Karmis Rebecca E, Carrara Serena, Baxter Amy A, Hogan Conor F, Hulett Mark D, Barnard Peter J
Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Victoria, 3086, Australia.
Dalton Trans. 2019 Jul 9;48(27):9998-10010. doi: 10.1039/c9dt01362h.
A series of imidazolium salt, N-heterocyclic carbene (NHC) ligand precursors, combined with 1,2,3-triazoles were synthesized using the Cu(i) catalyzed azide-alkyne cycloaddition 'click reaction'. These pro-ligands were prepared from imidazolium molecules that were functionalized with either a terminal alkyne or azide group. Methylation of the triazole unit with methyl iodide produced a series of imidazolium/triazolium NHC pro-ligands. From these pro-ligands a family of luminescent Ir(iii) complexes of the general form [Ir(ppy)2(C^N)]+ or [Ir(ppy)2(C^C)]+ (where ppy is 2-phenylpyridine and C^N represents a bidentate imidazolylidene/triazole ligand and C^C represents a bidentate imidazolylidene/triazolylidene ligand) were prepared. The electrochemical, photophysical and electrochemiluminescence properties of the complexes have been evaluated and a preliminary study of two of these compounds as luminescent probes for cell imaging studies was conducted in A549 human lung adenocarcinoma basal epithelial cells. Co-localisation studies with the commercial dye MitoTracker CMXRos were consistent with mitochondrial uptake for these compounds.
利用铜(I)催化的叠氮化物-炔烃环加成“点击反应”合成了一系列咪唑盐、N-杂环卡宾(NHC)配体前体,并与1,2,3-三唑结合。这些前体配体由用末端炔基或叠氮基官能化的咪唑分子制备。用甲基碘对三唑单元进行甲基化反应生成了一系列咪唑鎓/三唑鎓NHC前体配体。由这些前体配体制备了通式为[Ir(ppy)2(C^N)]+或[Ir(ppy)2(C^C)]+的发光Ir(III)配合物家族(其中ppy为2-苯基吡啶,C^N代表双齿咪唑亚基/三唑配体,C^C代表双齿咪唑亚基/三唑亚基配体)。对这些配合物的电化学、光物理和电化学发光性质进行了评估,并在A549人肺腺癌基底上皮细胞中对其中两种化合物作为细胞成像研究的发光探针进行了初步研究。与商业染料MitoTracker CMXRos的共定位研究表明这些化合物定位于线粒体。