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Synthesis, electrochemistry and spectroscopic properties of ruthenium phthalocyanine and naphthalocyanine complexes with triphenylarsine ligands

机译:三苯基ar配体的钌酞菁和萘酞菁配合物的合成,电化学和光谱性质

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The synthesis, electrochemistry and spectroscopic properties of [PcRu(AsPh3)(2)] (1) and [{(tBu)(4)Nc}Ru(AsPh3)(2)] (2), where Pc = phthalocyanine and Nc = naphthalocyanine are reported. These complexes are the first examples of metal phthalocyanine and naphthalocyanine complexes with axially-coordinated arsine ligands. The AsPh3 ligands readily dissociate in non-coordinating solvents with 2 showing more rapid dissociation. In cyclic voltammetry experiments, 1 displayed three macrocycle-centred redox processes; one reduction and two oxidation processes. One reduction and three oxidation processes were observed for 2. The reduction and first oxidation are assigned to macrocycle-centred processes. The UV-Vis spectra of both complexes recorded over time showed macrocycle-centred oxidation. The oxidation was hindered by removing dioxygen from the solvent or adding excess AsPh3. (c) 2007 Elsevier B.V. All rights reserved.
机译:[PcRu(AsPh3)(2)](1)和[{(tBu)(4)Nc} Ru(AsPh3)(2)](2)的合成,电化学和光谱性质,其中Pc =酞菁,Nc =报道了萘酞菁。这些配合物是具有轴向配位的砷化氢配体的金属酞菁和萘酞菁配合物的第一个实例。 AsPh3配体容易在非配位溶剂中解离,其中2显示出更快的解离。在循环伏安法实验中,1显示了三个以大环为中心的氧化还原过程。一还原和二氧化过程。对于2观察到一个还原和三个氧化过程。还原和第一次氧化被分配给以大环为中心的过程。随时间记录的两种配合物的UV-Vis光谱均显示以大环为中心的氧化。通过从溶剂中除去双氧或添加过量的AsPh3可以阻止氧化。 (c)2007 Elsevier B.V.保留所有权利。

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