C60/NiFe combination as a promising platform for molecular spintronics

Spintronics based on ferromagnetic metals and organic semiconductors has attracted great interest in recent years. Molecular-based spintronic devices, such as magnetic tunnel junctions, have been demonstrated with performances competing with those of conventional inorganic devices. Still, there is huge margin for improvement, as many details about the injection of spin-polarized electrons into the molecular layer remain not completely understood. In order to achieve better understanding and control of the physical mechanisms, it is necessary to explore various combinations of ferromagnetic metals and organic semiconductors. In this letter, we study the properties of the combination between the ferromagnetic metal NiFe (commonly known as Permalloy or Py) and the molecular system C60. We produced C60/Py bilayers and characterized them structurally, electrically and magnetically. The C 60 films grow smoothly on both Py and SiO2 substrates, and we estimate that a 5-nm-thick C60 film covers completely the surface underneath without leaving pinholes and can be therefore used in a vertical device, as confirmed by electrical characterization. Furthermore, the C 60 film is robust against the deposition of the top metal electrode, being the intermixing layer of only 1-2 nm at the C60/Py interface. Finally, we show that the magnetic properties of Py are not affected by the deposition sequence, and that a 5-nm-thick Py layer on top of a C60 layer keeps its magnetic properties intact. These results show that the combination between Py and C60 provides a robust template platform for the development of molecular spintronics, and can be used later on for more sophisticated investigations, such as the role of the interfaces in the spin injection.Fil: Gobbi, M.. No especifíca;Fil: Pascual, A.. No especifíca;Fil: Golmar, Federico. Instituto Nacional de Tecnología Industrial; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Llopis, R.. No especifíca;Fil: Vavassori, P.. No especifíca;Fil: Casanova, F.. No especifíca;Fil: Hueso, L. E.. No especifíca

Laser ablation is superior to TACE in large-sized hepatocellular carcinoma: A pilot case-control study

Background:Limited therapies are available for large ( 6540 mm) unresectable hepatocellular carcinoma (HCC). Currently, the standard treatment with transarterial chemoembolisation (TACE) is unsatisfactory with high recurrence rate and limited effect on survival. Laser Ablation (LA) has emerged as a relatively new technique characterized by high efficacy and good safety. This study is aimed to evaluate the efficacy of LA in comparison to TACE in patients with large HCC. Methods: Eighty-two patients with a single HCC nodule 6540 mm (BCLC stage A or B) were enrolled in this case-control study. Forty-one patients were treated with LA and 41 patients were treated with TACE. Response to therapy was evaluated according to the mRECIST criteria. Survival was calculated with Kaplan-Meier from the time of cancer diagnosis to death with values censored at the date of the last follow-up. Results: Twenty-six (63.4%) and 8 (19.5%) patients had a complete response after LA and TACE, respectively (p < 0.001). Subsequently we stratified the HCCs in 3 categories according to the nodule size: 40-50 mm, 51-60 mm, and > 60 mm. LA resulted superior to TACE especially in nodules ranging between 51 and 60 mm in diameter, with a complete response rate post-LA and post-TACE of 75% and 14.3%, respectively (p = 0.0133). The 36 months cumulative survival rate in patients treated with LA and TACE was 55.4% and 48.8%, respectively. The disease recurrence rates after LA and TACE were 19.5% and 75.0%, respectively. Conclusions: LA is a more effective therapeutic option than TACE in patients with solitary large HCC

Vortex state suppression in an hexagonal array of interacting Py triangular rings

