Gas Phase Formation of Methylgermylene (HGeCH3)

The methylgermylene species (HGeCH₃; X¹A′) has been synthesized via the bimolecular gas phase reaction of ground state methylidyne radicals (CH) with germane (GeH₄) under single collision conditions in crossed molecular beams experiments. Augmented by electronic structure calculations, this elementary reaction was found to proceed through barrierless insertion of the methylidyne radical in one of the four germanium-hydrogen bonds on the doublet potential energy surface yielding the germylmethyl (CH₂GeH₃; X²A′) collision complex. This insertion is followed by a hydrogen shift from germanium to carbon and unimolecular decomposition of the methylgermyl (GeH₂CH₃; X²A′) intermediate by atomic hydrogen elimination leading to singlet methylgermylene (HGeCH₃; X¹A′). Our investigation provides a glimpse at the largely unknown reaction dynamics and isomerization processes of the carbon-germanium system, which are quite distinct from those of the isovalent carbon system thus providing insights into the intriguing chemical bonding of organo germanium species on the most fundamental, microscopic level.     

Physical processes during development of upward leaders from tall structures

The objective of our study was to identify and interpret the various processes during development of upward positive leaders from tall structures. We provide a physical interpretation for the varying luminosity of the leader channel during its initial ascent and the pulsing luminosity during much later stages of the established leader. Our analysis confirms that pulsed luminosity is a result of recoil leaders intercepting the current-carrying channel connected to ground. This interception produces an M-component. Applying the bidirectional leader concept and a simplified electrostatic approximation, we introduce physical models of the dart leader-return stroke sequence and the M-component.     

Particle tunneling and scattering in a three-dimensional potential with a barrier

The particle tunneling through a 3-D rectangular potential barrier has been studied. The simplest model for multiple internal reflections has been assumed. The explicit expression for all the transmission and reflection probability amplitudes have been derived, as well as the tunneling and reflection phase times.      

A rapid method of synthesizing the layered titanosilicate JDF-L1

A rapid procedure for synthesis of highly crystalline and pure samples of JDF-L1 without using organics are reactants or templates is described and indexation of the powder X-ray diffraction pattern of this phase is presented.     

Use of electron correlation to make attosecond measurements without attosecond pulses

We describe how correlations between electrons can be used to trace the dynamics of correlated two-electron ionization with attosecond precision, without using attosecond pulses. The approach is illustrated using the example of Auger or Coster-Kronig decay triggered by photoionization with an extreme ultraviolet pulse. It requires correlated measurements of angle-resolved energy spectra of both the photo- and Auger electrons in the presence of a laser pulse. To reconstruct the dynamics, we use not only classical time and energy correlation, but also entanglement between the two electrons.