Wania Wolff

Absolute total and partial dissociative cross sections of pyrimidine at electron and proton intermediate impact velocities.

Absolute total non-dissociative and partial dissociative cross sections of pyrimidine were measured for electron impact energies ranging from 70 to 400 eV and for proton impact energies from 125 up to 2500 keV. MOs ionization induced by coulomb interaction were studied by measuring both ionization and partial dissociative cross sections through time of flight mass spectrometry and by obtaining the branching ratios for fragment formation via a model calculation based on the Born approximation. The partial yields and the absolute cross sections measured as a function of the energy combined with the model calculation proved to be a useful tool to determine the vacancy population of the valence MOs from which several sets of fragment ions are produced. It was also a key point to distinguish the dissociation regimes induced by both particles. A comparison with previous experimental results is also presented.

Electron-recoil ion and recoil ion-projectile coincidence techniques applied to obtain absolute partial collision cross sections

We present in detail an alternative experimental set-up and data analysis, based on the electron-recoil ion and recoil ion-projectile coincidence techniques, that enable the measurement of partial pure ionization and partial charge exchange cross sections for an effusive gas jet set-up, where the absolute target density and recoil ion efficiency cannot be measured directly. The method is applied to the ionization of helium atoms due to collision with partially stripped C(3 +) projectiles. In order to check the method, the results are compared to data available in the literature where the target density and recoil ion detection efficiency were measured directly. The pure ionization channel is compared to the electron capture channel.

Source of slow lithium atoms from Ne or H2 matrix isolation sublimation.

We have studied, via laser absorption spectroscopy, the velocity distribution of (7)Li atoms released from cryogenic matrices of solid neon or molecular hydrogen. The Li atoms are implanted into the Ne or H(2) matrices--grown onto a sapphire substrate--by laser ablation of a solid Li or LiH precursor. A heat pulse is then applied to the sapphire substrate sublimating the matrix together with the isolated atoms. With a NiCr film resistor deposited directly onto the sapphire substrate we are able to transfer high instantaneous power to the matrix, thus reaching a fast sublimation regime. In this regime the Li atoms can get entrained in the released matrix gas, and we were also able to achieve matrix sublimation times down to 10 μs for both H(2) or Ne matrix, enabling us to proceed with the trapping of the species of our interest such as atomic hydrogen, lithium, and molecules. The sublimation of the H(2) matrix, with its large center-of-mass velocity, provides evidence for a new regime of one-dimensional thermalization. The laser ablated Li seems to penetrate the H(2) matrix deeper than it does in Ne.

Doubly and Triply Charged Species Formed from Chlorobenzene Reveal Unusual C–Cl Multiple Bonding

In free-radical halogenation of aromatics, singly charged ions are usually formed as intermediates. These stable species can be easily observed by time-of-flight mass spectrometry (TOF-MS). Here we used electron and proton beams to ionize chlorobenzene (C6H5Cl) and investigate the ions stability by TOF-MS. Additionally to the singly charged parent ion and its fragments, we find a significant yield of doubly and triply charged parent ions not previously reported. In order to characterize these species, we used high-level theoretical methods based on density functional theory (DFT), coupled-cluster (CC), and generalized valence bond (GVB) to calculate the structure, relative stabilities, and bonding of these dications and trications. The most stable isomers exhibit unusual carbon-chlorine multiple bonding: a terminal C═Cl double bond in a formyl-like CHCl moiety (1, rC-Cl = 1.621 Å) and a ketene-like C═C═Cl cumulated species (2, rC-Cl = 1.542 Å). The calculations suggest that an excited state of 2 has a nitrile-like C≡Cl triple bond structure.

SINGLE AND DOUBLE PHOTOIONIZATION AND PHOTODISSOCIATION OF TOLUENE BY SOFT X-RAYS IN A CIRCUMSTELLAR ENVIRONMENT

The formation of polycyclic aromatic hydrocarbons (PAHs) and their methyl derivatives occurs mainly in the dust shells of asymptotic giant branch (AGB) stars. The bands at 3.3 and 3.4

Slow ground state molecules from matrix isolation sublimation

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A small multiparameter data acquisition system for nuclear spectroscopy

m, observed in infrared emission spectra of several objects, are attributed C-H vibrational modes in aromatic and aliphatic structures, respectively. In general, the feature at 3.3

Heteronuclear molecules from matrix isolation sublimation and atomic diffusion

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Methyl formate ice stimulated by X-rays in protoplanetary discs

m is more intense than the 3.4

Non-thermal desorption processes on nitrile-bearing astrophysical ice analogues studied by electron stimulated ion desorption

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