The magnetization reorientation process (MRP) of magnetic nanostructures displays novel features thanks to confinements effects due to nanostructures reduced dimensionality. As the applied field varies, the nanostructures magnetic configuration changes via domain walls (DWs) nucleation or annihilation; if magnetic materials with negligible magnetocrystalline anisotropy are used, this process is usually ruled just by the nanostructures shape. To make the MRP more reproducible and less sensitive to shape defects and to possible high energy magnetic configurations, e.g. vortex cores, the ring geometry is preferred. In this case, the magnetization process develops through magnetic configurations that are quite independent of the specific ring geometry [1,2], the so called onion state (OS) and the vortex state (VS). When inter-ring distance is small (less than one half of ring size) the dipolar interaction influence on the MRP becomes significant. In particular, during the MRP of triangular rings the DWs move and are trapped by ring corners so that the stray magnetic field may be intense. The influence of inter-ring interactions changes due to the rings shape, relative position and magnetic configuration [2]. The fields that produce the switch between OS and VS may accordingly change and a ring magnetic configuration may get less stable or even suppressed. In this contribution, we present the results obtained on an hexagonal array (HA) of Py equilateral triangular rings. The rings thickness is 25 nm, their side is 1.8 μm and their width is 230 nm. We adopt the hexagonal pattern and a reduced corner to corner distance (50 nm) in order to maximize the effect of inter-ring magnetic interactions. The magnetic reversal process was monitored for different directions of the in-plane applied field (H) through MFM measurements and longitudinal and diffraction magneto-optical Kerr effect, LMOKE and DMOKE, respectively. LMOKE gives access to the H dependence of the in-plane magnetization components; DMOKE to the H dependence of the magnetic form factor, also related to the symmetry of the nanostructure magnetic configuration [2]. Due to the presence of strong dipolar interactions, the rings of the HA display a long range magnetic order and, for a given H, they all display the same configuration. The MRP proceeds through the development of a VS in between two specularly symmetric OS; the VS is featured by a well-defined step in the LMOKE loops and by a peak in the DMOKE loops. For H parallel to the rings side (H//), the H range where the VS is stable is narrower than that observed in the isolated rings case [2]. For H perpendicular to the rings side (H_perp), the VS disappears whereas in the isolated case the VS was clearly observed. If the angle between H and a ring side, θ, is varied from 0, i.e. H//, to 30, i.e. H_perp, the width of the VS range of stability smoothly decreases and then goes abruptly to 0 for θ ~ 30. If θ is slightly varied around 30, the VS is not observed, as well. The observed difference between the H// and H_perp geometries may be due to the interplay between shape anisotropy energy and dipolar interaction energy; in H// shape anisotropy stabilizes the VS whilst in H_perp, as this direction is a symmetry axis of the triangular ring, shape anisotropy is less effective and the dipolar term prevails, stabilizing the OS configurations and canceling the VS. Indeed, the OS is the configuration where dipolar interaction are stronger, as 2 out of the 3 ring corners display a DW. The data will be discussed together with the results of micromagnetic calculations performed with the OOMMF software. The HA was simulated using groups of N rings (N = 3, 7) having different relative positions, to access different flux-closure configurations. The results will be discussed in terms of the stability of the vortex state. This work was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under Grant Agreement n°228673 (MAGNONICS). [1] M.F. Lai et al., J. Magn. Magn. Mater., 322 (2010) 92 [2] P. Vavassori, D. Bisero et al., Phys. Rev. B 78 (2008) 174403

Synthesis, Characterization, Fluorescence Properties, and DFT Modeling of Difluoroboron Biindolediketonates

We report a simple and efficient strategy to enhance the fluorescence of biocompatible biindole diketonates (bdks) in the visible spectrum through difluoroboronation (BF2bdks complexes). Emission spectroscopy testifies an increase in the fluorescence quantum yields from a few percent to as much as >0.7. This massive increment is essentially independent of substitutions at the indole (-H, -Cl, and -OCH3) and corresponds to a significant stabilization of the excited state with respect to non-radiative decay mechanisms: the non-radiative decay rates are reduced by as much as an order of magnitude, from 109 s−1 to 108 s−1, upon difluoroboronation. The stabilization of the excited state is large enough to enable sizeable 1O2 photosensitized production. Different time-dependent (TD) density functional theory (DFT) methods were assessed in their ability to model the electronic properties of the compounds, with TD-B3LYP-D3 providing the most accurate excitation energies. The calculations associate the first active optical transition in both the bdks and BF2bdks electronic spectra to the S0 → S1 transition, corresponding to a shift in the electronic density from the indoles to the oxygens or the O-BF2-O unit, respectively

Synthesis, Characterization and DNA-Binding Affinity of a New Zinc(II) Bis(5-methoxy-indol-3-yl)propane-1,3-dione Complex

