Step-wise changes in the excited state lifetime of [Eu(DO)] and [Eu(DOTA)(DO)] as a function of the number of inner-sphere O-H oscillators.

Lanthanide luminescence is dominated by quenching by high-energy oscillators in the chemical environment. The rate of non-radiative energy transfer to a single HO molecule coordinated to a Eu ion exceeds the usual rates of emission by an order of magnitude. We know these rates, but the details of these energy transfer processes are yet to be established.

Mapping the distribution of electronic states within the D and F levels of Tb complexes with optical spectroscopy.

The Tb(III) ion has the most intense luminescence of the trivalent lanthanide(III) ions. In contrast to Eu(III), where the two levels only include a single state, the high number of electronic states in the ground (F) and emitting (D) levels makes detailed interpretations of the electronic structure-the crystal field-difficult. Here, luminescence emission and excitation spectra of Tb(III) complexes with 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA, [Tb(DOTA)(HO)]), ethylenediaminetetraacetic acid (EDTA, [Tb(EDTA)(HO)]) and diethylenetriaminepentaacetic acid (DTPA, [Tb(DTPA)(HO)]) as well as the Tb(III) aqua ion ([Tb(HO)]) were recorded at room temperature and in frozen solution.

Synthesis and Properties of Fluorenone-Containing Cycloparaphenylenes and Their Late-Stage Transformation.

Cycloparaphenylenes (CPPs) are the smallest possible armchair carbon nanotubes, the properties of which strongly depend on their ring size. They can be further tuned by either peripheral functionalization or by replacing phenylene rings for other aromatic units. Here we show how four novel donor-acceptor chromophores were obtained by incorporating fluorenone or 2-(9H-fluoren-9-ylidene)malononitrile into the loops of two differently sized CPPs.

Tb Photophysics: Mapping Excited State Dynamics of [Tb(HO)] Using Molecular Photophysics.

The study of optical transitions in lanthanide(III) ions has evolved separately from molecular photophysics, but the framework still applies to these forbidden transitions. In this study, a detailed photophysical characterization of the [Tb(HO)] aqua ion was performed. The luminescence quantum yield (Φ), excited state lifetime (τ), radiative ( ≡ ) and nonradiative () rate constants, and oscillator strength () were determined for Tb(CFSO) in HO/DO mixtures in order to map the radiative and nonradiative transition probabilities.

Electronic Materials: An Antiaromatic Propeller Made from the Four-Fold Fusion of Tetraoxa[8]circulene and Perylene Diimides.

The synthesis of an antiaromatic tetraoxa[8]circulene annulated with four perylene diimides (PDI), giving a dynamic non-planar π-conjugated system, is described. The molecule contains 32 aromatic rings surrounding one formally antiaromatic planarized cyclooctatetraene (COT). The intense absorption (ϵ=3.

Revisiting the assignment of innocent and non-innocent counterions in lanthanide(III) solution chemistry.

Lanthanides are found in critical applications from display technology to renewable energy. Often, these rare earth elements are used as alloys or functional materials, yet access to them is through solution processes. In aqueous solutions, the rare earths are found predominantly as trivalent ions and charge balance dictates that counterions are present.

: Investigating [Eu(HO)] Photophysics and Creating a Method to Bypass Luminescence Quantum Yield Determinations.

Lanthanide luminescence has been treated separate from molecular photophysics, although the underlying phenomena are the same. As the optical transitions observed in the trivalent lanthanide ions are forbidden, they do belong to the group that molecular photophysics has yet to conquer, yet the experimental descriptors remain valid. Herein, the luminescence quantum yields (ϕ), luminescence lifetimes (τ), oscillator strengths (), and the rates of nonradiative () and radiative ( ≡ ) deactivation of [Eu(HO)] were determined.

Temperature Dependence of Fundamental Photophysical Properties of [Eu(MeOH-)] Solvates and [Eu·DOTA(MeOH-)] Complexes.

The trivalent lanthanide ions show optical transitions between energy levels within the 4f shell. All these transitions are formally forbidden according to the quantum mechanical selection rules used in molecular photophysics. Nevertheless, highly luminescent complexes can be achieved, and terbium(III) and europium(III) ions are particularly efficient emitters.

Electronic Structure of Ytterbium(III) Solvates-a Combined Spectroscopic and Theoretical Study.

The wide range of optical and magnetic properties of lanthanide(III) ions is associated with their intricate electronic structures which, in contrast to lighter elements, is characterized by strong relativistic effects and spin-orbit coupling. Nevertheless, computational methods are now capable of describing the ladder of electronic energy levels of the simpler trivalent lanthanide ions, as well as the lowest energy term of most of the series. The electronic energy levels result from electron configurations that are first split by spin-orbit coupling into groups of energy levels denoted by the corresponding Russell-Saunders terms.

The effect of weighted averages when determining the speciation and structure-property relationships of europium(iii) dipicolinate complexes.

Lanthanide(iii) coordination chemistry in solution is inherently complicated by the lack of directional interactions and rapid ligand exchange. The latter can be eliminated in kinetically inert complexes, but remains a challenge in complexes between lanthanide(iii) ions and smaller ligands. As multiple conformations and partial decomplexation is an issue even with multidentate ligands, it will influence the observed solution properties of complexes of smaller ligands common in the field of f-elements coordination chemistry such as acetylacetonates and dipicolinates.

Solution Structure, Electronic Energy Levels, and Photophysical Properties of [Eu(MeOH)(NO)] Complexes.

The structure of lanthanide(III) ions in solutions high in nitrate has been debated since the early days of lanthanide coordination chemistry. The structure and properties of lanthanides in these solutions are essential in industrial rare-earth separation, as well as in the fundamental solution chemistry of these elements. Pending decades of debate, it was established that nitrate is bidentate and coordinates in the inner sphere, and complexes have been observed with as many as four nitrates coordinated to a single lanthanide(III) center in nonaqueous solutions.

π-Expanded Thioxanthones - Engineering the Triplet Level of Thioxanthone Sensitizers for Lanthanide-Based Luminescent Probes with Visible Excitation.

Bright lanthanide based probes for optical bioimaging must rely on the antenna principle, where the lanthanide-centred excited state is formed by a complex sensitization process. Efficient sensitization of lanthanide-centred emission occurs via triplet states centred on the sensitizing chromophore. Here, the triplet state of thioxanthone chromophores is modulated by extending the π-system.

π-Expanded Thioxanthones-Engineering the Triplet Level of Thioxanthone Sensitizers for Lanthanide-Based Luminescent Probes with Visible Excitation.

Invited for this month's cover are the collaborating groups of Dr. Thomas Just Sørensen at the University of Copenhagen, Denmark and Dr. Robert Pal at Durham University, United Kingdom.

Electronic Energy Levels of Dysprosium(III) ions in Solution. Assigning the Emitting State and the Intraconfigurational 4f-4f Transitions in the Vis-NIR Region and Photophysical Characterization of Dy(III) in Water, Methanol, and Dimethyl Sulfoxide.

Dysprosium(III) ions are the third most luminescent lanthanide(III) ions. Dy(III) is used as dopant in optical fibers and as shift reagent in NMR imaging and is the element at the forefront of research in single-molecule magnets. Nonetheless, the excited state manifold of the dysprosium(III) ion is not fully mapped and the nature of the emitting state has not been unequivocally assigned.