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Synthesis of Rigid pi-Conjugated Mono-, Bis-, Tris-, and Tetrakis(terpyridine)s: Influence of the Degree and Pattern of Substitution on the Photophysical Properties

机译:刚性π-共轭单,双,三和四吡啶(叔吡啶)的合成:取代的程度和模式对光物理性质的影响

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摘要

A series of rigid pi-conjugated mono-, bis-, tris-, and tetrakis(terpyridine)s 3-8 was synthesized in high yields by means of Horner-Wadsworth-Emmons (HWE) reactions between benzyl phosphonates 1 and an aldehyde-functionalized terpyridine derivative 2. The photophysical properties of the materials in solution and in the solid state depend strongly both on the numbers of terpyridine moieties attached to the central phenyl cores and on the geometries of the compounds. The photophysical behavior of the ortho-substituted compounds 5 and 8 indicated significant changes in the geometries, together with major extensions of the effective pi-conjugated systems upon excitation, Bright green emission with high quantum yields was observed for the tetrakis(terpyridine) derivative 8. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
机译:通过苄基膦酸酯1和醛-之间的霍纳-沃兹沃思-埃蒙斯(HWE)反应高收率合成了一系列刚性pi共轭单,双,三和四(吡啶)3-8功能化的吡啶吡啶衍生物2.溶液中和固态材料的光物理性质在很大程度上取决于与中央苯基核连接的叔吡啶部分的数量以及化合物的几何形状。邻位取代的化合物5和8的光物理行为表明,其几何形状发生了显着变化,并且有效的pi共轭体系在激发后发生了重大延伸,四(三吡啶)衍生物8的亮绿色发射具有高量子产率。 ((C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,德国,2009年)

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