Proton double quantum coherence and cross-relaxation in (NH4)2SnBr6

A proton double quantum coherence signal can be observed exclusively from the T species NH4 groups (with the total spin I = 1) in ammonium compounds at low temperatures by the three-pulse sequence 90x degrees - tpr - 90x degrees - tev - 90x degrees - ta, where tpr and ta are of the magnitude of the inverse line width and tev very short. The usefulness of this pulse sequence, preceded by the additional pulse sequence 90x degrees - t1 -90(-x) degrees - t2 for creating an unbalance between the A and T species magnetizations, was demonstrated by applying it to cross-relaxation studies in (NH4)2SnBr6.     

O 1s --> sigma* resonance in O2: inadequacy of only two exchange-split components

The O 1s-->sigma* transition below the O K-edge in O2 has been investigated by absorption, constant ionic state (CIS) experiments, and extensive configuration interaction calculations. CIS scans of the three lowest-lying final states reached in resonant Auger decay provide a wealth of information on energy range, symmetry, and spin multiplicity of the intermediate states with sigma* character. We conclude that the identification of only two exchange-split components is inadequate because a complex manifold of states with sigma* character exists with no unique energy difference between related states.     

Vibrational frequencies,infrared absorption intensities and energy differences between rotational isomers of propyl halides

Infrared absorption intensities of fundamental bands of propyl halides n-C₃ H₇ Cl, n-C₃H₇ Br and n-C₃H₇I were measured in the pure liquid state. In order to obtain L matrix data necessary for the intensity computation, normal frequencies of the rotational isomers were calculated, and LSFF force constants were determined by the least squares method so as to attain the best fit between the observed and calculated frequencies. By applying the absolute intensity method, energy differences between the rotational isomers were evaluated, which are in quite good agreement with values obtained by the temperature variation method.     

Rapidity density distributions in antiproton-proton collisions

Data on the density of charged particles in rapidity space for annihilation and non-annihilation p?p interactions at 7.3 and 12 GeV/c are reported. It is shown that the central rapidity density for non-annihilation processes is a simple linear function of $\text{ln}\text{(}\text{s}\text{)}$ from these low energies up to p?p collider energies ($\text{s}\text{=540}\text{GeV}$). Significant differences in density distributions for p?p and e^?e⁺ annihilations at comparable energies are found.     

The standard model on non-commutative space-time: strong interactions included

This paper is a direct extension of our earlier work on electroweak currents and the Higgs sector in the standard model on non-commutative space-time, now with strong interactions included. Apart from the non-commutative corrections to standard model strong interactions, several new interactions appear. The most interesting ones are gluonic interactions with the electroweak sector. They are elaborated here in detail and the Feynman rules for interactions up to are provided.Received: 18 March 2005, Revised: 13 May 2005, Published online: 19 July 2005     

Quantitative plasma determination of a novel antiretroviral derivative of zidovudine by solid-phase extraction and high-performance liquid chromatography

A solid-phase extraction methodology, followed by high-performance liquid chromatography (HPLC) quantification with UV absorbance detection (λ=267 nm), was developed in order to study the stability of 3′-azido-3′-deoxy-5′-O-isonicotinoylthymidine (AZT-Iso), a novel derivative of the antiretroviral AZT, in different matrixes. The half-lives (t _1/2) for AZT-Iso were 1.19, 1.13 and 0.30 h for human, rat and rabbit plasma, respectively, and 14.91 and 25.49 h for potassium phosphate buffer (pH 7.4) and human serum albumin solution, respectively. The HPLC method proved to be selective, sensitive and accurate. Good recovery, linearity and precision were achieved using p-fluorophenol as an internal standard. The validity of this method was tested using synthetic mixtures of the intact drug with its decomposition products. In conclusion, the method presented is applicable to in vivo pharmacokinetics studies of AZT-Iso in rats.     

Structural rearrangements and magic numbers in reactions between pyridine-containing water clusters and ammonia

Molecular cluster ions H(+)(H(2)O)(n), H(+)(pyridine)(H(2)O)(n), H(+)(pyridine)(2)(H(2)O)(n), and H(+)(NH(3))(pyridine)(H(2)O)(n) (n = 16-27) and their reactions with ammonia have been studied experimentally using a quadrupole-time-of-flight mass spectrometer. Abundance spectra, evaporation spectra, and reaction branching ratios display magic numbers for H(+)(NH(3))(pyridine)(H(2)O)(n) and H(+)(NH(3))(pyridine)(2)(H(2)O)(n) at n = 18, 20, and 27. The reactions between H(+)(pyridine)(m)(H(2)O)(n) and ammonia all seem to involve intracluster proton transfer to ammonia, thus giving clusters of high stability as evident from the loss of several water molecules from the reacting cluster. The pattern of the observed magic numbers suggest that H(+)(NH(3))(pyridine)(H(2)O)(n) have structures consisting of a NH(4)(+)(H(2)O)(n) core with the pyridine molecule hydrogen-bonded to the surface of the core. This is consistent with the results of high-level ab initio calculations of small protonated pyridine/ammonia/water clusters.