Lo Kenneth Kam-Wing, Chung Chi-Keung, Zhu Nianyong
Department of Biology and Chemistry City University of Hong Kong Tat Chee Avenue, Kowloon, Hong Kong.
Chemistry. 2003 Jan 20;9(2):475-83. doi: 10.1002/chem.200390050.
We report the synthesis, characterization, photophysical, and electrochemical properties of a series of luminescent cyclometalated iridium(III) complexes containing two aldehyde functional groups Ir(pba)(2)(N-N) (Hpba=4-(2-pyridyl)benzaldehyde; N-N=2,2'-bipyridine, bpy (1), 1,10-phenanthroline, phen (2), 3,4,7,8-tetramethyl-1,10-phenanthroline, 3,4,7,8-Me(4)-phen (3), 4,7-diphenyl-1,10-phenanthroline, 4,7-Ph(2)-phen (4)). The X-ray crystal structure of complex 1 has been investigated. Upon photoexcitation, complexes 1-4 exhibit intense and long-lived emission in fluid solutions at 298 K and in low-temperature glass. The luminescence is assigned to a triplet intra-ligand ((3)IL) excited state associated with the pba(-) ligand, probably with mixing of some triplet metal-to-ligand charge-transfer ((3)MLCT) (dpi(Ir)-->pi*(pba(-))) character. Since each of these complexes possesses two aldehyde groups, which can react with the primary amine groups of biomolecules to form stable secondary amines after reductive amination, we have investigated the possibility of these complexes as novel luminescent cross-linkers for biological substrates. L-Alanine has been labeled with complexes 1-4 to give the luminescent bioconjugates 1-(Ala)(2)-4-(Ala)(2). These conjugates show strong photoluminescence with long emission lifetimes under ambient conditions. On the basis of the emission energy trend, the excited state of these luminescent bioconjugates is likely to bear a high parentage of (3)MLCT (dpi(Ir)-->pi*(N-N)) character. In addition, the glycoprotein avidin (Av) has also been conjugated with complexes 1-4 to give the bioconjugates 1-Av-4-Av. Upon photoexcitation, these bioconjugates also display intense and long-lived (3)MLCT (dpi(Ir)-->pi*(N-N)) emission in aqueous buffer at 298 K. Furthermore, a heterogeneous competitive assay for biotin has been developed using 2-Av and biotinylated microspheres. We have shown that complexes 1-4 represent a new class of multicolor luminescent cross-linkers for biomolecular species.
我们报道了一系列含有两个醛官能团的发光环金属化铱(III)配合物Ir(pba)(2)(N-N)(Hpba = 4-(2-吡啶基)苯甲醛;N-N = 2,2'-联吡啶,bpy (1),1,10-菲咯啉,phen (2),3,4,7,8-四甲基-1,10-菲咯啉,3,4,7,8-Me(4)-phen (3),4,7-二苯基-1,10-菲咯啉,4,7-Ph(2)-phen (4))的合成、表征、光物理和电化学性质。研究了配合物1的X射线晶体结构。光激发后,配合物1 - 4在298 K的流体溶液和低温玻璃中表现出强烈且长寿命的发射。发光归因于与pba(-)配体相关的三重态配体内((3)IL)激发态,可能混合了一些三重态金属到配体的电荷转移((3)MLCT)(dpi(Ir)-->pi*(pba(-)))特征。由于这些配合物中的每一个都具有两个醛基,在还原胺化后可以与生物分子的伯胺基团反应形成稳定的仲胺,我们研究了这些配合物作为生物底物新型发光交联剂的可能性。L-丙氨酸已用配合物1 - 4进行标记,得到发光生物共轭物1-(Ala)(2)-4-(Ala)(2)。这些共轭物在环境条件下显示出强烈的光致发光和长发射寿命。基于发射能量趋势,这些发光生物共轭物的激发态可能具有高比例的(###)MLCT(dpi(Ir)-->pi*(N-N))特征。此外,糖蛋白抗生物素蛋白(Av)也已与配合物1 - 4共轭,得到生物共轭物1-Av-4-Av。光激发后,这些生物共轭物在298 K的水性缓冲液中也显示出强烈且长寿命的(###)MLCT(dpi(Ir)-->pi*(N-N))发射。此外,使用2-Av和生物素化微球开发了一种针对生物素的异质竞争分析方法。我们已经表明,配合物1 - 4代表了一类用于生物分子物种的新型多色发光交联剂。