N.M.R. study of segmental molecular interactions in liquid crystals

Abstract

A simple statistical model of interacting non-rigid molecules, based on a perturbation expansion of the pair correlation function and the additivity of segmental interactions, is applied to the study of orientational order as measured by N.M.R. in the nematic and S_A phases of 4-n-alkyl-4′-cyanobiphenyls (N-CB, N = 5 to 8), the nematic and S_C phases of 4-n-alkyloxybenzoic acids (N-OBA, N = 7, 8) and the D _h0 columnar discotic phase of hexa-alkyloxytriphenylenes (N-THE, N = 5 to 8). The order parameters of each homologous series are correctly described in terms of two isotropic and two anisotropic segmental coupling constants. The model predicts certain relations among coupling constants pertaining to different homogous series. These predictions are supported by the results obtained for the three types of compounds studied.     

Unconventional carrier-mediated ferromagnetism above room temperature in ion-implanted (Ga,Mn)P:C

Ion implantation of Mn ions into hole-doped GaP has been used to induce ferromagnetic behavior above room temperature for optimized Mn concentrations near 3 at. %. The magnetism is suppressed when the Mn dose is increased or decreased away from the 3 at. % value, or when n-type GaP substrates are used. At low temperatures the saturated moment is on the order of 1 Bohr magneton, and the spin wave stiffness inferred from the Bloch-law T(3/2) dependence of the magnetization provides an estimate T(c)=385 K of the Curie temperature that exceeds the experimental value, T(c)=270 K. The presence of ferromagnetic clusters and hysteresis to temperatures of at least 330 K is attributed to disorder and proximity to a metal-insulating transition.     

Synthesis of 2H-labeled alkoxyethyl phosphodiester (AZT) derivatives for solid-state 2H-NMR studies

Two specifically ²H-labeled alkoxyethyl phosphodiester AZT derivatives 9 and 14 were synthesized. Pilot [²H]-solid-state nmr experiments on conjugate 14 demonstrated their usefulness in studying interactions with model or biological membranes.     

Ultra-performance liquid chromatography/tandem mass spectrometry method for the determination of lercanidipine in human plasma

A simple, sensitive and rapid ultra-performance liquid chromatography/positive electrospray ionization tandem mass spectrometry (UPLC/ESI-MS/MS) method has been developed and validated for the determination of lercanidipine in human plasma. Lercanidipine and the internal standard, nicardipine, were extracted from plasma by liquid-liquid extraction using tert-butyl methyl ether as the extraction solvent. UPLC analysis was performed isocratically on an AcQuity UPLC BEH C18 analytical column (2.1 x 50.0 mm i.d., particle size 1.7 microm). The mobile phase consisted of 70% acetonitrile in water containing 0.2% v/v formic acid and pumped at a flow rate of 0.30 mL/min. ESI in positive ion mode, with multiple reaction monitoring (MRM), was chosen for the detection of the analytes. The assay was linear over a concentration range of 0.05-30 ng/mL for lercanidipine with a limit of quantitation of 0.05 ng/mL. Quality control samples (0.05, 0.15, 15 and 25 ng/mL) in five replicates from five of analytical runs demonstrated intra-assay precision (% CV < or =7.3%), inter-assay precision (% CV < or =6.1%) and an overall accuracy (% relative error) of less than 6.2%. A run time of less than 1.0 min for each sample made it possible to analyze a large number of human plasma samples per day. The method can be used to quantify lercanidipine in human plasma covering a variety of pharmacokinetic or bioequivalence studies.     

N.M.R. study of segmental molecular interactions in liquid crystals

A simple statistical model of interacting non-rigid molecules, based on a perturbation expansion of the pair correlation function and the additivity of segmental interactions, is applied to the study of orientational order as measured by N.M.R. in the nematic and S_A phases of 4-n-alkyl-4'-cyanobiphenyls (N-CB, N = 5 to 8), the nematic and S_C phases of 4-n-alkyloxybenzoic acids (N-OBA, N = 7, 8) and the D_h0 columnar discotic phase of hexa-alkyloxytriphenylenes (N-THE, N = 5 to 8). The order parameters of each homologous series are correctly described in terms of two isotropic and two anisotropic segmental coupling constants. The model predicts certain relations among coupling constants pertaining to different homogous series. These predictions are supported by the results obtained for the three types of compounds studied.     

A Unified Mechanism for the PhCOCOOH-mediated Photochemical Reactions: Revisiting its Action and Comparison to Known Photoinitiators

Since 2014, we have introduced in literature the use of phenylglyoxylic acid (PhCOCOOH), a small and commercially available organic molecule, as a potent promoter in a variety of photochemical processes. Although PhCOCOOH has a broad scope of photochemical reactions that can promote, the understanding of its mode of action in our early contributions was moderate. Herein, we are restudying and revisiting the mechanism of action of PhCOCOOH in most of these early contributions, providing a unified mechanism of action. Furthermore, the understanding of its action as a photoinitiator opened a new comparison study with known and commercially available photoinitiators.     

