Screening Papaveraceae as Novel Antibiofilm Natural-Based Agents

The antimicrobial properties of herbs from Papaveraceae have been used in medicine for centuries. Nevertheless, mutual relationships between the individual bioactive substances contained in these plants remain poorly elucidated. In this work, phytochemical composition of extracts from the aerial and underground parts of five Papaveraceae species (Chelidonium majus L., Corydalis cava (L.) Schweigg. and Körte, C. cheilanthifolia Hemsl., C. pumila (Host) Rchb., and Fumaria vaillantii Loisel.) were examined using LC-ESI-MS/MS with a triple quadrupole analyzer. Large differences in the quality and quantity of all analyzed compounds were observed between species of different genera and also within one genus. Two groups of metabolites predominated in the phytochemical profiles. These were isoquinoline alkaloids and, in smaller amounts, non-phenolic carboxylic acids and phenolic compounds. In aerial and underground parts, 22 and 20 compounds were detected, respectively. These included: seven isoquinoline alkaloids: protopine, allocryptopine, coptisine, berberine, chelidonine, sanguinarine, and chelerythrine; five of their derivatives as well as non-alkaloids: malic acid, trans-aconitic acid, quinic acid, salicylic acid, trans-caffeic acid, p-coumaric acid, chlorogenic acid, quercetin, and kaempferol; and vanillin. The aerial parts were much richer in phenolic compounds regardless of the plant species. Characterized extracts were studied for their antimicrobial potential against planktonic and biofilm-producing cells of S. aureus, P. aeruginosa, and C. albicans. The impact of the extracts on cellular metabolic activity and biofilm biomass production was evaluated. Moreover, the antimicrobial activity of the extracts introduced to the polymeric carrier made of bacterial cellulose was assessed. Extracts of C. cheilanthifolia were found to be the most effective against all tested human pathogens. Multiple regression tests indicated a high antimicrobial impact of quercetin in extracts of aerial parts against planktonic cells of S. aureus, P. aeruginosa, and C. albicans, and no direct correlation between the composition of other bioactive substances and the results of antimicrobial activity were found. Conclusively, further investigations are required to identify the relations between recognized and unrecognized compounds within extracts and their biological properties.     

Solvent‐free alkali and alkaline earth metal complexes of di‐imine ligands

Compound [(dph‐BIAN)Mg(THF)]₂ ( 2 ) was prepared by reacting magnesium metal with 1,2‐bis[(2‐biphenyl)imino]acenaphthene (dph‐BIAN) in THF, followed by crystallization from toluene. Reaction of CaI₂ with (dpp‐BIAN)Li₂ in toluene afforded [(dpp‐BIAN)Li]₂Ca ( 3 ) (dpp‐BIAN = 1,2‐bis[(2,6‐diisopropylphenyl)imino]acenaphthene). Both complexes 2 and 3 were characterized by single crystal X‐ray diffraction. The ¹H NMR spectroscopic data obtained for complex 3 in toluene solution indicated an agostic interaction between the methyl groups of the ligand and lithium atoms. © 2005 Wiley Periodicals, Inc. Heteroatom Chem 16:663–670, 2005; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20168     

Curing and properties of chloroprene and butadiene rubber (CR/BR) blends cross-linked with copper(I) oxide or copper(II) oxide

This paper discusses the curing and properties of chloroprene and butadiene rubber (CR/BR) blends cross-linked with copper(I) oxide (Cu₂O) or copper(II) oxide (CuO). The results revealed that the cross-linking degree of CR/BR blends decreased with the increasing amount of butadiene rubber (BR) in the blends. The mechanical properties of cured CR/BR blends depended on the proportion of elastomers in blends, as well as on the type and amount of the cross-linking agent (Cu₂O, CuO). The cross-linking of CR/BR/Cu₂O or CR/BR/CuO blends followed according to cationic mechanism, using Lewis acid, copper(I) chloride (CuCl) or copper(II) chloride (CuCl₂) generated in situ. Additionally, the prepared compositions, both unfilled and filled, were characterized by very high resistance to flame.     

Electron Transfer and Electron Excitation Processes in 2,5-Diaminoterephthalate Derivatives with Broad Scope for Functionalization

Derivatives of 2,5-diaminoterephthalate (DAT) are efficient fluorescence dyes that are also redox-active, thus allowing for the electrochemical manipulation of spectral properties. The electrochemical behaviour of seven DAT derivatives was studied by cyclic voltammetry in dichloromethane. In the absence of a proton donor, DATs should be oxidized in two one-electron steps. The first step is usually quasi-reversible while the second step is either quasi-reversible or irreversible. Some electrochemical properties such as the formal potentials and the ratio between the anodic and the cathodic current were determined from the cyclic voltammograms. Correlation between the formal potential of first oxidation and the absorption or the fluorescence emission wavelengths are established for this specific type of dyes. These correlations were confirmed with density functional theory calculations.     

Stabilisation Effect of Calcium Ions on Polymer Network in Hydrogels Derived from a Lyotropic Phase of Hydroxypropylcellulose

The process of crosslinking of the hydrogel, derived from lyotropic liquid crystalline (LLC) phases of hydroxypropylcellulose/acrylic acid-water, by calcium ions was studied by means of Raman and dielectric spectroscopy. Formation of salt by poly(acrylic acid) and calcium ions, resulting in hydrogel crosslinking, induces differences in Raman spectra of the hydrogel before and after the crosslinking. The crosslinking results in significant increase in the activation energy of β-relaxation of poly(acrylic acid). This is a direct consequence of restriction in motions of carboxylic groups of poly(acrylic acid) due to calcium salt formation. Thus, the crosslinking improves polymer network stability in the hydrogel in the swollen state.     

