Two-dimensional on- and off-resonance nutation FFT/MEM NQR spectroscopy

The new two-dimensional nuclear quadrupole resonance experiments based on the principle of nutation spectroscopy, which can be used to determine the asymmetry parameter, and thus the full quadrupolar tensor of spin-3/2 nuclei at zero applied magnetic field are discussed. The problems of reconstructing 2D-nutation NQR spectra using conventional methods and the advantages of using implementation of the maximum entropy method (MEM) are analyzed. Use of the MEM in 2D-NQR spectroscopy can lead to sensitivity improvement, reduction of instrumental artifacts and truncation errors, shortened data acquisition times and automatic suppression of noise, while at the same time increasing the resolution. The possibilities of off-resonance irradiation in nutation experiments are demonstrated experimentally and theoretically. It is shown that the off-resonance nutation spectroscopy is a useful extension of the conventional on-resonance experiments thus facilitating the determination of asymmetry parameters in multiple spectrum. The methods have been successfully demonstrated for the³⁵Cl on-and off-resonance 2D-nutation spectra in polycrystalline 2,4,6-trichloro-1,3,5-triazine.     

Acid-catalyzed Hydrolysis of the cis-[Cr(1,10-phenanthroline)2(O2CO)]+ Ion Studied by the u.v.–vis Stopped Flow Method

The cis-[Cr(phen)₂(O₂CO)]⁺ ion was prepared through the displacement of two molecules of water from the cis-[Cr(phen)₂(OH₂)₂]³⁺ by the bidentate carbonate anion. It underwent two-phase hydrolysis reactions under acidic conditions (0.1 < [H⁺] < 2.7 m) at 5, 10, 15, 20 and 25 °C. Via slow carbonato chelate ring opening (first step k₁^slow) and a second fast decarboxylation(k₂^fast value). The first step was preceded by protonation of the coordinate bidentate carbonate ligand. The second step exhibited no pH dependence, while k₁^slow values increased with acid concentration that suggested the presence of both protonated and deprotonated reactant species. Based on these observations we have proposed a hydrolysis mechanism featuring H₂O-induced ring-opening of the coordinate CO₃²⁻ group in the first step k₁^slow followed by loss of CO₃²⁻ from two intermediates, [Cr(phen)₂(O₂COH)]²⁺ (k₁^slow) and [Cr(phen)₂(OH₂)(O₂COH)]²⁺ (k₂^fast).     

Observation of the beam-size effect at HERA

A precise measurement of the spectrum of the photons fromep bremsstrahlung with the ZEUS luminosity monitor at HERA is reported. The measurement shows a reduced rate compared to the Bethe-Heitler spectrum for photon energies below 5 GeV. This suppression, called the beam-size effect, is explained by the finite transverse size of the beam overlap relative to the typical impact parameter in the process ofep bremsstrahlung at HERA energies.piotrzkowski@desy.de     

Amphiphilic block and statistical siloxane copolymers with antimicrobial activity

Statistical and block all‐siloxane copolymers containing quaternary ammonium salt (QAS) groups with biocidal activity as lateral substituents were synthesized as models for the study of the effect of the arrangement of the QAS groups in the copolymer chain on their antimicrobial activity. The bioactive siloxane unit was [3‐n‐octyldimethylammoniopropyl]methylsiloxane, and the neutral unit was dimethylsiloxane. The copolymers also contained siloxane units with unreacted precursor 3‐chloropropyl or 3‐bromopropyl groups. A small number of units containing highly hydrophilic 3‐(3‐hydroxypropyl‐dimethylammonio)propyl groups were introduced to increase the solubility of the copolymers in water. The bioactive and bioneutral units were arranged in the polymer chain either in blocks or in statistical order. The block copolymers differed in the number and length of segments. The copolymers were obtained by the quaternization of tertiary amines by chloropropyl or bromopropyl groups attached to polysiloxane chains. The arrangement of the bioactive groups was controlled by the arrangement of the halogenopropyl groups in the bioactive copolymer precursor. All model siloxane copolymers showed high bactericidal activity in a water solution toward the gram‐negative bacteria Escherichia coli and the gram‐positive bacteria Staphylococcus aureus. However, no essential differences in the activities of the copolymers with block and statistical arrangements of units were detected. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2939–2948, 2003     

Retention Data for Some Carbonyl Derivatives of Imidazo[2,1-c][1,2,4]triazine in Reversed-Phase Systems in TLC and HPLC and their Use for Determination of Lipophilicity. Part 1. Lipophilicity of 8-Aryl-3-phenyl-6,7-dihydro-4H-imidazo[2,1-c][1,2,4]triazin-4-ones

JPC – Journal of Planar Chromatography – Modern TLC - Thirteen carbonyl derivatives of imidazo [2,1-c][1,2,4]triazine have been synthesized as a new bioactive set of substances....     

ATRP of butyl acrylates from functionalized carbon black surfaces

The functionalization of carbon black surface with atom transfer radical polymerization (ATRP) initiating sites and subsequent ATRP of n‐butyl acrylate (n‐BA) and t‐butyl acrylate (t‐BA) from the surface of carbon black is reported. The polymerizations were carried out using CuBr/N,N,N′,N″,N″‐pentamethyldiethylenetriamine as the primary catalytic system in anisole at 70 °C. The initiator density on carbon black surface was tuned and the effect of initiator density on the polymers grafted on the surface was illustrated. Polymerizations were also performed in the presence of a sacrificial initiator to indirectly monitor the molecular weight evolution of polymers formed in the system. Block copolymerization of t‐BA initiated from poly(n‐BA) grafted carbon black was conducted to achieve water‐dispersible carbon black composites after cleavage of the t‐butyl groups. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4695–4709, 2005