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Development of tris-cyclometalated iridium complexes for cellular imaging through structural modification

机译:通过结构改性,开发Tris-Cyclosalated铱络合物的细胞成像

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Herein we report the synthesis and investigation of two novel Iris-cyclometalated iridium complexes derived from [Ir(ppy)(3)] and bearing an aminoalkyl substituent on one of the 2-phenylpyridine ligands. These complexes differ in the number of the alkyl substituents of the aminoalkyl group. Specifically, the complexes reported herein contain one (1) and two (2) 2-hydroxy ethyl groups on the nitrogen atom. Both complexes retain the good photophysical properties reported for earlier versions of this group of Iris-cyclometalated iridium complexes. However, the differences in the substitution result in changes in the responsive photoluminescence behavior in aqueous solutions. Live cell microscopy experiments revealed that the complexes can localize in NIH-3T3 cells. Finally, it has been observed that the complex containing two 2-hydroxy ethyl groups is less cytotoxic than the its mono-substituted counterpart.
机译:在此,我们报告了来自[IR(PPY)(3)]的两种新型虹膜环状铱络合物的合成和研究,并携带氨基烷基取代基在2-苯基吡啶配体之一上。 这些复合物在氨基烷基的烷基取代基的数量中不同。 具体地,本文报道的复合物在氮原子上含有一种(1)和两(2)个羟基乙基。 两种复合物保留了本组IRIS-环状铱配合物的早期版本的良好的光学性质。 然而,取代的差异导致水溶液中响应式光致发光行为的变化。 活细胞显微镜实验表明,复合物可以在NIH-3T3细胞中定位。 最后,已经观察到含有两个2-羟基乙基的络合物比其单取代的对应物更少细胞毒性。

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