On the composition of gastroliths from broiler breeders.

The purpose of this study was to ascertain the composition and origin of certain gastroliths or gizzard stones from broiler breeders (Gallus gallus domesticus). Fourier transform infrared spectroscopy (FTIR) and X-ray powder diffraction techniques were used as analysis tools. The main components resulted to be organic fibre and minerals referred to a pegmatite rock (quartz, feldspar albite and haematite) used as grit. Although the generally accepted purpose of gastroliths in chicken is the crushing and grinding of foodstuff in the ventriculus, the importance of mineral uptake from grit of iron and other essential elements such as Al, Ca, K, Cl, P, Ti, Mn, Mg, Cu, Zn and Zr (in ppm) as a secondary effect of the abrasion and dissolution of gastroliths should not be disregarded.

Slow magnetic relaxation mechanisms in erbium SIMs.

The magnetic properties of two similar Er(3+) complexes have been investigated. [Er(tpm)3(bipy)] (Htpm = 1,1,1-trifluoro-5,5-dimethyl-2,4-hexanedione and bipy = 2,2'-bipyridine) displays thermally activated slow relaxation of magnetisation under a zero direct-current (DC) field. Under an applied HDC field of 1000 G, [Er(tpm)3(bipy)] exhibits two thermally activated processes with energy barriers of 9 and 40 K, while [Er(tfa)3(bipy)] (Htfa = 4,4,4-trifluoro-1-(2-furyl)-1,3-butanedione) shows only one activated process with a barrier of 15 K. Both compounds are luminescent in the solid state, emitting in the near IR region.

Active layer solution-processed NIR-OLEDs based on ternary erbium(III) complexes with 1,1,1-trifluoro-2,4-pentanedione and different N,N-donors.

Using a fluorinated 1,1,1-trifluoro-2,4-pentanedione (Htfac) ligand and either 2,2'-bipyridine (bipy), bathophenanthroline (bath) or 5-nitro-1,10-phenanthroline (5NO2phen) as an ancillary ligand, three new ternary erbium(iii) octacoordinated complexes have been synthesized. The single crystal structures of the new complexes (namely [Er(tfac)3(bipy)], [Er(tfac)3(bath)] and [Er(tfac)3(5NO2phen)]) have been determined and their properties have been investigated by Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy and thermodynamic analysis. After ligand-mediated excitation of these complexes in the UV, they all show the characteristic near-infrared (NIR) luminescence of the corresponding Er(3+) ion at 1532 nm. The same emission in the C-band transmission window can also be obtained from the solution-processed organic light-emitting diodes (OLEDs) with structure: glass/ITO/PEDOT:PSS/[Er(tfac)3(N,N-donor)]/Ca/Al. In spite of the fact that the photoluminescence intensity of [Er(tfac)3(5NO2phen)] is stronger than those of [Er(tfac)3(bipy)] and [Er(tfac)3(bath)], the best electroluminescence results correspond to the OLED based on the [Er(tfac)3(bath)] complex, as a consequence of the superior electron transport capabilities of bathophenanthroline.

Effect of the capping ligand on luminescent erbium(III) ß-diketonate single-ion magnets.

Erbium complexes featuring ß-diketonate ligand 2,4-hexanedione (Hh) and N,N-donor-ligands 2,2'-bipyridine (bipy), 5-nitro-1,10-phenanthroline (5NO2phen) and bathophenanthroline (bath) have been synthesized. The structures of the ternary complexes [Er(h)3(bipy)], [Er(h)3(5NO2phen)] and [Er(h)3(bath)] have been determined by single crystal X-ray diffraction. Excitation of the complexes in the ultraviolet region (337 nm) led to near infrared (NIR) luminescence at 1532 nm characteristic of the trivalent erbium ion in the three compounds, with an improved antenna effect in the 5-nitro-1,10-phenanthroline complex. The AC susceptibility studies conducted at frequencies ranging from 33 to 9995 Hz and at temperatures in the 1.7 to 10 K range revealed that the application of a static magnetic field induces a slow magnetic relaxation in all three compounds. The complex with the bulkier capping ligand (bathophenanthroline) exhibits the highest energy barrier U/k(B) = 23 K.