﻿<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>Laser Chemistry</title><link>http://www.hindawi.com</link><description>The latest articles from Hindawi Publishing Corporation</description><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright><item><title>Laser-Induced Backside Wet Etching of Transparent Materials with Organic and Metallic Absorbers</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/170632</link><description>Laser-induced backside wet etching (LIBWE) allows the high-quality etching of transparent materials for micro- and nanopatterning. Recent own results of LIBWE with hydrocarbon and metallic absorbers (H- and M-LIBWE) are summarized and compared with selected results of other groups regarding the etching process and the etched surface. Significant results on the impact of the liquid absorber, the material and the wavelength, and the pulse length of the laser to the etching are selected for this comparison. The etching of submicron-sized periodic structures in sapphire and fused silica with interference techniques and the selection of the preferred method in dependence on the material and the processing goal  discussed. The experimental results are discussed on a thermal model considering both interface and volume absorption of the laser beam. These results have the conclusion that the etching at M-LIBWE is mainly due to material melting and evaporation whereas at H-LIBWE, a modified near-surface region with a very high absorption is ablated.</description><Author>K. Zimmer and R. B&amp;#246;hme</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Three-Dimensional Modeling of the Heat-Affected Zone in Laser Machining Applications</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/976205</link><description>Thermal load as well as its three-dimensional (3D) spatial distribution
has been estimated inside representative materials: glass (low thermal
diffusion), silicon (semimetal properties), and sapphire (a crystalline dielectric
of a high thermal conductivity) for typical laser processing and
direct laser writing applications. The 3D temperature distribution allows
to calculate thermal stress around the focal region. This provides an
assessment tool for optimization of laser microprocessing conditions for
controlled laser dicing and cutting applications.</description><Author>Martynas Beresna, Titas Gertus, Rolandas Toma&amp;#353;i&amp;#363;nas, Hiroaki Misawa, and Saulius Juodkazis</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Two-Photon Polymerization of Hybrid Sol-Gel Materials for Photonics Applications</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/493059</link><description>Two-photon polymerization of photosensitive materials has emerged as a very promising technique for the fabrication of photonic crystals and devices. We present our investigations into the structuring by two-photon polymerization of a new class of photosensitive sol-gel composites exhibiting ultra-low shrinkage. We particularly focus on two composites, the first containing a zirconium alkoxide and the second a nonlinear optical chromophore. The three-dimensional photonic crystal structures fabricated using these materials demonstrate high resolution and clear bandstops in the near IR region.</description><Author>A. Ovsianikov, A. Gaidukeviciute, B. N. Chichkov, M. Oubaha, B. D. MacCraith, I. Sakellari, A. Giakoumaki, D. Gray, M. Vamvakaki, M. Farsari, and C. Fotakis</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Processing of Dielectric Optical Coatings by Nanosecond and Femtosecond UV Laser Ablation</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/623872</link><description>Microprocessing of dielectric optical coatings by UV laser ablation is demonstrated. Excimer laser ablation at deep UV wavelengths (248&amp;#x2009;nm, 193&amp;#x2009;nm) is used for the patterning of thin oxide films or layer stacks. The layer removal over extended areas as well as sub-&amp;#x03BC;m-structuring is possible. The ablation of SiO2, Al2O3, HfO2, and Ta2O5 layers and layer systems has been investigated. Due to their optical, chemical, and thermal stability, these inorganic film materials are well suited for optical applications, even if UV-transparency is required. Transparent patterned films of SiO2 are produced by patterning a UV-absorbing precursor SiOx suboxide layer and oxidizing it afterwards to SiO2. In contrast to laser ablation of bulk material, in the case of thin films, the layer-layer or layer-substrate boundaries act as predetermined end points, so that precise depth control and a very smooth surface can be achieved. For large area ablation, nanosecond lasers are well suited; for patterning with submicron resolution, femtosecond excimer lasers are applied. Thus the fabrication of optical elements like dielectric masks, pixelated diffractive elements, and gratings can be accomplished.</description><Author>J. Ihlemann, J. B&amp;#233;k&amp;#233;si, J.-H. Klein-Wiele, and P. Simon</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Three-Dimensional Residue-Free Volume Removal inside Sapphire by High-Temperature Etching after Irradiation of Femtosecond Laser Pulses</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/892721</link><description>We applied the femtosecond laser-assisted etching technique, that is, irradiation of focused femtosecond
laser pulses followed by selective chemical etching, to volume removal inside sapphire.
