4.8 Article

Thermally Activated Photophysical Processes of Organolanthanide Complexes in Solution

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 13, Issue 21, Pages 4800-4806

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.2c01350

Keywords

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Funding

  1. Hong Kong Research Grants Council [12300021]
  2. Centre for Medical Engineering of Molecular and Biological Probes [AoE/M-401/20]
  3. Dr. Mok Man Hung Endowed Professorship in Chemistry, HKBU-Durham Lanthanide Joint Research Center - Lanthanide Tools for Systems Medicine [SDF19-1011-P02]

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The effect of temperature on the luminescence lifetime and intensity of lanthanide complexes in toluene solution was studied, revealing different behaviors among various lanthanide elements at different temperatures.
The effect of temperature upon the lanthanide luminescence lifetime and intensity has been investigated in toluene solution for the complexes LnPhen(TTA)(3) (Ln = Eu, Sm, Nd, Yb; Phen = 1,10-phenanthroline; TTA = thenoyltrifluoroacetonate). Thermally excited back-transfer to a charge transfer state was found to occur for Ln = Eu and can be explained by lifetime and intensity back-transfer models. The emission intensity and lifetime were also quenched with increasing temperature for Ln = Sm, and the activation energy for nonradiative decay is similar to that for the thermal population of Sm3+ excited states. Unusual behavior for lifetime and intensity was found for both Ln = Nd, Yb. The usually assumed equivalence of tau/tau(0) = I/I-0 (where tau is lifetime and I is intensity) does not hold for these cases. We infer that for these lanthanide systems the intensity decreases with temperature in the stage prior to population of the luminescent state. The lifetime changes are discussed.

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