Journal
CHEMISTRY LETTERS
Volume 50, Issue 7, Pages 1382-1384Publisher
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.210150
Keywords
Ln luminescence; Tripodal Schiff base; Coordination environment
Categories
Funding
- Japan Society for the Promotion of Science (JSPS) KAKENHI [20K15308]
- Grants-in-Aid for Scientific Research [20K15308] Funding Source: KAKEN
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The Ln(III)-tripodal Schiff base complex (TbLtrpn)-L-III was prepared, with the three arms of the ligand extended by one methylene compared to (TbLtren)-L-III. The enhanced TbIII-centered luminescence in (TbLtrpn)-L-III was attributed to the diminished symmetry of the seven-coordination environment of the Tb-III center, leading to an increased radiative transition rate. This provides a new insight for improving the luminescence properties of lanthanide metal complexes.
Ln(III)-tripodal Schiff base complex (TbLtrpn)-L-III was prepared, in which the three arms of the ligand were extended by one methylene based on the tris(2-aminoethyl)amine in (TbLtren)-L-III. (TbLtrpn)-L-III showed enhanced TbIII-centered luminescence compared to TbIIILtren. Crystallographic analysis revealed that the symmetry of the seven-coordination environment of the Tb-III center in (TbLtrpn)-L-III was diminished compared to that in (TbLtren)-L-III, resulting in the increased radiative transition rate and/or decreased back energy transfer rate and, thus, the increased luminescence.
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