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      Thermally Activated Photophysical Processes of Organolanthanide Complexes in Solution

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          Abstract

          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 Sm 3+ excited states. Unusual behavior for lifetime and intensity was found for both Ln = Nd, Yb. The usually assumed equivalence of τ/τ 0 = I/ I 0 (where τ 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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            A luminescent mixed-lanthanide metal-organic framework thermometer.

            A luminescent mixed lanthanide metal-organic framework approach has been realized to explore luminescent thermometers. The targeted self-referencing luminescent thermometer Eu(0.0069)Tb(0.9931)-DMBDC (DMBDC = 2, 5-dimethoxy-1, 4-benzenedicarboxylate) based on two emissions of Tb(3+) at 545 nm and Eu(3+) at 613 nm is not only more robust, reliable, and instantaneous but also has higher sensitivity than the parent MOF Tb-DMBDC based on one emission at a wide range from 10 to 300 K. © 2012 American Chemical Society
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              Lanthanide Nanoparticles: From Design toward Bioimaging and Therapy.

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                Author and article information

                Journal
                J Phys Chem Lett
                J Phys Chem Lett
                jz
                jpclcd
                The Journal of Physical Chemistry Letters
                American Chemical Society
                1948-7185
                26 May 2022
                02 June 2022
                : 13
                : 21
                : 4800-4806
                Affiliations
                []Department of Chemistry, Hong Kong Baptist University , Waterloo Road, Kowloon Tong, Hong Kong S.A.R., P. R. China
                []State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, Key Laboratory of Oil and Gas Fine Chemicals, Ministry of Education & Xinjiang Uygur Autonomous Region, Urumqi Key Laboratory of Green Catalysis and Synthesis Technology, College of Chemistry, Xinjiang University , Urumqi 830046, Xinjiang, P. R. China
                Author notes
                Author information
                https://orcid.org/0000-0002-4366-9113
                https://orcid.org/0000-0001-9960-7467
                https://orcid.org/0000-0002-7740-9408
                https://orcid.org/0000-0002-3750-5980
                https://orcid.org/0000-0002-4681-6203
                Article
                10.1021/acs.jpclett.2c01350
                9169037
                35616284
                9e0643f9-cb0b-46bd-a7fb-ceacaab89ce4
                © 2022 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 05 May 2022
                : 24 May 2022
                Funding
                Funded by: Research Grants Council, University Grants Committee, doi 10.13039/501100002920;
                Award ID: 12300021
                Funded by: HKBU-Durham Lanthanide Joint Research Center – Lanthanide Tools for Systems Medicine, doi NA;
                Award ID: SDF19-1011-P02
                Funded by: Centre for Medical Engineering of Molecular and Biological Probes, doi NA;
                Award ID: AoE/M-401/20
                Categories
                Letter
                Custom metadata
                jz2c01350
                jz2c01350

                Physical chemistry
                Physical chemistry

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