Nonat Aline, Imbert Daniel, Pécaut Jacques, Giraud Marion, Mazzanti Marinella
Laboratoire de Reconnaissance Ionique et Chimie de Coordination, Service de Chimie Inorganique et Biologique (UMR-E 3 CEA-UJF), INAC, CEA-Grenoble, 38054 Grenoble Cedex 09, France.
Inorg Chem. 2009 May 4;48(9):4207-18. doi: 10.1021/ic9000076.
The tripodal H(3)thqtcn ligand allows the synthesis of well-defined neutral monomeric syn-tris(hydroxyquinolinate) complexes of lanthanides. Pure [Ln(thqtcn)] complexes (Ln = Nd, 1; Er, 2; Yb, 3) of the triply deprotonated ligand thqtcn(3-) were prepared. Crystallographic characterization was carried out for complexes 1 and 3, showing that the ligand is flexible enough to wrap around Ln(III) of different size with a tricapped trigonal-prism coordination geometry. The partially protonated H(1.5)thqtcn(1.5-) ligand also binds strongly to Ln(III) ions in methanol and water (at pH approximately 5). The X-ray diffraction study shows that protonated complexes crystallize as chiral dimers of formula Ln(H(1.5)thqtcn)(OTf)(3) x 3 MeOH (Ln = Nd, 4; Yb, 5) in which two equivalent monomeric complexes of the partially protonated H(1.5)thqtcn(1.5-) are bridged by very strong hydrogen bonds between the phenol oxygen atoms. The ligand thqtcn(3-) sensitizes efficiently the near-infrared emission of Er, Nd (0.10% Qy), and Yb (0.60% Qy). For the first time, the effect of ligand protonation on the efficiency of the solid-state luminescence emission of lanthanides complexes is demonstrated by the decrease of the luminescence quantum yield observed for Yb(H(1.5)thqtcn)(OTf)(3) (0.26%) with respect to [Yb(thqtcn)] (0.60%). The water-soluble H(3)thqtcn-SO(3) analogue of H(3)thqtcn and its lanthanide complexes has been prepared. The solution quantum yields of the thqtcn-SO(3)(3-) complexes were measured in water at pH 7.4 (0.016% for Nd(III) and 0.14% for Yb(III)) and in deuterated water (Nd, 0.047%; Yb, 0.55%), and they are among the highest reported in the literature for Yb(III) in aqueous solutions. The high thermodynamic and kinetic stability in water at physiological pH of the gadolinium complex of thqtcn-SO(3)(3-) indicate that the lanthanide complexes of thqtcn(3-) and thqtcn-SO(3)(3-) are highly resistant to hydrolysis and therefore are well suited for the development of luminescent devices and for application as probes in biomedical imaging.
三脚架状的H(3)thqtcn配体可用于合成结构明确的镧系元素中性单体顺式三(羟基喹啉酸酯)配合物。制备了三去质子化配体thqtcn(3-)的纯[Ln(thqtcn)]配合物(Ln = Nd,1;Er,2;Yb,3)。对配合物1和3进行了晶体学表征,结果表明该配体具有足够的柔韧性,能够以三帽三角棱柱配位几何结构围绕不同尺寸的Ln(III)。部分质子化的H(1.5)thqtcn(1.5-)配体在甲醇和水中(pH约为5)也能与Ln(III)离子强烈结合。X射线衍射研究表明,质子化配合物以式Ln(H(1.5)thqtcn)(OTf)(3)·3MeOH(Ln = Nd,4;Yb,5)的手性二聚体形式结晶,其中两个部分质子化的H(1.5)thqtcn(1.5-)的等效单体配合物通过酚氧原子之间非常强的氢键桥连。配体thqtcn(3-)能有效敏化Er、Nd(0.10%量子产率)和Yb(0.60%量子产率)的近红外发射。首次通过观察到的Yb(H(1.5)thqtcn)(OTf)(3)(0.26%)相对于[Yb(thqtcn)](0.60%)的发光量子产率降低,证明了配体质子化对镧系元素配合物固态发光发射效率的影响。制备了H(3)thqtcn的水溶性H(3)thqtcn-SO(3)类似物及其镧系元素配合物。thqtcn-SO(3)(3-)配合物在pH 7.4的水中(Nd(III)为0.016%,Yb(III)为0.14%)和氘代水中(Nd为0.047%;Yb为0.55%)的溶液量子产率进行了测定,它们是文献中报道的Yb(III)在水溶液中的最高值之一。thqtcn-SO(3)(3-)的钆配合物在生理pH的水中具有高的热力学和动力学稳定性,这表明thqtcn(3-)和thqtcn-SO(3)(3-)的镧系元素配合物对水解具有高度抗性,因此非常适合用于发光器件的开发以及作为生物医学成像中的探针应用。