Adsorption of isoniazid onto sepiolite–palygorskite group of clays: An IR study

The adsorption of isoniazid (INH) on sepiolite, loughlinite (natural Na-sepiolite) and palygorskite from Anatolia was investigated by FT-IR spectroscopy. Experimental results indicated that INH molecules, adsorbed on sepiolite–palygorskite group of clays, are coordinated to surface hydroxyls by H-bonding interaction through the pyridine ring nitrogen lone pairs. Moreover, some of the adsorbed INH molecules may enter the interior channels of the sepiolite–palygorskite structure and involve H-bonding interaction with zeolitic water. Some intensity and frequency changes in the OH stretching band of surface hydroxyls (Si–OH) of the INH-treated sepiolite and loughlinite were observed. However, this band is found to be less affected by the adsorption of isoniazid in the case of palygorskite, probably because the surface Si–OH groups in palygorskite appear to be less abundant than in sepiolite or loughlinite.     

IR spectroscopic studies on the transmission of substituent effects to carbonyl and thiocarbonyl stretching frequencies in 4-substituted phenyl-4,5-dihydrobenzo [f] [1,4] oxazepin-3 (2H)-ones (thiones)

Single and dual substituent correlation analysis were applied to study transmission of substituent effects on IR carbonyl and thiocarbonyl stretching frequencies of 4-substituted phenyl-4,5-dihydrobenzo [f] [1,4] oxazepin-3 (2H)-ones (5a–n) and -thiones (6a–n). The substituent effects were estimated on the basis of results of the statistical analysis. The differences among the regression coefficients were discussed in terms of the relative importance of the substituent field and resonance effects. For a better understanding of the results, density functional theory (DFT) calculations were performed to determine the preferred geometry and to calculate the theoretical carbonyl and thiocarbonyl stretching frequencies.     

Synthesis of electroluminescent copoly(aryl ether)s containing alternate 1,4‐distyrylbenzene derivatives and aromatic 1,3,4‐oxadiazole or 3,3″‐terphenyldicarbonitrile segments

New copoly(aryl ether)s ( P1 – P3 ) containing alternate 2,5‐dihexyloxy‐1,4‐di(m‐ethoxystyryl)benzene ( P1 , P2 ) or 2,5‐dihexyloxy‐1,4‐distyrylbenzene ( P3 ) chromophores and aromatic 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) segments were prepared by Horner reaction ( P1 and P2 ) or nucleophilic displacement reaction ( P3 ). They are basically amorphous materials with 5% weight‐loss temperature above 410 °C. Their absorption, photoluminescence spectra, and quantum yields are dependent on the composition of the isolated fluorophores. The emissions are exclusively dominated by 1,4‐distyrylbenzene segments via excitation energy transfer from electron‐transporting 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) chromophores. The HOMO and LUMO energy levels have been estimated from their cyclic voltammograms, and the observations confirm that oxidation and reduction start from the emitting 1,4‐distyrylbenzene and electron‐transporting segments, respectively, indicating that both carriers affinity can be enhanced simultaneously. Among the two‐layer PLED devices (ITO/PEDOT/ P1 – P3 /Al), P1 exhibits the best performance with a turn‐on field of 4 × 10⁵ V/cm and a maximum luminance of 225 cd/m². However, P2 emits green–yellow light (555 nm), owing to the excimer emission. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5009–5022, 2005     

Synthesis of potential inhibitors of glycosyltransferases representing UDP-GlcNAc

Based on rational design of the transition state analog inhibitors of glycosyltransferases, four model glycomimetics of this type, viz. benzyl 2-thio-α-dfructofuranoside 1-diethylphosphate (XIa), its β-anomer (XIb), and their ethyl 2-thio analogs — α-anomer (XIIa) and β-anomer (XIIb), were synthesized. In addition, fourteen precursors arising during the synthesis of the desired final model compounds (XI and XII), partially or fully acetylated benzyl and/or ethyl 2-thiofructofuranoside 1-diethyl phosphates, were isolated and characterized with the aim to prepare complete series of glycomimetics, representing donor UDP-GlcNAc designated for biological assays on human GnT’s, viz. GnT-I, Core2GnT, and GnT-V.     

Anti-Quorum Sensing and Anti-Biofilm Activity of Pelargonium × hortorum Root Extract against Pseudomonas aeruginosa: Combinatorial Effect of Catechin and Gallic Acid

HPLC-UV was used to compare the major constituents of two Pelargonium × hortorum cultivars and Pelargonium sidoides root extract. It revealed the presence of catechin and gallic acid in high concentrations and the absence of umckalin in P. × hortorum root extracts. The antibacterial activity of these extracts was screened against 19 Pseudomonas aeruginosa clinical isolates. P. × hortorum root extracts showed the lowest MIC values (512–1024 µg/mL). This activity was concluded to be attributable to the high concentrations of catechin and gallic acid. The anti-biofilm activity of catechin, gallic acid, and their combination was examined by a crystal violet assay. The combination reduced the percentage of strong and moderate biofilm-forming isolates from 52.63% to 5.26%. The impact on lasI and lasR genes expression using qRT-PCR and simultaneous docking against LasR protein was explored. The combination downregulated lasI and lasR gene expression in eight and six P. aeruginosa isolates, respectively, and showed the greatest docking score. Additionally, the in vivo protection capability of this combination in infected mice showed enhancement in the survival rate. Our study revealed the potential biofilm and quorum-sensing-inhibitory activity of the catechin and gallic acid combination as a novel alternative to inhibit bacterial pathogenicity.     

Acousto-optic mode-locker for Nd:Lasers using paratellurite

The design of an acousto-optic modulator using paratellurite requiring only low driving power is described. Because of the high figure of merit a high modulation index can be achieved. To avoid an intermediate transmission peak the modulator should not be operated in the Bragg-regime but rather in the transition regime. The time dependent transmission for this regime is calculated as a function of the material parameters. Experimentally, modulation indices up to 10 are obtained. Using such a TeO₂ mode-locker a pulsed Nd:Cr:GSGG laser delivered pulses down to 70 ps.     

Use of 13C isotope shifts for assignment of deuterium labelling sites in 1,3-diphenylpropan-1-one

¹³C NMR spectroscopy was used for the unequivocal analysis of the mixture of products of RuCl₂[P(C₆H₅)₃]₃-catalysed transfer deuteriation of benzylideneacetophenone by (a) DCOONa/H₂O, (b) HCOONa/D₂O and (c) DCOONa/D₂O. Signal assignments in the ¹³C spectra were obtained mainly from the deuterium-induced ¹³C isotope shifts. The geminal ¹³C? ²H shift of the β-carbon of deuteriated 1,3-diphenylpropan-1-one is almost twice that for the α-carbon.     

Identification of hidden variables through Everett’s formalism

It is well known that the conventional interpretation of quantum mechanics entails several paradoxes which have not been resolved in a complete and convincing way. To avoid these paradoxes other interpretations were suggested and advances, among which were the “hidden variables” theory (HV) of Bohm and Bub [1], and the “relative state” theory of Everett [2]. These HV have not, up to now, been identified, but if we compare these theories we can show an equivalence between them, and arrive at a possible definition of the HV.