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首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis and Characterization of Phthalocyaninatometal (PcM, M=Fe2+, Co2+) Complexes with Monodentate Aromatic Isocyanide Ligands
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Synthesis and Characterization of Phthalocyaninatometal (PcM, M=Fe2+, Co2+) Complexes with Monodentate Aromatic Isocyanide Ligands

机译:单齿芳族异氰酸酯配体的酞菁金属(PcM,M = Fe2 +,Co2 +)配合物的合成与表征

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Metallophthalocyanines [PcM, Pc: phthalocyanine, M: Fe 2+ , Co 2+ ] were reacted with メ-isocyanonaphthalene( メ-in) and メ-isocyanoanthracene (メ-ia) to form monomeric complexes. The synthesis and coordination behaviour of the isocyanides as a ligand (L) are discussed. All the products were characterized by spectroscopic methods and instrumental analysis. The electrical conductivities of these complexes, which were not treated with dopant, were attributed to the metal-ligand electron delocalization in the PcML2 complexes. The complexes have an enlarged macrocycle where the ヰ-electron back donating ability of PcM is stronger than the ヲ-electron coordinating ability of the isonitrile ligands. Their electrical conductivities were measured as ヲRT = 2.1】10 -9 ~3】10 -10 S/cm. Also thermal stability was investigated in this study.
机译:使金属酞菁[PcM,Pc:酞菁,M:Fe 2+,Co 2+]与メ-异氰基萘(メ-in)和メ-异氰基蒽(メ-ia)反应形成单体配合物。讨论了异氰酸酯作为配体(L)的合成和配位行为。所有产品均通过光谱法和仪器分析表征。这些未经过掺杂剂处理的配合物的电导率归因于PcML2配合物中金属-配体电子的离域作用。配合物具有较大的大环,其中PcM的ヰ电子返电子能力强于异腈配体的ヲ电子配位能力。它们的电导率测量为asRT = 2.1】10 -9〜3】10 -10 S / cm。在这项研究中还研究了热稳定性。

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