Evaluation of translational friction coefficients of macroscopic probes in nematic liquid crystals

We present a study of the translational friction coefficients of spherical and ellipsoidal probes in nematic liquid crystalline fluids, based on the numerical treatment of Leslie-Ericksen equations [Q. J. Mech. Appl. Math. 19, 357 (1966); Adv. Liq. Cryst. 4, (1979); Trans. Soc. Rheol. 5, 23 (1961); Adv. Liq. Cryst. 2, 233 (1976)] for incompressible nematic fluids. Simulations of director dynamics in a local environment surrounding the moving probe are presented, and the dependence of translational diffusion on liquid crystal viscoelastic parameters is discussed. The time evolution of the director field is studied in the presence of an orienting magnetic field in two characteristic situations: Directors of motion parallel and perpendicular with respect to the field. In the particular case under investigation, a detailed analysis is given for the case of spherical, prolate, and oblate ellipsoidal probes in rectilinear motion in nematic (4-methoxibenzylidene-4'-n-butylaniline), together with a comparison with other nematogens, namely, 4,4'-dimethoxuazoxy benzene and (4'-n-pentyl-4-cyanobiphenil). A discussion of the general methodology presented in this work is given for the case of colloidal dispersions in nematic liquid crystals, which are considered as model systems of dispersions of particles in host media with anisotropic physical properties.     

The Square of Opposition and the Four Fundamental Choices

Each predicate of the Aristotelian square of opposition includes the word “is”. Through a twofold interpretation of this word the square includes both classical logic and non-classical logic. All theses embodied by the square of opposition are preserved by the new interpretation, except for contradictories, which are substituted by incommensurabilities. Indeed, the new interpretation of the square of opposition concerns the relationships among entire theories, each represented by means of a characteristic predicate. A generalization of the square of opposition is achieved by not adjoining, according to two Leibniz’ suggestions about human mind, one more choice about the kind of infinity; i.e., a choice which was unknown by Greek’s culture, but which played a decisive role for the birth and then the development of modern science. This essential innovation of modern scientific culture explains why in modern times the Aristotelian square of opposition was disregarded. This work was completed with the support of our -pert.     

XPS and AFM characterization of the enzyme glucose oxidase immobilized on SiO(2) surfaces

A process to immobilize the enzyme glucose oxidase on SiO2 surfaces for the realization of integrated microbiosensors was developed. The sample characterization was performed by monitoring, step by step, oxide activation, silanization, linker molecule (glutaraldehyde) deposition, and enzyme immobilization by means of XPS, AFM, and contact angle measurements. The control of the environment during the procedure, to prevent silane polymerization, and the use of oxide activation to obtain a uniform enzyme layer are issues of crucial importance. The correct protocol application gives a uniform layer of the linker molecule and the maximum sample surface coverage. This result is fundamental for maximizing the enzyme bonding sites on the sample surface and achieving the maximum surface coverage. Thin SiO2 layers thermally grown on a Si substrate were used. The XPS Si 2p signal of the substrate was monitored during immobilization. Such a signal is not completely shielded by the thin oxide layer and it is fully suppressed after the completion of the whole protocol. A power spectral density analysis on the AFM measurements showed the crucial role of both the oxide activation and the intermediate steps (silanization and linker molecule deposition) to obtain uniform immobilized enzyme coverage. Finally, enzymatic activity measurements confirmed the suitability of the optimized protocol.     

Self-propagating assembly of a molecular-based multilayer

Accelerated growth of a molecular-based material that is an active participant in its continuing self-propagated assembly has been demonstrated. This nonlinear growth process involves diffusion of palladium into a network consisting of metal-based chromophores linked via palladium.     

Reactive oxygen species scavenging activity of flavone glycosides from Melilotus neapolitana

One new and six known flavone glycosides were isolated from the MeOH extract of Melilotus neapolitana Ten. The new compound, identified as 7-O-beta-D-glucopyranosyloxy-4',5-dihydroxy-3-[O-alpha-L-rhamnopyranosyl-(1-->6)-3-O-beta-D-glucopyranosyloxy]flavone (1) by 1D and 2D NMR techniques and mass spectra, was isolated along with kaempferol-3-O-rutinoside (2), kaempferol-3-O-glucoside (3), rutin (4), quercetin-3-O-glucoside (5), isorhamnetin-3-O-rutinoside (6), and isorhamnetin-3-O-glucoside (7). The antioxidant and radical scavenging activities of these compounds and the whole crude methanol extract were evaluated. The organic extract can inhibit MDA marker's synthesis by 57%. All the metabolites displayed good reducing power, with the kaempferol (2,3) and isorhamnetin derivatives (6,7) being less active than the corresponding quercetin derivatives 4,5.     

DNA and RNA noncovalent interaction of platinum(II) polypyridine complexes

A comparative investigation of the noncovalent interaction of the platinum(II) polypyridine complexes [Pt(dipy)(n-Rpy)2]2+ and [Pt(4,4'-Me2dipy)(2-Rpy)2]2+ (dipy = 2,2'-dipyridine; Me = CH3; n = 2-4; R = H or CH3) with double-helical DNA (calf thymus) and RNA [poly(A).poly(U)] has been conducted. With the exception of [Pt(dipy)(2-Mepy)2]2+, all of the complexes interact strongly, by intercalation, with both nucleic acids giving rise to large changes in the electronic spectra and induced circular dichroism signals; in addition, viscosity experiments on rodlike DNA and RNA show that both biopolymers elongate upon interaction with the complexes. The binding constant values, KB, determined at 25 degrees C, indicate that, at 0.101 M ionic strength, the affinity for poly(A).poly(U) is strongly dependent on the complexes nature, while for DNA it is leveled off. [Pt(dipy)(2-Mepy)2]2+ binds to DNA but does not interact appreciably with poly(A).poly(U).     

Analysis of Composites with Infrared Thermography

The aim of this study was a non-destructive evaluation of composites through their behaviour under thermal stimulation. Such behaviour was monitored by infrared thermography. Several specimens were fabricated involving: glass/epoxy with inclusion of foreign materials; carbon/epoxy with backdrilled holes; carbon/epoxy with impact damage; Glare^® failed in bearing way. The obtained results prove that infrared thermography is capable of detecting the materials inhomogeneities and/or damage listed above. In particular, lock-in thermography is capable of supplying useful information about: the distribution of the adhesive thickness in composite structures; the distribution of the paint thickness; the behaviour under load of aluminium layers and glass fibres in Glare^®.     

Diethylbis(2,2′‐bipyridine)iron/MAO. A Very Active and Stereospecific Catalyst for 1,3‐Diene Polymerization

Diethylbis(2,2′‐bipyridine)Fe/MAO is an extremely active catalyst for the polymerization of 1,3‐dienes. Polymers with a 1,2 or 3,4 structure are formed from butadiene, isoprene, (E)‐1,3‐pentadiene and 3‐methyl‐1,3‐pentadiene, while cis‐1,4 polymers are derived from 2,3‐dimethyl‐1,3‐butadiene. The 1,2 (3,4) polymers obtained at 25°C are amorphous, while those obtained below 0°C are crystalline, as was determined by means of X‐ray diffraction. Mechanistic implications of the results are briefly discussed.