Nonaqueous Solvents. (V) (비수용매에서 이핵성 네자리 Schiff Base Cobalt(II), Nickel(II) 및 Copper(II) 착물들의 전기화학적 성질 (제 5 보))

  • Chjo Ki-Hyung;Choi Yong-Kook;Lee Song-Ju;Kim Chan-Young;Rim Chae-Pyeong
    • Journal of the Korean Chemical Society
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    • v.36 no.5
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    • pp.709-719
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    • 1992
  • We synthesized the binuclear tetradentate Schiff base cobalt(II), nickel(II) and copper(II) complexes such as [Co(II)_2(TSBP)(L)_4], [Ni(II)_2(TSBP)(II)_4] and [Cu(II)_2(TSBP)] (TSBP: 3,3',4,4'-tetra(salicylideneimino)-1,1'-biphenyl, L: Py, DMSO and DMF). We identified the binucleated structure of these complexes by elemental analysis, IR-spectrum, UV-visible spectrum, T.G.A. and D.S.C. According to the results for cyclic voltammogram and differential pulse polarogram of 1 mM complexes in nonaqueous solvents included 0.1M TEAP-L (L; Py, DMSO and DMF) as supporting electrolyte, it was found that diffusionally controlled redox processes of four steps through with one electron for binucleated Schiff base Cobalt(II) complex was Co(III)_2 {^\longrightarrow \\_\longleftarrow^e^-}Co(III)Co(II)_2{^\longrightarrow \\_\longleftarrow^e^-}Co(II){^\longrightarrow \\_\longleftarrow^e^-}Co(I){^\longrightarrow \\_\longleftarrow^e^-}Co(I)_2 and two steps with one electron for Nickel(II) and Copper(II) complexes were M(II)_2 {^\longrightarrow \\_\longleftarrow^e^-}M(I)M(I){^\longrightarrow \\_\longleftarrow^e^-}M(I)_2 (M; Ni and Cu) in nonaqueous solvents.

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