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J Sokolnicki

Publications and source records attributed to J Sokolnicki.

At least 19 recordsLinked to original sources

Characterization of the electronic excited-state energetics and solution structure of lanthanide(III) complexes with the polypyridine ligand 6,6'-bis[bis(2-pyridylmethyl)aminomethyl]-2,2'-bipyridine.

Absorption, emission, and excitation spectra for solid-state and solution of Tb(III), Dy(III), and Gd(III) complexes with the polypyridine ligand 6,6'-bis[bis(2-pyridylmethyl)-aminomethyl]-2,2'-bipyridine (C36H34N8) are presented. Measurements of excited-state lifetimes and quantum yields in various solvents at room temperature and 77 K are also reported and used to characterize the excited-state energetics of this system. Special attention is given to the characterization of metal-to-ligand energy transfer efficiency and mechanisms. The measurement of circularly polarized luminescence (CPL) from the solution of the Dy(III) complex following circularly polarized excitation confirms the chiral structure of the complexes under study. No CPL is present in the luminescence from the Eu(III) or Tb(III) complex because of efficient racemization. The variation of the magnitude of the CPL as a function of temperature from an aqueous solution of DyL is used for the first time to characterize the solution equilibria between different chiral species.

2,2'-Dipyridyl↗

Effect of ligand radicals on vibrational IR, Raman and vibronic spectra of europium beta-diketonates.

Vibrational IR, Raman spectra and vibronic sidebands of Eu(3+) electronic transitions of europium tris-beta-diketonates Eu(beta)(3).Ph (beta-dipyvaloylmethane (DPM), acetylacetone (AA), benzoylacetone (BA), thenoyltrifluoroacetone (TTFA) and other beta-diketones; Ph-methyl-, phenyl-, and nitro-derivatives of 1,10-phenanthroline (Phen)) as well as Eu(beta)(3).Bpy and Eu(beta)(3).D-Bpy (Bpy- and D-Bpy-H- and D-2,2'-bipyridine) were studied. Effect of ligand radical properties on spectra and manifestation of the reciprocal influence of non-equivalent ligands in spectra are discussed. Dependence of the spectra on electronic density distribution in both ligands as well as on the strength of M-O and M-N bonds at the variation of radicals of one of the ligands, beta or Ph, was examined. Shape of vibronic sidebands was analysed. Behaviour of bands in the middle and far regions of IR spectra of the series Eu(beta)(3).Phen and Eu(TTFA)(3).Ph was investigated. Increase of the polarising influence of Eu(3+) ions on Phen and Bpy molecules and strengthening the Eu-N bonds in TTFA compounds in comparison with DPM compounds were disclosed from the Raman spectra of Eu(beta)(3).Phen and Eu(beta)(3).Bpy, that is in accordance with properties of beta-diketone radicals. Conclusion about weaker Eu-N bonds in europium beta-diketonates with heterocyclic diimines in comparison with corresponding nitrates was derived from the spectra. Spectral data concerning the relative strength of Eu-ligand bonds are in agreement with available X-ray data.

Europium↗