分子内力
发光
化学
异核分子
共振(粒子物理)
质子化
激发态
离子
氢键
乙二胺
光化学
荧光
结晶学
无机化学
立体化学
核磁共振波谱
分子
材料科学
有机化学
物理
光电子学
粒子物理学
量子力学
核物理学
作者
Olena Trunova,Н. В. Русакова
出处
期刊:Ukraïnsʹkij hìmìčnij žurnal
[V.I. Vernadsky Institute of General and Inorganic Chemistry]
日期:2023-07-28
卷期号:89 (6): 55-70
标识
DOI:10.33609/2708-129x.89.06.2023.55-70
摘要
An analysis of the fluorescent characteristics of ethylenediamine-N,N'-disuccinic and N,N-bis(phosphonomethyl)-2-aminopropionic acids was carried out depending on the pH of the solutions. It was established that the change in fluorescence intensity and lifetime is associated with the formation of variously protonated forms of acids in which stable H-cycles are formed with the participation of hydrogen bonds. The energies of the singlet and triplet levels of the ligands were experimentally determined, the values of which are higher than the energy of the radiative level of the Nd(III) ion, which indicates the possibility of intramolecular transfer of the excitation energy to the resonance level of the lanthanide ion. It was established that both homo- and heteronuclear complexes of Nd(III) exhibit 4f-luminescence in the near-IR region. It was found that for phosphorus-containing complexes there is an increase in luminescence intensity and relative quantum yields in comparison with aminocarboxylate analogs. In heterometallic complexes based on aminopolycarboxylic acids, the intramolecular transfer of energy from the excited level of Co(II) to the resonance level of the f-metal leads to sensitization of the 4f-luminescence of the neodymium ion.
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