Hybrid triple quadrupole-linear ion trap mass spectrometry in fragmentation mechanism studies: application to structure elucidation of buspirone and one of its metabolites

The use of a hybrid triple quadrupole-linear ion trap (QqQ(LIT)) mass spectrometer system for a comprehensive study of fragmentation mechanisms is described. The anxiolytic drug, buspirone, was chosen as a model compound for this study. With the advent of a QqQ(LIT) instrument, both the traditional quadrupole and the new linear ion trap scans (LIT) could be performed in a single LC run. In the past, a sample had to be run on two different instruments, namely, a triple quadrupole instrument (QqQ) and a 3D ion trap (3D IT) to obtain similar information. With the new QqQ(LIT) technology, collision-induced dissociation (CID) occur in a quadrupole collision cell, q2, and fragment ions are trapped and analyzed in Q3 operated in LIT mode. In this work, high-sensitivity product ion spectra of buspirone were obtained from the one-stage 'Enhanced Product Ion' scan (EPI) with rich product ions and no low mass cut-off. Furthermore, detailed fragmentation pathways were elucidated by further dissociation of each of the fragment ions in the EPI spectrum using MS(3) mode in the same run. The MS(3) scan was performed by incorporating CID in q2, and trapping, cooling, isolation, and resonance-excitation in Q3 when operating in LIT mode. This approach allowed unambiguous assignment of all fragment ions quickly with fewer experiments and easier interpretation than the previous approach. The overall sensitivity for obtaining complete fragment ion data was significantly improved for QqQ(LIT) as compared with that of QqQ and 3D IT mass spectrometers. This is beneficial for structure determination of unknown trace components. The method allowed structure determination of metabolites of buspirone in rat microsomes at 1 microM concentration, which was a 10-fold lower concentration than was needed for QqQ or 3D IT instruments. The QqQ(LIT) instrument provided a simple, rapid, sensitive and powerful approach for structure elucidation of trace components.     

Relativistic Hamiltonian dynamics and few-nucleon systems

We present a preliminary calculation of the electromagnetic form factors of ³He and ³H, performed within the light-front Hamiltonian dynamics. Relativistic effects show their relevance even at the static limit, increasing at higher values of momentum transfer, as expected.     

Heterocyclic rearrangements in constrained media. A zeolite-directed photorearrangement of 1,2,4-oxadiazoles

[reaction: see text] The first intrazeolite-photoinduced rearrangement of a five-membered heterocycle is reported. A completely different behavior compared to solution irradiations has been observed. The zeolite's role in directing the photoreaction of 3-phenyl-1,2,4-oxadiazoles toward the formation of the corresponding 1,3,4-oxadiazoles in a ring contraction-ringexpansion route is discussed.     

Low frequency transport measurements in

Low frequency transport measurements are performed on GdSr₂RuCu₂O₈ pellets. The observed current-voltage curves are qualitatively explained in the framework of a simple phenomenological model accounting for coexistence in the sample of ferromagnetism and superconductivity. A Curie temperature T _cM = 133 K and a superconducting critical temperature T _cS = 18 K, with an onset temperature T _cO = 33 K, are extracted from the analysis of the current-voltage curves. Received 18 September 2002 Published online 4 February 2003 RID="a" ID="a"e-mail: canio@sa.infn.it     

Statistical mechanical model for diffusion of simple penetrants in polymers. I. Theory

Following Di Benedetto it is proposed that noncrystalline polymer regions possess an approximate semicrystalline order with chain bundles that are locally parallel along distances of several nanometers. Packing with on-average four nearest neighbors is assumed. A spherical molecule may move through such a substrate in two distinct ways: (a) along the axis of a “tube” formed by locally parallel chains or (b) perpendicular to this axis by two polymer chains separating sufficiently to permit passage of the molecule. The first process is relatively fast, generally requires little activation energy, and determines the effective jump length in diffusion. The second is responsible for the activation energy of diffusion, which is taken as the minimum energy necessary to produce a symmetrical chain separation which allows transfer of a molecule. This is calculated as a function of the penetrant diameter d and parameters Γ and β which characterize the interchain cohesion and chain stiffness, respectively. Γ is estimated from the polymer density and cohesive energy density by suitably linearizing a relation given by Di Benedetto for the potential between two polymer chains approximated as infinite strings of Lennard-Jones force centers. β is shown to be approximately obtainable from the polymer chain backbone geometry and bond rotation potentials. An expression for the diffusion coefficient D is developed which contains only one disposable parameter, the effective jump length.     

Statistical mechanical model for diffusion of simple penetrants in polymers. III. Applications—vinyl and related polymers

The theory developed in Part I of this series is modified to accommodate polymers that possess closely spaced, bulky side groups on the chains. The side groups give rise to free space between the chain “cores,” which reduces the chain separation required for penetrant motion transverse to the local chain axis. The theory is then identical to that of Part I, except that penetrant diameters minus a constant factor are employed in place of the normal diameters. In most of the cases studied the reduction factor for a given polymer may be estimated with reasonable precision from chain geometry data. This diameter-reduction effect is the likely explanation of the apparent proportionality between the activation energy of diffusion and the square of the penetrant diameter reported earlier for vinyl polymers. The data quoted here and in Part II are analyzed to give a semitheoretical correlation between the effective jump length L? and ΔE, the activation energy of diffusion. This correlation appears to be equally valid for glassy and rubbery noncrystalline polymers.     

Microchemical urinalysis: IX. Determination of hydroxyproline in urine

A simplified procedure is described for the determination of hydroxyproline in human or monkey urine. In this procedure I ml of urine is subjected in succession to hydrolysis, oxidation, extraction and color development. During these steps impurities and interfering substances are eliminated, thus resulting in a chromophore due to hydroxyproline alone. Thirty-five urine samples can be analyzed in one working day.     

Model of sorption of simple molecules in polymers

A model of simple molecule sorption in polymers is proposed which embraces both the glassy and rubbery regions, and incorporates the successful dual-mode model below the glass-transition temperature. Hole filling is shown to be an important sorption mechanism both above and below T_g, although saturation effects do not occur in the rubbery polymer. The model interprets the “dual-mode” Langmuir and Henry's law parameters at the molecular level, and a simple statistical mechanical analysis allows estimation of the parameter values, as well as specifying certain interrelationships between the parameters. Applications of the model to gas solubility data in five polymers are considered [polyethylene (PE), poly(ethylene terephthalate) (PET), polystyrene (PS), polymethacrylate (PMA), poly(vinyl acetate) (PVAc)] and semiquantitative agreement is obtained for PE, PET, and to a lesser extent, PS. For PMA and PVAc, the agreement is qualitative only.     

Self-amplified spontaneous emission free-electron laser with an energy-chirped electron beam and undulator tapering

We report the first experimental implementation of a method based on simultaneous use of an energy chirp in the electron beam and a tapered undulator, for the generation of ultrashort pulses in a self-amplified spontaneous emission mode free-electron laser (SASE FEL). The experiment, performed at the SPARC FEL test facility, demonstrates the possibility of compensating the nominally detrimental effect of the chirp by a proper taper of the undulator gaps. An increase of more than 1 order of magnitude in the pulse energy is observed in comparison to the untapered case, accompanied by FEL spectra where the typical SASE spiking is suppressed.