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首页> 外文期刊>Inorganica Chimica Acta >Cyclometalated ruthenium(II) carbonyl complexes containing 2-(biphenylazo)phenolate ligands: Synthesis, structure, DFT study and catalytic activity towards oxidation and transfer hydrogenation
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Cyclometalated ruthenium(II) carbonyl complexes containing 2-(biphenylazo)phenolate ligands: Synthesis, structure, DFT study and catalytic activity towards oxidation and transfer hydrogenation

机译:含有2-(Biphazo)酚酸盐配体的环状氧化钌(II)羰基配合物:用于氧化和转移氢化的合成,结构,DFT研究和催化活性

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2-(Biphenylazo)phenol ligands with various functional groups at the para-position of the phenol moiety (R = CH3, H2L1; R = OCH3, H2L2; R = (CH3)(3)C, H2L3; R = Cl, H2L4) readily undergo, upon reaction with [RuHCl (CO)(EPh3)(3)] (E = P, As) in toluene, cyclometalation via a C-H bond activation at the ortho-position to afford complexes of general formula [Ru(L)(CO)(EPh3)(2)] (E = P, L= L-1, 1; E= P, L= L-2, 2; E= P, L= L-3, 3; E = P, L = L-4 , 4; E = As, L = L-1, 5; E = As, L = L-2, 6; E = As, L = L-3, 7; E = As, L = L-4, 8). The molecular structure of five complexes has been determined by single-crystal X-ray structure analysis. In each complexes, the 2-(biphenylazo)phenol ligand is coordinated to the metal center as a di-anionic tridentate CNO-ligand with two triphenylphosphine/triphenylarsine in the axial positions along with one carbonyl group in the plane of the CNO- ligand. These new cyclometalated 2-(biphenylazo)phenolate complexes show intense absorption in the visible and ultraviolet regions and the nature of these transitions has been analyzed by TD-DFT calculations. The redox behavior of the complexes was also studied by cyclic voltammetry, revealing an irreversible reduction of the metallic center. The cyclometalated ruthenium(II) complexes were used as catalysts for oxidation and transfer hydrogenation reactions and they were found to be active catalysts. (C) 2018 Elsevier B.V. All rights reserved.
机译:2-(Biphylazo)苯酚配体,具有各种官能团的苯酚部分(R = CH3,H 2L1; R = OCH3,H 2L 2; R =(CH 3)(3)C,H 2L 3; R = CL,H2L4 )在与甲苯中的[RuHCl(CO)(Eph3)(3)(3)(3)(3))(E = P)](E = P)的反应中,通过在邻位的CH键活化的环荷常温,得到通式的复合物[Ru(l )(CO)(Eph3)(2)](E = P,L = L-1,1; E = P,L = L-2,2; E = P,L = L-3,3; E = p,l = l-4,4; e = aS,l = l-1,5; e = aS,l = l-2,6; e = aS,l = l-3,7; e = as, l = l-4,8)。通过单晶X射线结构分析确定了五种复合物的分子结构。在每种络合物中,2-(联苯氧氮杂)酚配体与金属中心配位,作为二阴离子三齿的CNO-配体,其在轴向位置中具有两个三苯基膦/三苯基甲串以及在CNO-配体的平面中的一个羰基。这些新的环荷芳化2-(Biphenylazo)酚盐配合物在可见和紫外线区域中显示出强烈的吸收,并通过TD-DFT计算分析了这些转变的性质。循环伏安法还研究了复合物的氧化还原行为,揭示了金属中心的不可逆减少。用氧化和转移氢化反应的催化剂用作催化剂的环荷芳化的钌(II)配合物,并发现它们是活性催化剂。 (c)2018年elestvier b.v.保留所有权利。

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