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Luminescent Ruthenium(ll)Bipyridine-Calix[4]arene Complexes as Receptors for Lanthanide Cations

机译:发光钌(II)联吡啶-Calix [4]芳烃配合物作为镧系阳离子的受体

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摘要

The synthesis and photophysical properties of novel luminescent ruthenium(II)bipyridyl complexes containing one,two,or six lower rim acid-amide-modified calix[4]arene moieties covalently linked to the bipyridine groups are reported which are designed to coordinate and sense luminescent lanthanide ions.All the Ru-calixarene complexes synthesized in this work are able to coordinate Nd~(3+),Eu~(3+),and Tb~(3+)ions with formation of adducts of variable stoichiometry.The absorbance changes allow the evaluation of association constants whose magnitudes depend on the nature of the complexes as well as on the nature of the lanthanide cation.Lanthanide cation complex formation affects the ruthenium luminescence which is strongly quenched by Nd~(3+)ion,moderately quenched by the Eu~(3+)ion,and poorly or moderately increased by the Tb~(3+)ion.In the case of Nd~(3+),the excitation spectra show that(i)the quenching of the Ru luminescence occurs via energy transfer and(ii)the electronic energy of the excited calixarene is not transferred to the Ru(bpy)_3 but to the neodymium cation.In the case of Tb~(3+),the adduct's formation leads to an increase of the emission intensities and lifetimes.The reason for this behavior was ascribed to the electric field created around the Ru calix[4]arene complexes by the Tb~(3+)ions by comparison with the Gd~(3+)ion,which behaves identically and can affect ruthenium luminescence only by its charge.However,especially for compounds 1 and 3,it cannot be excluded that some contribution comes from the decrease of vibrational motions(and nonradiative processes)due to the rigidification of the structure upon Tb~(3+)complexation.In the case of Eu~(3+),compounds 1,2,and 4 were quenched by the lanthanide addition but the quenching of the ruthenium luminescence is not accompanied by europium-sensitized emission which suggests that an electron-transfer mechanism is responsible for the quenching.On the contrary,compound 3 exhibits enhanced emission upon addition of Eu3+(as nitrate salt);it is suggested that the lack of quenching in the[3-2Eu~3+]adduct is due to kinetic reasons because the electron-transfer quenching process is thermodynamically allowed.
机译:报告了新型发光钌(II)联吡啶配合物的合成和光物理性质,该配合物包含与联吡啶基共价连接的一个,两个或六个低级酸酰胺改性的杯[4]芳烃部分,用于协调和感应发光这项工作中合成的所有Ru-杯芳烃配合物都能够与Nd〜(3 +),Eu〜(3+)和Tb〜(3+)离子配位并形成化学计量比可变的加合物。允许评估缔合常数,缔合常数的大小取决于配合物的性质以及镧系元素阳离子的性质。镧系元素阳离子配合物的形成会影响钌的发光,该发光被Nd〜(3+)离子强烈淬灭,而被Nd〜(3+)离子淬灭Eu〜(3+)离子,并由Tb〜(3+)离子弱或中等增加。在Nd〜(3+)的情况下,激发光谱表明(i)发生Ru发光的猝灭通过能量转移和(ii)的电子能量激发的杯芳烃不转移到Ru(bpy)_3上,而是转移到钕阳离子上。在Tb〜(3+)的情况下,加合物的形成导致发射强度和寿命的增加,其原因是归因于Tb〜(3+)离子与Gd〜(3+)离子相比,Ru杯[4]芳烃络合物在Ru杯[4]芳烃配合物周围产生的电场,其行为相同,仅通过电荷就能影响钌的发光。尤其是对于化合物1和3而言,不能排除由于Tb〜(3+)络合过程中结构的刚性而导致的振动运动(和非辐射过程)的减少所带来的某些贡献。 3+),化合物1,2和4通过镧系元素的加入淬灭,但钌发光的淬灭并没有伴随euro敏感的发射,这表明电子传递机制是造成淬灭的原因。化合物3加成后发射增强Eu 3+(以硝酸盐的形式);建议[3-2Eu〜3 +]加合物没有淬灭是由于动力学原因,因为电子传递淬灭过程是热力学上允许的。

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