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Journal ArticleDOI

Solid Eu(III) complexes studied by positron annihilation, optical and Mössbauer spectroscopies: insights on the positronium formation mechanism.

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TLDR
Strong evidences that the electronic delocalization does not occur at both temperatures are found and suggest that the absence of positronium in Eu(III) complexes cannot be explained by a ligand/metal charge transfer process.
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This article is published in Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy.The article was published on 2012-06-15. It has received 15 citations till now. The article focuses on the topics: Positronium.

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Citations
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Journal ArticleDOI

The Role of the Ligand-to-Metal Charge-Transfer State in the Dipivaloylmethanate-Lanthanide Intramolecular Energy Transfer Process

TL;DR: In this paper, the photoluminescent properties of the monomeric and dimeric complexes are dependent on the energy positions of the low-lying ligand-to-metal charge transfer (LMCT) state, which may be correlated with the chelating and chelate bridging coordination modes of the dpm ligand.
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Synthesis of amino acid iodine charge transfer complexes in situ methanolic medium: Chemical and physical investigations

TL;DR: In this article, a new procedure for preparation of glycine and alanine triiodide charge transfer complexes by solid-solid interactions using different spectroscopic tools was investigated, which revealed that most of PAL and PADB parameters are strongly correlated with the molecular weight of the prepared CT complexes.
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Evidence of the participation of electronic excited states in the mechanism of positronium formation in substitutional Tb1−xEux(dpm)3 solid solutions studied by optical and positron annihilation spectroscopies

TL;DR: A strong linear correlation between the (5)D(4) Tb(iii) energy level excited state lifetime and the positronium formation probability has been observed, indicating that the ligand-to-metal charge transfer LMCT states act in both luminescence quenching and positronia formation inhibition, as previously proposed.
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Coordination Geometrical Effect on Ligand-to-Metal Charge Transfer-Dependent Energy Transfer Processes of Luminescent Eu(III) Complexes

TL;DR: In this paper, the LMCT-dependent energy transfer processes of seven and eight-coordinated europium (Eu(III) ion were demonstrated for the first time using temperature-dependent and time-resolved emission lifetime measurements of 5D0 → 7FJ transitions of Eu (III) ions.
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Luminescence and positron spectroscopies studies of tris(2,2,6,6-tetramethyl-3,5-heptanedionate) europium(III) and terbium(III) complexes containing 2-pyrrolidone as coligand

TL;DR: In this paper, the synthesis, characterization, luminescent properties and positronium formation yields of europium and terbium(III) complexes of stoichiometric formula Ln(dpm)3(2-pyr), where: Ln = Eu and Tb, dpm = 2,2,6,6-tetramethyl-3,5-heptanedionato (dipivaloylmethanate) ion, a β-diketonate ligand, and 2 pyr = γ-l
References
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Journal ArticleDOI

Spectroscopic properties and design of highly luminescent lanthanide coordination complexes

TL;DR: In this paper, the development of efficient light conversion molecular devices (LCMDs) based on lanthanide complexes is reviewed, with emphasis on the work of our group, who have adopted a strategy based upon both theoretical and experimental (synthesis and methodological) investigations.
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Positronfit Extended: A New Version of a Program for Analysing Positron Lifetime Spectra

TL;DR: The POSITRONFIT EXTENDED extended version of this program is available from the CPC Program Library, Queen's Uni, Toronto, Ontario, Canada, Canada.
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Spur reaction model of positronium formation

TL;DR: In this article, a new model of positronium (Ps) formation is proposed, which is based on a reaction between a positron and an electron in the positron spur.
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Observation of electron hopping in 151Eu3S4 by Mössbauer spectroscopy

TL;DR: In this paper, an electron hopping model together with an exchange narrowing formula yield a temperature dependent hopping time characteristic of an activation process, and the activation energy found is 0.24 eV.
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