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Monoporphyrinate neodymium (III) complexes stabilized by tripodal ligand: synthesis, characterization and luminescence

机译:三脚架配体稳定的单卟啉钕(III)配合物:合成,表征和发光

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A series of monoporphyrinate neodymium (III) complexes stabilized by anionic tripodal ligand (cyclopentadienyl)tris(dimethyl-phosphito)cobaltate(I) were prepared and characterized by IR, ESI-HRMS, UV-Vis and X-ray diffraction studies. Structural analyses revealed that the Nd3+ ion was seven-coordinate, surrounded by four nitrogen atoms from the porphyrinate dianion and three oxygen atoms from the anionic tripodal ligand. Photoluminescence studies showed that the porphyrinate dianion acting as a sensitizer absorbed the light and transferred the energy to the Nd3+ center, which then allowed the metal ion to emit efficiently at 885 and 1071 nm. The luminescent intensity of the complexes increases when there are strong electronic donating groups on the porphyrin rings but decreases with increasing polarity of the solvents. (C) 2004 Elsevier B.V. All rights reserved.
机译:制备了一系列由阴离子三脚架配体(环戊二烯基)三(二甲基-磷酸)钴(I)稳定的单卟啉钕(III)配合物,并通过IR,ESI-HRMS,UV-Vis和X射线衍射研究对其进行了表征。结构分析表明,Nd3 +离子为七配位,被卟啉双阴离子的四个氮原子和阴离子三脚架配体的三个氧原子包围。光致发光研究表明,作为敏化剂的卟啉二价阴离子吸收光并将能量转移到Nd3 +中心,然后使金属离子在885和1071 nm处有效发射。当在卟啉环上有强的供电子基团时,配合物的发光强度增加,但随着溶剂极性的增加而降低。 (C)2004 Elsevier B.V.保留所有权利。

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