Fabio Piccinelli

Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes

Remarkable generality in scope of DATs/Cu catalysts for enantioselective nitroaldol reaction is described; excellent levels of stereoinduction are recorded for a range of aldehydes (ee 81-99%, 17 examples) and the possibility to employ the present catalytic system as the key step for the preparation of highly functionalized tetrahydro-isoquinolines is demonstrated.

1.3 μm emitting SrF2:Nd3+ nanoparticles for high contrast in vivo imaging in the second biological window

Novel approaches for high contrast, deep tissue, in vivo fluorescence biomedical imaging are based on infrared-emitting nanoparticles working in the so-called second biological window (1,000–1,400 nm). This allows for the acquisition of high resolution, deep tissue images due to the partial transparency of tissues in this particular spectral range. In addition, the optical excitation with low energy (infrared) photons also leads to a drastic reduction in the contribution of autofluorescence to the in vivo image. Nevertheless, as is demonstrated here, working solely in this biological window does not ensure a complete removal of autofluorescence as the specimen’s diet shows a remarkable infrared fluorescence that extends up to 1,100 nm. In this work, we show how the 1,340 nm emission band of Nd3+ ions embedded in SrF2 nanoparticles can be used to produce autofluorescence free, high contrast in vivo fluorescence images. It is also demonstrated that the complete removal of the food-related infrared autofluorescence is imperative for the development of reliable biodistribution studies.

Lanthanide doped upconverting colloidal CaF2 nanoparticles prepared by a single-step hydrothermal method: toward efficient materials with near infrared-to-near infrared upconversion emission

Colloidal Er(3+)/Yb(3+), Tm(3+)/Yb(3+) and Ho(3+)/Yb(3+) doped CaF(2) nanoparticles have been prepared by a one-pot hydrothermal procedure and their upconversion properties have been investigated.

Electrochemiluminescent functionalizable cyclometalated thiophene-based iridium(III) complexes.

A family of new functional bis-cyclometalated thiophene-based cationic iridium complexes have been prepared and fully characterized. The introduction of formyl groups into the thienyl-based cyclometalating ligand (thpy-CHO) allows one to perform further functionalizability and to confer to the whole species potentially interesting perspectives as functional materials. The X-ray crystal structures of three complexes, namely, [Ir(thpy)(2)bpy]PF(6), [Ir(thpy-CHO)(2)bpy]PF(6), and [Ir(thpy-CHO)(2)phen]PF(6), are reported. A rich reduction voltammetric pattern of the complexes is outlined, and the effect of the substituents on the cyclic voltammetric behavior is fully elucidated. Finally, the electrochemiluminescence spectra of all of the species have been obtained in acetonitrile by annihilation of the one-electron-oxidized and -reduced forms, showing very similar features with respect to the luminescence (as both the shape and energy of the emission bands).

PEG-capped, lanthanide doped GdF3 nanoparticles: luminescent and T2 contrast agents for optical and MRI multimodal imaging

A facile method for the synthesis of water dispersible Er(3+)/Yb(3+) and Tm(3+)/Yb(3+) doped upconverting GdF(3) nanoparticles is reported. Strong upconversion emissions are observed in the red (for Er/Yb doped) and near-infrared (for Tm/Yb doped) regions upon laser excitation at 980 nm. The PEG coating ensures a good dispersion of the system in water and reduces the radiationless de-excitation of the excited states of the Er(3+) and Tm(3+) ions by water molecules. The r(2) relaxivity values are quite high with respect to the common T(2)-relaxing agents (22.6 ± 3.4 mM(-1) s(-1) and 15.8 ± 3.4 mM(-1) s(-1) for the Tm/Yb and Er/Yb doped samples, respectively), suggesting that the present NPs can be interesting as T(2) weighted contrast agents for proton MRI purpose. Preliminary experiments conducted in vitro, in stem cell cultures, and in vivo, after subcutaneous injection of the lanthanide-doped GdF(3) NPs, indicate scarce toxic effects. After an intravenous injection in mice, the GdF(3) NPs localize mainly in the liver. The present results indicate that the present Er(3+)/Yb(3+) and Tm(3+)/Yb(3+) doped GdF(3) NPs are suitable candidates to be efficiently used as bimodal probes for both in vitro and in vivo optical and magnetic resonance imaging.

