Modification of multiphoton ionization spectra via third harmonic generation in focused laser beams

The modification of multiphoton ionization spectra through third harmonic generation in focused laser beam geometries is reported. A strong enhancement of the ionization peaks corresponding to the decay of thenf' autoionizing series of Kr and the observation of a double resonance in Xe, which is missing in low atomic density spectra, is shown to originate from excitation channels involving absorption of third harmonic photons. This excitation is demonstrated to occur in a significantly extended volume outside the focal region, thus strongly increasing the ionization yield.     

Experimental and Computational Study of the Thermal Decomposition of 3‐Methyl‐3‐buten‐1‐ol in m‐Xylene Solution

An experimental study of the thermal decomposition of a β‐hydroxy alkene, 3‐methyl‐3‐buten‐1‐ol, in m‐xylene solution, has been carried out at five different temperatures in the range of 513.15–563.15 K. The temperature dependence of the rate constants for the decomposition of this compound in the corresponding Arrhenius equation is given by ln k (s^?1) = (25.65 ± 1.52) ? (17,944 ± 814) (kJ·mol^?1)·T^?1. A computational study has been carried out at the M05–2X/6–31+G(d,p) level of theory to calculate the rate constants and the activation parameters by the classical transition state theory. There is a good agreement between the experimental and calculated rate constants and activation Gibbs energies. The bonding characteristics of reactant, transition state, and products have been investigated by the natural bond orbital analysis, which provides the natural atomic charges and the Wiberg bond indices. Based on the results obtained, the mechanism proposed is a one‐step process proceeding through a six‐membered cyclic transition state, being a concerted and slightly asynchronous process. The results have been compared with those obtained previously by us (Struct Chem 2013, 24, 1811–1816) for the thermal decomposition of 3‐buten‐1‐ol, in m‐xylene solution. We can conclude that in the compound studied in this work, 3‐methyl‐3‐buten‐1‐ol, the effect of substitution at position 3 by a weakly activating CH₃ group is the stabilization of the transition state formed in the reaction and therefore a small increase in the rate of thermal decomposition.     

Structural and Kinetic Aspects of Blood Plasma Protein Adsorption on the Surface of Hydrophobic Polymers

Abstract

Due to the wide use of polymers in medicine, researchers are required to solve a very important problem–to understand the interaction between materials of nonphysiological origin and the surrounding biological liquids, and tissues, particularly blood.     

BLUE AND GREEN LIGHT EFFECTS,AND THEIR PHOTOREVERSIBILITY,UPON ZOOSPORE PRODUCTION AND THE SYNCHRONIZED CYCLE IN PROTOSIPHON BOTRYOIDES KLEBS*

Abstract —The synchronized asexual cycle in Protosiphon botryoides Klebs is described. A blue light (430 nm) inhibition of zoospore production can be photoreversed by green light (550 nm). Similarly, a green light (550 nm) stimulation of zoospore production can be photoreversed by blue (430 nm) light. 430 nm light also shortens the period of zoospore motility, and 550 nm light lengthens this period.     

Nucleon structure functions from high energy neutrino interactions

Structure functions obtained from high energy neutrino and antineutrino scattering from an iron target are presented. These were extracted from the combined data of Fermilab experiments E616 and E701; these utilized narrow band beam runs between 1979–1982. The structure functions are used to test the validity of quarkparton model (QPM) predictions and to extract the QCD scale parameter Λ from fits to the Altarelli-Parisi equations.