Extending the source-sink potential method to include electron-nucleus coupling.

The source-sink potential (SSP) method provides a simple tool for the qualitative analysis of the conductance of molecular electronic devices, and often analytical expressions for the conductance can be obtained. Here, we extend the SSP approach to account for decoherent, inelastic electron transport by including the non-adiabatic coupling between the electrons and the nuclei in the molecule. This coupling results in contributions to electron transport that can modify the qualitative structure-conductance relationships that we unraveled previously with SSP. In the approach proposed, electron-nucleus interactions are treated starting from the harmonic approximation for the nuclei, using a non-perturbative approach to account for the non-adiabatic coupling. Our method qualitatively describes experimentally observed phenomena and allows for a simple analysis that often provides analytical formulas in terms of the physical parameters of the junction, e.g., vibrational energies, non-adiabatic coupling, and molecule-contact coupling.

Non-Hermitian quantum mechanics and exceptional points in molecular electronics.

In non-Hermitian (NH) quantum mechanics, Hamiltonians are studied whose eigenvalues are not necessarily real since the condition of hermiticity is not imposed. Certain symmetries of NH operators can ensure that some or all of the eigenvalues are real and thus suitable for the description of physical systems whose energies are always real. While the mathematics of NH quantum mechanics is well developed, applications of the theory to real quantum systems are scarce, and no closed system is known whose Hamiltonian is NH. Here, we consider the elementary textbook example of a NH Hamiltonian matrix, and we show how it naturally emerges as a simplifying concept in the modeling of molecular electronic devices. We analyze the consequences of non-Hermiticity and exceptional points in the spectrum of NH operators for the molecular conductance and the spectral density of simple models for molecules on surfaces.

Waveguide-coupled drop filters on SOI using quarter-wave shifted sidewalled grating resonators.

We report on the design, fabrication, and demonstration of waveguide coupled channel drop filters at 1550 nm, on a silicon-on-insulator (SOI) substrate. These devices rely on resonant power transfer from a bus waveguide to side-walled Bragg resonators with quarter-wave shifts in the middle. By employing a second mirror resonator, and a tap-off waveguide, reflections along the bus waveguide can be reduced, leading to realization of circulator-free resonance filters. These devices were fabricated on SOI using e-beam lithography and inductively coupled plasma (ICP) etching. Fabricated devices with two coupled cavities are demonstrated to have rejection ratios greater than 20 dB and 3-dB bandwidths of 110 GHz, close to the values predicted by numerical modeling. We also demonstrate power tap-off at resonance of around 16 dB.

Effect of thermal annealing on the kinetics of rehydroxylation of Eu3+:La2O3 nanocrystals.

Europium-doped lanthanum oxide (5 mol % Eu(3+):La(2)O(3)) was prepared by calcining europium-doped lanthanum hydroxide (5 mol % Eu(3+):La(OH)(3)) previously synthesized by a simple hydrothermal method. Interestingly, we observed different emission Eu(3+) signatures depending on the phase of the host (lanthanum oxide or hydroxide) by cathodoluminescence. Taking into account that lanthanum oxide easily rehydroxylates in air, for the first time, we report the use of cathodoluminiscence as a novel characterization technique to follow the lanthanum oxide rehydroxylation reaction versus time according to different annealing procedures. Additionally, differential thermal-thermogravimetric analysis, infrared spectroscopy, and X-ray diffraction techniques were used to identify the phases formed from the Eu(3+):La(OH)(3) depending on temperature and to study the evolution of La(2)O(3) to La(OH)(3) versus time. The results showed that the higher the temperature and the longer the annealing time, the higher the resistance to rehydroxylation of the Eu(3+):La(2)O(3) sample.

Structure-based design, synthesis and A-site rRNA co-crystal complexes of novel amphiphilic aminoglycoside antibiotics with new binding modes: a synergistic hydrophobic effect against resistant bacteria.

Incorporation of an hydrophobic (phenethylamino)ethyl ether at C2″ of N1-(HABA)-3',4'-dideoxyparomomycin led to a novel analog with an excellent antibacterial profile against a host of resistant bacteria.

Toward Overcoming Staphylococcus aureus Aminoglycoside Resistance Mechanisms with a Functionally Designed Neomycin Analogue.

Deoxygenation of the diol groups in rings A and D of neomycin in combination with the introduction of an N1-(l)-HABA group in the 2-deoxystreptamine subunit (ring B) leads to a novel and potent antibiotic (1) with activity against strains of S. aureus carrying known aminoglycoside resistance determinants, as well as against an extended panel of Methicillin-resistant S. aureus isolates (n = 50). Antibiotic 1 displayed >64 fold improvement in MIC50 and MIC90 against this MRSA collection when compared to the clinically relevant aminoglycosides amikacin and gentamicin. The synthesis was achieved in six steps and 15% overall yield.