Design and synthesis of fluorescent shell functionalized polymer micelles for biomedical application

pH‐sensitive polymers can be defined as polyelectrolytes that include in their structure weak acidic or basic groups that either accept or release protons in response to a change in the environmental pH. This work summarizes the design, synthesis, and potential applications of pH‐responsive fluorescent copolymers in the biomedical field. This was achieved using atom transfer radical polymerization (ATRP) of tert‐butyl acrylate using a CuBr/N,N,N′,N″N″‐pentamethyldiethylenetriamine catalyst system in conjunction with an alkyl bromide as the initiator. Well‐defined macroinitiators based on poly(tert‐butyl acrylate) with narrow molecular weight distributions were obtained by the addition of an appropriate solvent system in order to create a homogeneous catalytic system. The addition of n‐butyl acrylate as a second building block in order to create well‐defined poly(tert‐butyl acrylate)‐b‐poly(n‐butyl acrylate) block copolymers (PtBA‐b‐PnBA) followed by chemical modification of the block copolymers and functionalization with an appropriate fluorescent compound are the basis for the preparation of well‐defined fluorescent pH‐sensitive micelles. Thus, prepared water soluble nanosized pH‐sensitive micelles consisting of hydrophobic poly(n‐butyl acrylate) core and hydrophilic polyacrylic acid shell decorated with an appropriate fluorescent compound determined their potential applications of these systems in the field of biomedicine as biosensors, controlled drug delivery systems, and so on. In this respect, the cell viability and internalization of the polymer micelles were studied.     

Thin porous anodic alumina films: Interface trap density determination

The electrical properties of thin porous alumina films in the form of MOS structures were studied with dielectric spectroscopy at room temperature. The thickness of the samples was found to be approximately 95 nm with a cross section area of 1.6×10⁻³ cm².C-V andG-V measurements were performed by applying a loop sweep voltage 2.0 V to −5.0 V. Correction to the measurements were performed by considering a series resistanceR _S and leakage currentI _DC. TheC-V results show hysteresis effects due to the presence of positive charges in porous alumina. These charges may be are attributed to the residual electrolyte during the anodization process in the sample preparation. Three distinct regions in theC-V results are observed, namely the inversion, the depletion and the accumulation regions. In the voltage region, where depletion of carriers is observed,C-f andG-f measurements were recorded in the frequency range 1 Hz to 10⁶ Hz. The conductance method was applied for the calculation of the density D_it of carriers, trapped in the interface between insulator and semiconductor, and of the response time τ_it as a function of the applied bias voltage were performed. The values obtained for D_it and τ_it are of the order of 3×10¹² eV⁻¹ cm⁻² and 10⁻³ s, respectively, and they are voltage dependent. Paper presented at the Patras Conference on Solid State Ionics — Transport Properties, Patras, Greece, Sept. 14 – 18, 2004.     

Artificial Neural Networks for Noise Removal in Data-Sparse Charged Particle Imaging Experiments

We present the first demonstration of artificial neural networks (ANNs) for the removal of Poissonian noise in charged particle imaging measurements with very low overall counts. The approach is successfully applied to both simulated and real experimental image data relating to the detection of photoions/photoelectrons in unimolecular photochemical dynamics studies. Specific examples consider the multiphoton ionization of pyrrole and (S)-camphor. Our results reveal an extremely high level of performance, with the ANNs transforming images that are unusable for any form of quantitative analysis into statistically reliable data with an impressive similarity to benchmark references. Given the widespread use of charged particle imaging methods within the chemical dynamics community, we anticipate that the use of ANNs has significant potential impact – particularly, for example, when working in the limit of very low absorption/photoionization cross-sections, or when attempting to reliably extract subtle image features originating from phenomena such as photofragment vector correlations or photoelectron circular dichroism.     

High-temperature ferromagnetism in Zn1−xMnxO semiconductor thin films

Clear evidence of ferromagnetic behavior at temperatures >400 K as well as spin polarization of the charge carriers have been observed in Zn_1−xMn_xO thin films grown on Al₂O₃ and MgO substrates. The magnetic properties depended on the exact Mn concentration and the growth parameters. In well-characterized single-phase films, the magnetic moment is 4.8 μ_B/Mn at 350 K, the highest moment yet reported for any Mn doped magnetic semiconductor. Anomalous Hall effect shows that the charge carriers (electrons) are spin-polarized and participate in the observed ferromagnetic behavior.