Nanocrystalline lanthanide-doped Lu3Ga5O12 garnets: interesting materials for light-emitting devices

Nanocrystalline Lu(3)Ga(5)O(12), with average particle sizes of 40 nm, doped with a wide variety of luminescent trivalent lanthanide ions have been prepared using a sol-gel technique. The structural and morphological properties of the powders have been investigated by x-ray powder diffraction, high resolution transmission electron microscopy and Raman spectroscopy. Structural data have been refined and are presented for Pr(3+), Eu(3+), Gd(3+), Ho(3+), Er(3+) and Tm(3+) dopants, while room temperature excited luminescence spectra and emission decay curves of Eu(3+)-, Tm(3+)- and Ho(3+)-doped Lu(3)Ga(5)O(12) nanocrystals have been measured and are discussed. The Eu(3+) emission spectrum shows typical bands due to 5D(0)-->7F(J) (J = 0, 1, 2, 3, 4) transitions and the broadening of these emission bands with the non-exponential behaviour of the decay curves indicates the presence of structural disorder around the lanthanide ions. Lanthanide-doped nanocrystalline Lu(3)Ga(5)O(12) materials show better luminescence intensities compared to Y(2)O(3), Gd(3)Ga(5)O(12) and Y(3)Al(5)O(12) nanocrystalline hosts. Moreover, the upconversion emission intensity in the blue-green region for the Tm(3+)- and Ho(3+)-doped samples shows a significant increase upon 647.5 nm excitation with respect to other common oxide hosts doped with the same lanthanide ions.

Visible luminescence of lanthanide ions in Ca3Sc2Si3O12 and Ca3Y2Si3O12

The crystalline materials Ca3Sc2Si3O12 and Ca3Y2Si3O12 were characterized by different crystal structures, as the former is a cubic garnet, while the latter is an orthorhombic compound. We investigated the optical spectroscopy of these materials doped with several trivalent lanthanide ions and compared the results for the two hosts. Polycrystalline samples were prepared by solid state reaction, both undoped and doped with the trivalent lanthanide ions Eu3+, Tb3+ and Sm3+. Emission, excitation and Raman spectra of these materials were measured at temperatures ranging from 300 to 10 K. The optical spectra were assigned and discussed, and the effects of the crystal structure of the host on the spectroscopic behaviour were addressed. The technological potential of these compounds in the field of optical materials and devices was discussed.

Enantioselective synthesis of 2,6-diaminopimelic acid derivatives. Part 3

Abstract Enantiomerically pure 2,6-diaminopimelic acid derivatives 9a – c and 10a – c have been synthesized starting from the glycine-derived chiral synthon (1′ S ,1″ S )- 1 . The absolute configuration of stereocenters introduced on 2 and 3 were assigned on the basis of 1 H NMR data and conformational analysis.

Multifunctional nanoprobes based on upconverting lanthanide doped CaF2: towards biocompatible materials for biomedical imaging

Water dispersible Gd3+,Yb3+,Er3+ and Gd3+,Yb3+,Tm3+ doped CaF2 nanoparticles (NPs) were prepared by one-pot hydrothermal synthesis using citrate ions as capping agents without the need for any post-synthesis reaction. UC emissions are easily observed in the visible and infrared regions upon NIR diode laser excitation at 980 nm. EPR spectroscopy confirms the substitutional nature of the rare-earth doping, while magnetometric studies reveal that the NPs have a useful magnetization. MRI experiments conducted in vivo show that after 40 min from the injection, the NPs localize in the liver and spleen. Electron microscopy images of liver tissue reveal that the NPs are located in the Kupffer cells, although a small amount is also found in the hepatocytes. An excitation with a 980 nm emission on the excised liver and epithelial tissue induces clearly visible UC emission. The local temperature upon 980 nm irradiation was monitored in situ and it was found to increase slowly with the exposure time, maintaining under 1-2 °C for less than 60 second exposure. The NPs show a low toxicity towards cultured HeLa cells and human primary dendritic cells (DCs), and did not induce pro-inflammatory cytokine secretion by cultured human DCs, indicating that the NPs do not cause relevant adverse reactions in immune cells. Therefore, the present NPs are suitable candidates to be efficiently used in surgery applications, where spatial resolution and lack of harmful effects on human health are important issues.

Multicolour second harmonic generation by strontium barium niobate nanoparticles

Infrared to visible second harmonic generation (SHG) has been demonstrated from 40 nm Sr0.6Ba0.4Nb2O6 nanoparticles in a broad spectral range of infrared fundamental wave excitation (800–1200 nm). The efficiency for SHG is compared with that obtained from powdered samples of larger crystallite sizes so that the mechanism leading to optical frequency conversion is discussed. The obtained results point out the possibility of using nonlinear nanoparticles for multifrequency optical imaging.