LuBO3 crystallizes in the calcite type (CaCO3) structure and is a widely applied inorganic host for luminescent materials and scintillators. Even though many scientific works have been published concerning the optical properties of rare earth doped LuBO3, so far, no study of the emission spectra as function of the excitation energy of such orthoborates has been conducted. Therefore, this work deals with the photoluminescence of RE doped LuBO3 with RE = Ce3+, Eu3+, Gd3+, or Tb3+, while an emphasize is laid on the energy dependence of these four luminescent compounds.

TmMgB5O10 spontaneous crystals were synthesized via flux-growth technique from a K2Mo3O10-based solvent. The crystal structure of the compound was solved and refined within the space group P21/n. The first principles calculations of the electronic structure reveal that TmMg-pentaborate is an insulator with an indirect energy band gap of approximately 6.37 eV. Differential scanning calorimetry measurements and powder X-ray diffraction studies of heat-treated solids show that TmMgB5O10 is an incongruent melting compound. A characteristic band of Tm3+ cation corresponding to the 3H6 → 1D2 transition is observed in the photoluminescence excitation spectra of TmMg-borate. The as-obtained crystals exhibit intense blue emission with the emission peaks centered at 455, 479, 667 and 753 nm. The most intensive band corresponds to the 1D2 3F4 transition.

In spite of large-scale investigations of homogeneous single-site metallocene catalysts and systems based on them, the problem of controlling their activity, chemo- and stereoselectivity with the aim of developing efficient methods for the preparation of practically useful products of alkenes transformation, such as dimers, oligomers, and polymers, still remains topical. Here we studied catalytic activity of differently structured zirconocenes (10 examples of cyclopentadienyl and indenyl complexes) and co-catalysts activating the system, namely HAlBui2, MMAO-12 or (Ph3C)[B(C6F5)4] at low activator/Zr ratios in 1-hexene oligomerization reaction. The influence of catalyst structure and system composition on alkene conversion, type of products formed and reaction stereoselectivity was investigated. The composition of hydride intermediates forming in the systems L2ZrCl2 (L2= ansa-Me2CCp2)-HAlBui2-activator was studied by NMR and the participation of biszirconium hydride complex as the precursor of catalytically active sites of the alkene dimerization reaction was shown.