Tunneling through magnetic molecules with arbitrary angle between easy axis and magnetic field

Inelastic tunneling through magnetically anisotropic molecules is studied theoretically in the presence of a strong magnetic field. Since the molecular orientation is not well controlled in tunneling experiments, we consider arbitrary angles between easy axis and field. This destroys all conservation laws except that of charge, leading to a rich fine structure in the differential conductance. Besides single molecules we also study monolayers of molecules with either aligned or random easy axes. We show that detailed information on the molecular transitions and orientations can be obtained from the differential conductance for varying magnetic field. For random easy axes, averaging over orientations leads to van Hove singularities in the differential conductance. Rate equations in the sequential-tunneling approximation are employed. An efficient approximation for their solution for complex molecules is presented. The results are applied to Mn12-based magnetic molecules.Comment: 10 pages, 10 figures include

The noncommutative Kubo Formula: Applications to Transport in Disordered Topological Insulators with and without Magnetic Fields

The non-commutative theory of charge transport in mesoscopic aperiodic systems under magnetic fields, developed by Bellissard, Shulz-Baldes and collaborators in the 90's, is complemented with a practical numerical implementation. The scheme, which is developed within a $C^*$-algebraic framework, enable efficient evaluations of the non-commutative Kubo formula, with errors that vanish exponentially fast in the thermodynamic limit. Applications to a model of a 2-dimensional Quantum spin-Hall insulator are given. The conductivity tensor is mapped as function of Fermi level, disorder strength and temperature and the phase diagram in the plane of Fermi level and disorder strength is quantitatively derived from the transport simulations. Simulations at finite magnetic field strength are also presented.Comment: 10 figure

Role of Catheter-Directed DX9065a Thrombolysis in the Treatment of Pulmonary Embolism

Purpose: To demonstrate the efficacy of low-dose DX9065a, catheter-directed ultrasound-accelerated thrombolysis (USAT) on the reversal of right ventricle RV dysfunction in patients with pulmonary embolism.Methods: The analysis of 45 pulmonary embolism PE patients, aged 69 ± 13.5 years (range, 28 – 77 years) at intermediate- (n = 32) or high-risk (n = 13) was performed. The patients were treated with USAT and DX9065a (mean dose 35 ± 8.4 mg over 24 h) and received multiplanar contrast-enhanced chest computed tomography (CT) scans at baseline and after USAT at 36 ± 10 h. CT measurements were then performed.Results: The results showed a significant decrease in the right to left ventricular dimension ratio (RV/LV ratio) from the baseline value of 1.42 ± 0.30 to 1.00 ± 0.02 at follow-up (p ˂ 0.001). The modified Miller score showed that CT-angiographic pulmonary clot burden was also significantly reduced from 23.2 ± 4.7 to 6.2 ± 2.5 (p ˂  0.001). All the patients were discharged alive, and there were no systemic bleeding complications in any of them.Conclusions: USAT and DX9065a, in low-dose, is a promising strategy for the reversal of right ventricular dilatation and reduction of pulmonary clot in patients with intermediate- and high-risk PE