TiO2–carbon nanotube composites for visible photocatalysts – Influence of TiO2 crystal structure

We investigated the influence of the crystal structure of TiO₂ and the use of different TiO₂ precursors on the properties and photocatalytic activity of carbon nanotube (CNTs)–titania composites. We found that the crystal structure and properties of starting TiO₂ nanomaterial significantly affected the effect of CNTs incorporation on the photocatalytic activity under simulated solar and visible light illumination (simulated solar illumination with UV-blocking filter). In case of significant photocatalytic activity under visible light illumination (anatase TiO₂), likely due to the presence of native defects, composites exhibited lower activity under visible illumination only, but higher activity under simulated solar illumination. The opposite trends were observed for P25 (anatase + rutile) and rutile TiO₂, where incorporation of CNTs resulted in a significant increase of photocatalytic activity under visible illumination. Thus, control over crystal structure and native defects is essential for the development of efficient visible light activated photocatalysts.     

Dual field nonlinear dielectric spectroscopy in a glass forming EPON 828 epoxy resin

Results of the dual field nonlinear dielectric spectroscopy (NDS) studies in supercooled glass forming epoxy resin EPON 828 are presented. For the NDS, changes of dielectric permittivity induced by DC (rectangular) or AC (sine-wave) pulses of a strong electric field were probed by a weak radio frequency electric field. A clear stretched exponential (x < 1) decay after switching off the DC pulse and a single exponential decay (x = 1) after switching off the AC pulse were found. The same results are presented for preliminary studies in superpressed low molecular glass former di-isobutyl phthalate. This observation may be considered as an argument for the heterogeneous picture of supercooled glass forming materials. The temperature dependences of the stationary responses related to DC and AC strong electric field excitations are also shown. The sensitivity of the applied set up made it possible to detect NDS outputs even for electric fields E(strong) < 10 kV cm(-1), qualitatively weaker than in similar 'nonlinear, dielectric' experimental studies on glass forming materials carried out so far.     

Raman light scattering,infrared absorption and DSC studies of the phase transition and vibrational and reorientational dynamics of H2O ligands and ClO4– anions in [Ba(H2O)3](ClO4)2

[Ba(H₂O)₃](ClO₄)₂ between 90 and 300 K possesses two solid phases. One phase transition of the first‐order type at: = 211.3 K (on heating) and = 204.6 K (on cooling) was determined by differential scanning calorimetry. The entropy change value (ΔS ≈ 15 Jmol^–1 K^–1), associated with the observed phase transition, indicates a moderate degree of molecular dynamical disorder. Both, vibrational and reorientational motions of H₂O ligands and ClO₄^– anions, in the high‐temperature and low‐temperature phases, were investigated by Fourier transform far‐infrared and middle‐infrared and Raman light scattering spectroscopies. The temperature dependences of the full‐width at half‐maximum values of the bands associated with ρ_w(H₂O) mode, in both infrared (~570 cm^–1) and Raman light scattering (~535 cm^–1) spectra, suggest that the observed phase transition is not associated with a sudden change of a speed of the H₂O reorientational motions. Ligands reorient fast, with correlation time of the order of several picoseconds, with a mean activation energy value E_a = 5.1 kJ mol^–1 in both high and low temperature phases. On the other hand, measurements of temperature dependences of full‐width at half‐maximum values of the infrared band at ~460 cm^–1, associated with δ_d(OClO)E mode, and Raman band at ~1105 cm^–1, associated with ν_as(ClO)F₂ mode, revealed the existence of a fast ClO₄^– reorientation in phase I and in phase II, with the E_a(I) and E_a(II) values equal to 8.0 and 6.5 kJ mol^–1, respectively. These reorientational motions of ClO₄^– are slightly distorted at the T_C. Fourier transform far‐infrared and middle‐infrared spectra with decreasing of temperature indicated characteristic changes at the vicinity of PT at T_C, which suggested lowering of the crystal structure symmetry. All these experimental facts suggest that the discovered phase transition is associated with small change of H₂O ligands and somewhat major change of ClO₄^– anions reorientational dynamics, and with insignificant change of the crystal structure, too. Copyright © 2012 John Wiley & Sons, Ltd.     

Nature of versatile chemisorption on TiC(111) and TiN(111) surfaces

Density-functional calculations on the polar TiX(111) (X = C, N) surfaces show (i) for clean surfaces, strong Ti3d-derived surface resonances (SR’s) at the Fermi level and X2p-derived SR’s deep in the upper valence band and (ii) for adatoms in periods 1-3, pyramidic trends in atomic adsorption energies, peaking at oxygen (9 eV). A concerted-coupling model, where adatom states couple to both kinds of SR’s in a concerted way, describes the adsorption. The chemisorption versatility and the general nature of the model indicate ramifications and predictive abilities in, e.g., growth and catalysis.     

BaHfO3:Ce sintered ceramic scintillators

Raw powders of BaHfO₃:Ce were prepared with modified Pechini process and were calcined in the 650–1700 °C range of temperatures, at different atmospheres – air, vacuum and nitrogen–hydrogen mixture. The powders were converted into sintered ceramics by vacuum sintering. The materials were characterized by XRD, TEM, photoluminescence and radioluminescence spectroscopy. UV-VUV excitation spectra were recorded using synchrotron radiation. Excitation spectra proved that atmosphere of preparation significantly influences the host-to-activator energy transfer, which is the most efficient for materials made in reducing conditions. Also radioluminescence efficacy was found to be superior for materials prepared in such conditions.