Passive mode locking of a Nd:YVO4 laser with an extra-long optical resonator

We describe a mode-locked, diode-pumped Nd:YVO4 laser with a very long optical cavity operating at 1064 nm. High-modulation, InGaAs quantum-well, semiconductor saturable-absorber mirrors were used for passive mode locking, providing a stable train of 13-ps pulses. A novel zero-q-transformation multipass cell provided a variable-length optical cavity as much as 100 m long. The output beam had M2 < 1.1 at average powers of 4.1, 3.9, and 3.5 W at repetition rates of 4.1, 2.6, and 1.5 MHz, respectively. To the best of our knowledge the last of these is the lowest repetition rate ever generated directly from a mode-locked nonfiber solid-state laser without cavity dumping.     

Structure and ultrafast dynamics of liquid water: a quantum mechanics/molecular mechanics molecular dynamics simulations study

A quantum mechanics/molecular mechanics molecular dynamics simulation was performed for liquid water to investigate structural and dynamical properties of this peculiar liquid. The most important region containing a central reference molecule and all nearest surrounding molecules (first coordination shell) was treated by Hartree-Fock (HF), post-Hartree-Fock [second-order Moller-Plesset perturbation theory (MP2)], and hybrid density functional B3LYP [Becke's three parameter functional (B3) with the correlation functional of Lee, Yang, and Parr (LYP)] methods. In addition, another HF-level simulation (2HF) included the full second coordination shell. Site to site interactions between oxygen-oxygen, oxygen-hydrogen, and hydrogen-hydrogen atoms of all ab initio methods were compared to experimental data. The absence of a second peak and the appearance of a shoulder instead in the gO-O graph obtained from the 2HF simulation is notable, as this feature has been observed so far only for pressurized or heated water. Dynamical data show that the 2HF procedure compensates some of the deficiency of the HF one-shell simulation, reducing the difference between correlated (MP2) and HF results. B3LYP apparently leads to too rigid structures and thus to an artificial slow down of the dynamics.     

Komplexe von Acetylaceton und Acetonylaceton mit Alkali- und Erdalkaliionen. MO-SCF-Berechnungen und UV-Spektroskopie

In analogy to previous investigations on main group metal ion complexes with diacetyl², model calculations within the LCGO MO SCF framework using minimal basis sets are used in combination with UV spectrocopy in order to investigate complex formation tendencies, eventual ion specifities and ion binding energies of Li, Na, K, Mg and Ca ions with dicarbonyl ligands. The influence of the separation of the coordinative centers by methylene groups on the interaction with these metal ions is discussed. The simple quantum chemical models seem to work in the case of diacetyl and acetylacetone, whereas they fail in the prediction of the experimentally observed interaction of acetonylacetone with the metal ions.

     

Amplifier module of the “Del'fin” facility for thermonuclear plasma heating

The construction principle and the applicable system are considered for the highpower laser amplifier module of the “Del'fin” facility, intended for spherical heating of thermonuclear targets. Results are presented of investigations of the radiation parameters of the amplifier module under various operating regimes. The system for focusing the laser radiation on the target surfaces is described and the results of experiments on plasma heating by radiation of three composite laser beams, at a laser energy level up to 1 kJ at a flux density up to 10¹⁴ W/cm², are analyzed.     

Dynamics of light-induced reflectivity switching in gallium films deposited on silica by pulsed laser ablation

We present what is to our knowledge the first experimental study of light-induced reflectivity changes at an alpha-Ga/Si interface irradiated by femtosecond and picosecond laser pulses. After exposure, the reflectivity can increase from R?0.55 , which is typical for alpha-Ga , to R?0.8 , which is close to that of liquid Ga. The initial step in the reflectivity change of 2-4 ps is resolved with 150-fs laser pulses. The light-induced reflectivity change relaxes during 100ns-10 mus , depending strongly on the background temperature of the Ga mirror and the laser fluence.     

On water direct arylation of imidazo[1,2-a]pyridines with aryl halides

A simple, mild, and ecofriendly protocol for a palladium-catalysed direct arylation of imidazo[1,2-a]pyridines with aryl halides on water is reported. This protocol does not require any ligand and tolerate variety of functional groups on both the coupling partners. The simple base KOH is highly efficient in this transformation.

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Temperature dependence of structure and dynamics of the hydrated Ca2+ ion according to ab initio quantum mechanical charge field and classical molecular dynamics

Simulations using ab initio quantum mechanical charge field molecular dynamics (QMCF MD) and classical molecular dynamics using two‐body and three‐body potentials were performed to investigate the hydration of the Ca²⁺ ion at different temperatures. Results from the simulations demonstrate significant effects of temperature on solution dynamics and the corresponding composition and structure of hydrated Ca²⁺. Substantial increase in ligand exchange events was observed in going from 273.15 K to 368.15 K, resulting in a redistribution of coordination numbers to lower values. The effect of temperature is also visible in a red‐shift of the ion‐oxygen stretching frequencies, reflecting weakened ligand binding. Even the moderate increase from ambient to body temperature leads to significant changes in the properties of Ca²⁺ in aqueous environment. © 2009 Wiley Periodicals, Inc. J Comput Chem, 2010     

High precision delta(17)O isotope measurements of oxygen from silicates and other oxides: method and applications

The use of infrared laser-assisted fluorination to release oxygen from milligram quantities of silicates or other oxide mineral grains is a well-established technique. However, relatively few studies have reported the optimisation of this procedure for oxygen-17 isotope measurements. We describe here details of an analytical system using infrared (10 μm) laser-assisted fluorination, in conjunction with a dual inlet mass spectrometer of high resolving power ( approximately 250) to provide (17)O and (18)O oxygen isotope measurements from 0.5-2 mg of silicates or other oxide mineral grains. Respective precisions (1) of typically 0.08 and 0.04 per thousand are obtained for the complete analytical procedure. Departures from the mass-dependent oxygen isotope fractionation line are quantified by Delta(17)O; our precision (1) of such measurements on individual samples is shown to be +/-0.024 per thousand. In turn, this permits the offset between parallel, mass-dependent fractionation lines to be characterised to substantially greater precision than has been possible hitherto. Application of this system to investigate the (17)O versus (18)O relationship for numerous terrestrial whole-rock and mineral samples, of diverse geological origins and age, indicates that the complete data set may be described by a single, mass-dependent fractionation line of slope 0.5244+/- 0.00038 (standard error). Copyright 1999 John Wiley & Sons, Ltd.