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Multi-pyridine decorated Fe(ii) and Ru(ii) complexes by Pd(0)-catalysed cross couplings: new building blocks for metallosupramolecular assemblies

机译:Pd(0)催化交叉偶联的多吡啶修饰的Fe(ii)和Ru(ii)配合物:金属超分子组装的新构件

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摘要

Eight metal complexes of the type [M(tpy)2]2+ (tpy = 2,2′:6′,2′′-terpyridine) featuring four pendant pyridine rings are reported and characterised by NMR, MS, absorption spectroscopy and electrochemical methods. Palladium-mediated Suzuki and Sonogashira cross-coupling reactions were performed on both free 4′-(3,5- dibromophenyl)-tpy and its Ru(ii) complex in good yields. The ready N-alkylation of the pendant pyridyl units has significant influence on the absorption and electrochemical reduction of the complexes, processes which are localised on the periphery and leaves the [Ru(tpy)2]2+ core essentially unaffected. The binding of metal ions by the free pyridines is also demonstrated as means of assembling larger ordered non-covalent structures. This journal is
机译:报道了具有四个侧吡啶环的八种[M(tpy)2] 2+(tpy = 2,2':6',2''-叔吡啶)类型的金属配合物,并通过NMR,MS,吸收光谱和电化学表征方法。钯介导的Suzuki和Sonogashira交叉偶联反应在游离​​4'-(3,5-二溴苯基)-tpy及其Ru(ii)络合物上均以良好的收率进行。吡啶基侧基单元的现成的N-烷基化对络合物的吸收和电化学还原具有显着影响,该过程位于外围并且使[Ru(tpy)2] 2+核基本不受影响。游离吡啶与金属离子的结合也被证明是组装更大的有序非共价结构的手段。这本日记是

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