Ahmed Toushique, Chakraborty Amit, Paul Animesh, Baitalik Sujoy
Inorganic Chemistry Section, Department of Chemistry, Jadavpur University, Kolkata 700032, India.
Dalton Trans. 2023 Oct 10;52(39):14027-14038. doi: 10.1039/d3dt01701j.
We designed four ternary lanthanide tris-(β-diketonate) complexes of the form [Ln(tta)(tpy-HImzphen)], where Ln = La, Eu, Sm and Tb; tta = (2-theonyltrifluoroacetonate) and tpy-HImzphen = 2-(4-[2,2':6',2'']terpyridin-4'-yl-phenyl)-1-phenanthro[9,10-]imidazole. All the complexes have been thoroughly characterized by standard analytical tools and spectroscopic techniques including single crystal X-ray diffraction. generation of the complexes was also monitored absorption and emission spectroscopy upon incremental addition of the respective lanthanide precursor {Ln(tta)(HO)} to the dichloromethane solution of the terpyridyl-imidazole ligand. The photophysical behaviors of all the complexes were thoroughly investigated absorption and both steady-state and time-resolved emission spectroscopic techniques. The emission spectral measurements were carried out at both room temperature and 77 K to understand the deactivation dynamics of the excited states and elucidate the distinctive luminescence responses from the four lanthanide metal ions owing to the introduction of the terpyridyl-based ancillary ligand.
我们设计了四种通式为[Ln(tta)(tpy-HImzphen)]的三元镧系三(β-二酮)配合物,其中Ln = La、Eu、Sm和Tb;tta = (2-噻吩甲酰三氟丙酮),tpy-HImzphen = 2-(4-[2,2':6',2'']-三联吡啶-4'-基-苯基)-1-菲并[9,10-]咪唑。所有配合物均已通过标准分析工具和光谱技术进行了全面表征,包括单晶X射线衍射。在向三联吡啶-咪唑配体的二氯甲烷溶液中逐步添加相应的镧系前驱体{Ln(tta)(HO)}时还通过吸收和发射光谱监测了配合物的生成。利用吸收光谱以及稳态和时间分辨发射光谱技术对所有配合物的光物理行为进行了全面研究。在室温及77 K下进行发射光谱测量,以了解激发态的失活动力学,并阐明由于引入基于三联吡啶的辅助配体而导致的四种镧系金属离子独特的发光响应。