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多吡啶修饰的 Fe(II) 和 Ru(II) 配合物的 Pd(0)催化交叉偶联反应:金属超分子组装的新构筑块。

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

机构信息

State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.

出版信息

Dalton Trans. 2013 Nov 28;42(44):15625-36. doi: 10.1039/c3dt52331d.

Abstract

Eight metal complexes of the type M(tpy)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 core essentially unaffected. The binding of metal ions by the free pyridines is also demonstrated as means of assembling larger ordered non-covalent structures.

摘要

报道了 8 种M(tpy)2(tpy = 2,2':6',2''-三联吡啶)类型的金属配合物,它们具有四个悬垂吡啶环,通过 NMR、MS、吸收光谱和电化学方法进行了表征。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)配合物上均以较高产率进行。悬垂吡啶单元的易 N-烷基化对配合物的吸收和电化学还原有显著影响,这些过程定位于外围,而 Ru(tpy)2核心基本不受影响。游离吡啶与金属离子的结合也被证明是组装更大有序非共价结构的一种手段。

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