2003
DOI: 10.1016/s0925-8388(02)01118-0
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Synthesis and luminescence of a novel conjugated europium complex with 6-paramethylaniline carbonyl 2-pyridine carboxylate

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Cited by 13 publications
(12 citation statements)
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“…Now days, organic luminescent materials are used commercially for examples in lap-top computers, mobile phones, car dashboards, advertisement panels, decorating lighting, etc. Some organic ligands efficiently sensitize Eu +3 luminescence but not Tb +3 at room temperature [17,23,24]. We proposed the new organic ligand 2 0 -hydroxy-4 0 ,6 0 -dimethoxyacetophenone keeping in view that this is found to sensitize Eu +3 as well as Tb +3 luminescence excellently.…”
Section: Introductionmentioning
confidence: 94%
“…Now days, organic luminescent materials are used commercially for examples in lap-top computers, mobile phones, car dashboards, advertisement panels, decorating lighting, etc. Some organic ligands efficiently sensitize Eu +3 luminescence but not Tb +3 at room temperature [17,23,24]. We proposed the new organic ligand 2 0 -hydroxy-4 0 ,6 0 -dimethoxyacetophenone keeping in view that this is found to sensitize Eu +3 as well as Tb +3 luminescence excellently.…”
Section: Introductionmentioning
confidence: 94%
“…These two bonds are obviously weakened in the NPs compared with those in the ligand. This can be attributed to the rigid structure of the coordinated complex, which restricts stretching or bending of the C==O and N-H groups [32]. peak ( Figure 5(b)).…”
Section: 1mentioning
confidence: 99%
“…[22]), at room temperature. Table 2 shows that the luminescence lifetimes of the emitting 5 D 0 level for the complexes obtained are longer than that reported for the Eu(TTA) 3 4 Phen 2 is mainly ascribed to the formation of polynuclear structure of the complex, which results in a rigid polymeric chain structure.…”
Section: Article In Pressmentioning
confidence: 99%