New infrared emitting d-f (ruthenium(II)-neodymium(III)) heterobimetallic complexes with alkoxy(silyl) functional groups have been prepared. Visible excitation evidenced energy transfer processes from the ruthenium(II) donor to neodymium(III) acceptors leading to infrared emission. Energy transfer rates (kEnT) and efficiency of energy transfer (ηEnT) are, respectively, 0.61 × 107s-1 and 44% for RuL1-NdL3 complex. Larger values of kEnT (3.04 × 107 s-1) and ηEnT (84%) were detected for RuL2-NdL4 complex. RuL1-NdL3 and RuL2-NdL4 complexes were fully characterized by elementary analysis (EA), mass spectrometry (MS), Fourier transform infrared spectroscopy (FTIR) and Fourier transform Raman spectroscopy (FT-Raman). Total correlation spectroscopy (TOCSY1D), 1H{13C} heteronuclear single quantum correlation (HSQC) and 1H{13C} heteronuclear multiple bond correlation (HMBC) nuclear magnetic resonance (NMR) analyses were also carried out to characterize NdL3 and RuL1-NdL3 complexes. The presence of trialkoxysilyl-substituted ligands would allow further grafting onto any silica or silicated surface aiming at applications as new luminescent near infrared (NIR)-emitting biosensors or biomarkers.

This paper reports the synthesis and characterization of Cr3+-doped alumina by the sol-gel non-hydrolytic methodology. The resulting sample was treated at different temperatures. X-ray diffraction revealed that the ruby phase emerged in the sample treated at 1100 ºC, which was later confirmed by absorption bands correspondent to Cr3+ ions allowed transitions at 4A2 → 4T1, 4T2, and forbidden at 4A2 → 2T1, 2E, observed by diffuse reflectance UV-Vis. The luminescence spectroscopy showed the intensity band at 694 nm in red region, characterized of the Cr3+ ion. The peaks at 702 and 705 nm correspond to N1 and N2 lines, respectively, which arose from the second and fourth nearest-neighbor exchange-coupled pairs of chromium(III) ion, respectively, ascribed to high chromium(III) concentration. The Cr3+ cluster formation was observed in electron paramagnetic resonance signal as discussed in this work. Nuclear magnetic resonance evidenced that the 27 Al symmetry changed in the samples treated between 900 and 1100 ºC.

New luminescent organic-inorganic hybrid particles based on Tb-doped aluminates and asparagine (Asn) surface modifiers were investigated. The Tb3+ doped inorganic core was obtained by spray pyrolysis, at 200 ºC γ-AlOOH (BOE:Tbx%) or at 700 ºC γ-Al2O3 (γTA:Tbx%). The reaction of Asn with boehmite in water disaggregated the sub-micronic boehmite particles to give stable dispersion of surface modified nanoparticles Asn:BOE:Tbx% (x = 1 or 5). Concerning the Asn:γTA:Tbx% system, an Asn film wrapping alumina particles was observed. Photoluminescence spectra exhibited the bands assigned to Tb3+5D4 → 7FJ = 6-3 transitions. A broad absorption band (240 nm) was assigned to the host (aluminate) to ion (Tb3+) energy transfer. Efficient energy transfer was observed when active ions are incorporated in the defect-spinel structure of γTA, whereas it was relatively weak for BOE:Tb where Tb3+ are bonded to the hydroxyls groups at nanocrystals surface. It is noticeable that Asn strengthens the linkage of Tb3+ with the aluminate matrix, enhancing the host to dopant energy transfer.

Silver containing heavy metal oxide glasses and glass ceramics of the system WO3-SbPO4-PbO-AgCl with different AgCl contents have been prepared and their thermal, structural and optical properties characterized. Glass ceramics containing metallic silver nanoparticles have been prepared by annealing glass samples at temperatures above the glass transition and analyzed by transmission electron microscopy and energy dispersive X-ray microanalysis. The presence of the metallic clusters has been also confirmed by the observation of a surface plasmon resonance band in the visible range. Cyclic voltammetric measurements indicated the presence of metallic silver into the glasses, even before to perform the thermal treatment.