Contributions to the study of some heterocycles: LII—Mass spectra of some 3-phenyl-5-(R-thio)1,2,4-triazoles and some thiazolo[3,2-b]-1,2,4-triazoles

The fragmentation patterns of thiazolotriazoles are in agreement with the individual character of each heterocycle but there are also peaks arising both from their combined influence and from the nature of the substituents in positions 5 and 6.     

On the regularity of solutions to a parabolic system related to Maxwell's equations

The goal of this paper is to establish Hölder estimates for the solutions of a certain parabolic system related to Maxwell's equations arising in a quasi-stationary electromagnetic field.     

Electronic properties of furyl substituents at phosphorus and their influence on 31P NMR chemical shifts

The electronic properties of 2-furyl and 3-furyl substituents attached to phosphanes and phosphonium salts were studied by means of IR spectroscopy and experimental and computational (31)P NMR spectroscopy. The heteroaromatic systems proved to be electron withdrawing with respect to phenyl substituents. However, phosphorus atoms with attached furyl substituents are strongly shielded in NMR. The reason for this phenomenon was studied by solid state (31)P MAS NMR experiments. The chemical shift tensor was extracted, and the orientation within the molecules was determined. The tensor component sigma(33), which is effected the most by furyl systems, is oriented perpendicular to the P-C bonds of the substituents. P-furyl bonds are shorter than P-phenyl bonds. We assume therefore a lower ground-state energy of the molecules, because of the electron withdrawing properties of the 2-furyl systems. The sigma(para) component of the (31)P NMR magnetic shielding is therefore smaller, which results in an overall increase of the magnetic shielding.     

Decrease of luminol chemiluminescence upon exposure of human blood serum to 50 Hz electric fields

The chemiluminescence of luminol, after 1 and 2h in vitro exposure of human serum to 50 Hz electric fields of different intensities, decreases as compared to the controls. This indicates a field-induced decrease in the concentration of the free radicals. The report is limited to the key kinetic and field data, inviting independent kinetic analysis of the data in terms of reaction moments or reaction susceptibilities for the various normal modes indicated by the data.     

The Antioxidative Activity of Riboflavin in the Presence of Antipyrin. Spectroscopic Studies

The effect of Antipyrin upon the antioxidant activity of the riboflavin has been evidenced using chemiluminescent system luminol–hydrogen peroxide, in Tris–HCl buffer, pH 8.5. It was found that riboflavin antioxidant activity depends on the reaction time and the Antipyrin concentration. Using ESR spectroscopy the hydroxyl radical generation, in the mentioned chemiluminescent system, was evidenced. The interaction between reactants was also investigated by UV-VIS and fluorescence spectroscopy. The effect of Antipyrin concentration upon the riboflavin fluorescence has also been investigated. The fluorescence quenching by Antipyrin is not significant and subsequently the riboflavin fluorescence quenching doesn’t indicate an electron transfer process through diffusion-controlled mechanism. The results are discussed with relevance to the redox processes of riboflavin.     

Saturation transfer and chemical exchange measurements of the stereochemical drift occurring during the Wittig reaction

The Wittig reaction of butylidenetriphenylphosphorane with benzaldehyde using LiHMDS as base in THF was studied. The stereochemical drift (different ratio obtained in alkenes versus oxaphosphetane intermediates) was followed by low-temperature 1D NMR techniques. A retro-Wittig reaction is demonstrated using 13C and 31P saturation transfer experiments and homonuclear DPFGSE-ROE techniques.     

Dendrimers as Non-Viral Vectors in Gene-Directed Enzyme Prodrug Therapy

Gene-directed enzyme prodrug therapy (GDEPT) has been intensively studied as a promising new strategy of prodrug delivery, with its main advantages being represented by an enhanced efficacy and a reduced off-target toxicity of the active drug. In recent years, numerous therapeutic systems based on GDEPT strategy have entered clinical trials. In order to deliver the desired gene at a specific site of action, this therapeutic approach uses vectors divided in two major categories, viral vectors and non-viral vectors, with the latter being represented by chemical delivery agents. There is considerable interest in the development of non-viral vectors due to their decreased immunogenicity, higher specificity, ease of synthesis and greater flexibility for subsequent modulations. Dendrimers used as delivery vehicles offer many advantages, such as: nanoscale size, precise molecular weight, increased solubility, high load capacity, high bioavailability and low immunogenicity. The aim of the present work was to provide a comprehensive overview of the recent advances regarding the use of dendrimers as non-viral carriers in the GDEPT therapy.     

Direct measurement of relative and collective diffusion in a dilute binary colloidal suspension

Experimental characterization of the dynamics of multicomponent fluids is a problem of general importance to the field of complex fluids. We demonstrate a new experimental approach, termed two-color Fourier imaging correlation spectroscopy, which allows direct measurement of the partial dynamic structure factors, S(11)(k,tau), S(22)(k,tau), and S(12)(k,tau), where 1, 2 label the component species of a binary colloidal suspension. Linear combinations of the partial dynamic structure factors yield the characteristic time-correlation functions of the binary fluid. These are the correlation functions of concentration fluctuations S(CC)(k,tau), number density fluctuations S(NN)(k,tau), and cross-correlations between number density and concentration fluctuations S(NC)(k,tau). Test measurements are performed on a dilute symmetric mixture of fluorescently labeled 0.5 and 1.0 microm polystyrene spheres. From these data, we determine generalized collective and relative diffusion coefficients, and compare them to the predictions for an ideal mixture of noninteracting particles.     

Rayleigh scattering fromn=3 states of hydrogenlike atoms

An exact analytic evaluation of the Kramers-Heisenberg matrix elements for Rayleigh scattering fromn=3 states of hydrogenlike atoms is performed in the nonrelativistic dipole approximation, using the Green's function method. The results are given separately for each subshell. The possibility of 3s?3d transitions is also considered. The dependence on the photon energy is contained in six invariant amplitudes. The formulas needed for the evaluation of the various cross sections are presented. The numerical results are contained in tables from which partial and total cross sections can be easily built, covering the energy range from zero up to 20 times theK threshold energy. In the vicinity of Balmerα frequency the cross section is large and comparable with that for excitedn=2 states, confirming an earlier hypothesis of Röhr. At other energies the cross sections forn=2 andn=3 states are comparable, too. The results should be useful in plasma diagnostics.