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Synthesis and structural characterization of novel symmetric homodinuclear iridium acetylacetonate complexes

机译:新型对称同核乙酰丙酮铱铱配合物的合成与结构表征

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Two novel symmetric homodinuclear iridium acetylacetonate complexes were synthesized via the direct reaction of 2 equivalent [(acac-O,O)(2)(acac-C-3)Ir(III)(H2O)] with 1 equivalent of pyrazine or 4,4'-bipyridine. The structures were fully characterized by elemental analysis, H-1-NMR, and single-crystal X-ray diffraction. The structural data support that they have a highly symmetric dinuclear nature with two motifs containing iridium [(acac-O,O)(2)(acac-C-3) Ir(III)] bridged by two nitrogen atoms of pyrazine or 4,4'-bipyridine in a trans position. Absorption spectra of both compounds were measured and purple-shifted about 78.9 nm of the metal-to-ligand charge transfer transition was observed.
机译:通过2当量[(acac-O,O)(2)(acac-C-3)Ir(III)(H2O)]与1当量吡嗪或4的直接反应合成了两种新颖的对称同核乙酰丙酮铱铱配合物。 4'-联吡啶。通过元素分析,H-1-NMR和单晶X射线衍射对结构进行了充分表征。结构数据支持它们具有高度对称的双核性质,具有两个包含由吡嗪或2的氮原子桥接的铱[(acac-O,O)(2)(acac-C-3)Ir(III)]的基序。 4'-联吡啶处于反式位置。测量了两种化合物的吸收光谱,并且观察到金属-配体电荷转移跃迁的紫色位移为约78.9nm。

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