The use of water-soluble phthalocyanines as textile dyes in nylon/elastane fabric: fastness and antibacterial effectiveness

This work reports on dyeing of nylon/elastane fabric with water-soluble phthalocyanines ( 1-4 ) bearing quinoline 5-sulfonic acid substituents on the peripheral or nonperipheral positions and determining the antibacterial efficiency of the phthalocyanine compounds and the dyed nylon/elastane fabrics. The light, washing, water, perspiration, and rubbing fastness properties of nylon/elastane fabrics dyed with phthalocyanines were also determined. The results showed that all dyed fabrics showed very good wet fastness values. The lightfastness value of the nylon/elastane fabric dyed with phthalocyanine dye ( 1 ) showed a much better value than the others. Also, the antibacterial efficiencies of the dyed nylon fabrics and the dye compounds were investigated against a gram-negative ( Escherichia coli ) and a grampositive ( Staphylococcus aureus ) bacteria by using disc diffusion method. The results showed that the dyed nylon/elastane fabrics and the compounds exhibited antibacterial activities against both bacteria.     

Low-frequency scattering by rectangular dielectric particles

The field scattered by a homogeneous isotropic dielectric particle illuminated by a low-frequency plane electromagnetic wave is expressed in terms of a single polarizability tensor which is a function of only the geometry of the particle and a material parameter τ representing either the relative permittivity or permeability of the dielectric. The mathematical formulation is specialized to the case of a rectangular parallelepiped and numerical techniques are developed for computing the tensor elements. Specific data are presented for the tensor elements of rectangular parallelepipeds having square cross sections and are compared to the results obtained for spheroids and right circular cylinders of similar dimensions.     

Elektrolytische Apparate

Ohne Zusammenfassung     

Bio-effects of high magnetic fields: a study using a simple animal model.

The desire to do clinical imaging and spectroscopy at magnetic field strengths greater than 2 Tesla (T) necessitates investigation of possible bioeffects at these high fields. A simple T-maze was utilized to evaluate the aversive effects of exposure to three levels of static magnetic field (0, 1.5, and 4 T). The right arm of the maze extended into the center of a 30-cm horizontal bore magnet, while the left arm extended into a mock magnet bore with the same dimensions. The self-shielded design of the magnet reduces the fringe field to zero within 1 m of the bore, placing the start box of the maze outside the 5-G line of the magnet. Each rat performed a total of ten trials at each level of magnetic field strength. A follow-up subset was run at 4 T with the maze reversed. At 0 T, the rats entered the magnet freely. No significant differences from the control were observed at 1.5 T. At 4 T, however, in 97% of the trials the rats would not enter the magnet. In the maze-reversed subset a majority of the rats turned toward the magnet, indicating that they had learned an aversive response from the previous trials at 4 T. However, in only 4 decisions out of 58 did the rats actually enter the magnet. Eighteen decisions to turn around were made at the edge of the magnet in a region of strong field gradients (up to 13 T/m) and a field strength up to 1.75 T.(ABSTRACT TRUNCATED AT 250 WORDS)     

Dual-beam holographic deflection measurement

Deflection is recorded at different sensilivities over a limited portion of the holographic range by introducing equal but opposite phase changes into the holograms created by a dual-beam illumination. The technique does not require a partially reflecting mirror, patterns can be optically filtered for better fringe contrast and in-plane displacement can be recorded without making any modifications in the experimental setup. Results obtained from two-and three-dimensional surfaces agree well with theory and verify analytical arguments presented throughout the paper.     

Synthesis of dimeric Re(I) amino acid conjugate complexes

The aqueous one-step reaction of Re(CO)(3)(H(2)O)(3)(+) with pyridine-2-carboxyaldehyde and glycine or alanine produces a new class of cyclic dimeric products. The ligands of the chiral C(2)-symmetric products are bound via the diimine at one rhenium centre and via the pendant carboxylate to a second rhenium center.     

A one-step conversion of esters to secondary alcohols with LiBH4-RMgX

A one-pot synthesis of secondary alcohols from esters and LiBH₄-RMgX is described.     

Total Syntheses of Xiamycins A,C, F,H and Oridamycin A and Preliminary Evaluation of their Anti‐Fungal Properties

Divergent and enantiospecific total syntheses of the indolosesquiterpenoids xiamycins A, C, F, H and oridamycin A have been accomplished. The syntheses, which commence from (R)‐carvone, employ a key photoinduced benzannulation sequence to forge the carbazole moiety characteristic of these natural products. Late‐stage diversification from a common intermediate enabled the first syntheses of xiamycins C and F, and an unexpected one‐pot oxidative decarboxylation, which may prove general, led to xiamycin H. All synthetic intermediates and the natural products were tested for anti‐fungal activity. Xiamycin H emerged as an inhibitor of three agriculturally relevant fungal pathogens.     

Rearrangement of 3-membered 1,1,2-trifluorobromonium and iodonium ions and comparison of trifluorochloronium to fluorocarbenium ions

Reactions of chlorine (Cl(2)) with 4-halo-1,1,2-trifluorobut-1-enes (1, 2, or 3) give open-ion intermediates A and E that are in equilibrium. The open-chloronium ions (E) rearrange to a five-membered-ring halonium ion during ionic chlorination of 3 when the number-4 halo-substituent is iodine. Three-membered-ring bromonium and iodonium ions from alkenes 1, 2, or 3 are rather symmetrical and similar in structure. Quantum chemical calculations show that five-membered-ring halonium ion intermediates are 11 to 27 kcal/mol more stable than the three-membered-ring halonium ions or the open-ions A and E. The five-membered-ring intermediates lead to rearranged products. Rearranged products increase as the number-4 halogen (Z) becomes more nucleophilic (Z: Cl < Br < I). Open chloronium ions from ionic chlorination of terminal fluorovinyl alkenes are compared to the open ions generated by protons to similar alkenes.     

Synthesis of tungsten compounds with Schiff base ligands prepared from ferrocenecarboxaldehyde: Observation of the migration of an imine double bond

The one-pot reactions of ferrocenecarboxaldehyde, W(CO)₄(pip)₂ (pip = piperidine) and either 2-(aminomethyl)pyridine or 2-(2-aminoethyl)pyridine lead to clean formation of pyridine imine products W(CO)₄(η²-NC₅H₄CHNCH₂C₅H₄FeCp) (1) and W(CO)₄(η²-NC₅H₄C₂H₄NCHC₅H₄FeCp) (2), respectively. Crystal structures of the two compounds show that in 1 the imine double bond has migrated so that it is conjugated with the pyridine ring while in 2 the imine double bond remains conjugated with the cyclopentadienyl ring. This finding is reinforced by a comparison of dihedral angles in each molecule. IR, NMR and electronic spectra each highlight the differences between the two compounds. Crystal data for C₂₁H₁₆FeN₂O₄W (1): monoclinic P2(1)/c, a = 12.768(2) Å, b = 13.593(2) Å, c = 12.981(2) Å, β = 119.46°, V = 1961.6(4) Å³, Z = 4; C₂₂H₁₈FeN₂O₄W (2): monoclinic P2(1)/c, a = 16.759(1) Å, b = 8.8612(7) Å, c = 13.802(1) Å, β = 95.998(1)°, V = 2038.4(3) Å³, Z = 4.