The novel zinc(II) µ-oxo-bridged-dimeric complex [Zn2(µ-O)2(BMIP)2] (BMIP = 1,3-bis(5-methoxy-1-methyl-1H-indol-3-yl)propane-1,3-dione), 1, was synthetized and fully characterized. The spectral data indicate a zincoxane molecular structure, with the BMIP ligand coordinating in its neutral form via its oxygen atoms. Structural changes in 1 in dimethylsulfoxide (DMSO) were evidenced by means of spectroscopic techniques including infrared absorption and nuclear magnetic resonance, showing DMSO entrance in the coordination sphere of the metal ion. The resulting complex [Zn2(µ-O)2(BMIP)2(DMSO)], 2, readily reacts in the presence of N-methyl-imidazole (NMI), a liquid-phase nucleoside mimic, to form [Zn2(µ-O)2(BMIP)2(NMI)], 3, through DMSO displacement. The three complexes show high thermal stability, demonstrating that 1 has high affinity for hard nucleophiles. Finally, with the aim of probing the suitability of this system as model scaffold for new potential anticancer metallodrugs, the interactions of 1 with calf thymus DNA were investigated in vitro in pseudo-physiological environment through UV-Vis absorption and fluorescence emission spectroscopy, as well as time-resolved fluorescence studies. The latter analyses revealed that [Zn2(µ-O)2(BMIP)2(DMSO)] binds to DNA with high affinity upon DMSO displacement, opening new perspectives for the development of optimized drug substances

Development of a computer-assisted instrumentation curriculum for physics students: Using LabVIEW and Arduino platform

[[abstract]]We propose an integrated curriculum to establish essential abilities of computer programming for the freshmen of a physics department. The implementation of the graphical-based interfaces from Scratch to LabVIEW then to LabVIEW for Arduino in the curriculum ‘Computer-Assisted Instrumentation in the Design of Physics Laboratories’ brings rigorous algorithm and syntax protocols together with imagination, communication, scientific applications and experimental innovation. The effectiveness of the curriculum was evaluated via statistical analysis of questionnaires, interview responses, the increase in student numbers majoring in physics, and performance in a competition. The results provide quantitative support that the curriculum remove huge barriers to programming which occur in text-based environments, helped students gain knowledge of programming and instrumentation, and increased the students’ confidence and motivation to learn physics and computer languages.[[notice]]補正完

Synthesis of a new sulfonated-hexachlorobiphenyl standard for environmental analysis, ecotoxicological, and toxicological studies

Sulfonated-polychlorinated biphenyls (sulfonated-PCBs) are a newly discovered class of PCB metabolites. They were observed for the first time in polar bear serum and lately, in soil, together with hydroxy-sulfonated-PCBs. Their presence is ubiquitous in soils, and their estimated physical chemical properties show high mobility in water, compared to the parent compounds. However, no single pure standards exist so far and therefore their quantification in the environmental matrices is not accurate. Additionally, pure standards are needed to experimentally determine their physical chemical properties, as well as the ecotoxicological and toxicological characteristics. In the present work, the challenging goal of preparing a polychlorinated biphenyl monosulfonic acid was achieved exploring different synthetic approaches, along which the selection of the starting material resulted in a crucial point. Using PCB-153 (2,2'-4,4'-5,5'-hexachloro-1,1'-biphenyl) the synthesis afforded, as the major species, a side compound. On the contrary, the use of PCB-155 (2,2'-4,4'-6,6'-hexachloro-1,1'-biphenyl), a symmetric hexachlorobiphenyl derivative showing chlorine atoms at all the ortho positions, gave the target sulfonated-PCB compound. In this case, sulfonation was successfully carried out through a two-step procedure, involving chlorosulfonylation and the subsequent hydrolysis of the chlorosulfonyl intermediate

Cyberknife Radiosurgery for Prostate Cancer after Abdominoperineal Resection (CYRANO): The Combined Computer Tomography and Electromagnetic Navigation Guided Transperineal Fiducial Markers Implantation Technique

In this technical development report, we present the strategic placement of fiducial markers within the prostate under the guidance of computed tomography (CT) and electromagnetic navigation (EMN) for the delivery of ultra-hypofractionated cyberknife (CK) therapy in a patient with localized prostate cancer (PCa) who had previously undergone chemo-radiotherapy for rectal cancer and subsequent abdominoperineal resection due to local recurrence. The patient was positioned in a prone position with a pillow under the pelvis to facilitate access, and an electromagnetic fiducial marker was placed on the patient’s skin to establish a stable position. CT scans were performed to plan the procedure, mark virtual points, and simulate the needle trajectory using the navigation system. Local anesthesia was administered, and a 21G needle was used to place the fiducial markers according to the navigation system information. A confirmatory CT scan was obtained to ensure proper positioning. The implantation procedure was safe, without any acute side effects such as pain, hematuria, dysuria, or hematospermia. Our report highlights the ability to use EMN systems to virtually navigate within a pre-acquired imaging dataset in the interventional room, allowing for non-conventional approaches and potentially revolutionizing fiducial marker positioning, offering new perspectives for PCa treatment in selected cases