At room temperature, volume etching only slightly advanced while residue remained inside the
volume. By increasing the etching temperature, complete volume etching without residue was
achieved. Complete etching was, however, accompanied by undesirable phenomena of surface pits
or cracks, which are expected to be excluded through further improvement of processing.</description><Author>Shigeki Matsuo, Kensuke Tokumi, Takuro Tomita, and Shuichi Hashimoto</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Physical and Spectroscopic Properties of Yb3+-Doped Fluorophosphate Laser Glasses</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/656490</link><description>The physical properties including refractive index, Abbe number, nonlinear refractive index, microhardness and thermal expansion coefficient, and spectroscopic properties of Yb3+-doped fluorophosphate laser glasses were investigated. The results show that due to the addition of fluoride, mechanical and thermal properties are promoted, emission cross-section &amp;#x03C3;emi is also greatly enhanced. The largest gain coefficient &amp;#x03C3;emi&amp;#x00B7;&amp;#x03C4;m (0.824&amp;#x2009;pm2&amp;#x00B7;ms) can be obtained with the minimum pump intensity Imin (1.112&amp;#x2009;kw/cm2). This kind of Yb3+-doped fluorophosphate glass is an excellent candidate material for Yb3+-doped host for high-power generation.</description><Author>Shujiang Liu and Anxian Lu</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Ultrafast Four-Wave Optical Parametric Amplification in Transparent Condensed Bulk Media</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/534951</link><description>We present a short overview of recent advances in ultrashort pulse four-wave optical parametric
amplification in transparent condensed bulk media with Kerr nonlinearity. Highly efficient (10&amp;#37; to 15&amp;#37; pump-to-signal energy conversion) four-wave optical parametric amplification in water and fused silica is experimentally demonstrated. The amplification process highly benefits from 1-dimensional spatial soliton propagation regime, which sets in under proper combination of cylindrical beam focusing and noncollinear phase matching geometry with millijoule pumping. Under these operating conditions, strong four-wave coupling quenches catastrophic beam break-up and filamentation, and the setup operates reasonably below the damage threshold of the nonlinear medium. The proposed methodology offers a number of advantages as compared to guided-wave configurations in gaseous media.</description><Author>Audrius Dubietis, Gintaras Tamo&amp;#353;auskas, Gintaras Valiulis, and Algis Piskarskas</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Induced Bragg Gratings in Optical Fibers and Waveguides Using an Ultrafast Infrared Laser and a Phase Mask</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2008/416251</link><description>Since its development in 2003, the technique of Bragg grating inscription in optical fibers and waveguides with ultrafast infrared radiation and a phase mask has proven to be as simple as the standard UV-laser grating writing techniques but far more versatile. The ultrafast IR laser-based process allows for the creation of grating structures in glassy and crystalline materials that are not typically UV photosensitive.  In this article, we will review the studies that have been performed at the Communications Research Centre Canada on the grating formation processes as well as applications of the ultrafast laser technique to fabricate gratings in various optical fibers and waveguides.</description><Author>Stephen J. Mihailov, Dan Grobnic, Christopher W. Smelser, Ping Lu, Robert B. Walker, and Huimin Ding</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Cellular Damage in Diabetic Wounded Fibroblast Cells following Phototherapy at 632.8, 830, and 1064 nm</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2007/80536</link><description>Objective. This study aimed to establish if laser irradiation induces cellular and genetic damage. Background.  Phototherapy has been shown to induce wound healing in diabetic wounds, however little information is known regarding light-induced damage. Methods. Diabetic wounded fibroblasts were irradiated with 5 or 16&amp;#x2009;J/cm2 at 632.8, 830, and 1064&amp;#x2009;nm. Damage was assessed by measuring membrane and DNA damages. Cellular migration was determined by microscopy. Results. Cells irradiated with 5&amp;#x2009;J/cm2 at 632.8 and 830&amp;#x2009;nm showed a significant decrease in DNA damage while all cells irradiated with a fluence of 16&amp;#x2009;J/cm2 showed an increase in membrane and DNA damages. Conclusion. This study showed that the comet assay and LDH release were sensitive enough to pick up changes in laser-irradiated cells. This study also showed that cellular and genetic damage inflicted on diabetic wounded cells was dependent on dose and wavelength and that cells are able to recover and respond.</description><Author>Nicolette N. Houreld and Heidi Abrahamse</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Near-Resonant Nonlinear Optical
Properties of Pseudoisocyanine J-Aggregates in Langmuir-Blodgett
Layers</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1997/95890</link><description>The nonlinear optical properties of pseudoisocyanine J-aggregates in Langmuir-Blodgett
films have been investigated by means of degenerate four wave mixing (DFWM) process.
The conversion efficiency of the DFWM signal and the estimated third order
susceptibility were found to be comparable with those of pseudoisocyanine J-aggregates
in solution under comparable resonance conditions. The intensity dependence of the
converted (DFWM) signal is interpreted as resulting from different processes including
saturation, exciton-exciton annihilation and secondary processes of dynamical disorder.</description><Author>K.-H. Feller, R. Gadonas, A. Pugzlys, and D. M&amp;#246;bius</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Photofragmentation of Cl2 at 308 nm</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/31690</link><description>The velocity distributions for the Cl(2P3/2) and Cl(2P1/2) photofragments produced by the
photolysis of Cl2 at 308 nm are measured using ion imaging. The angular distributions
yield anisotropy parameters of &amp;#x03B2;(2P3/2)=&amp;#x2212;1.00&amp;#x00B1;0.05,&amp;#x03B2;(2P1/2)=&amp;#x2212;0.95&amp;#x00B1;0.05, suggesting
that Cl(2P3/2) and Cl(2P1/2) is essentially produced via non-adiabatic curve crossing between
the lu and the 0u+ excited electronic states.</description><Author>Peter C. Samartzis, Theodosia Gougousi, and Theofanis N. Kitsopoulos</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Single Pulse Carbon-13 Enrichment of CF3 Under IR MPD in A Short
Gas Dynamic Flow</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/36263</link><description>An experimental approach is described for obtaining highly enriched residual gas under
IR multiphoton dissociation (MPD) of molecules in one cycle of irradiation. The
approach is based on utilization of a pulsed molecular flow of small length (&amp;#x0394;xfl&amp;#x2264;1cm).
The use of a short flow length leads to high values of the dissociation yield of molecules
(&amp;#x03B2;&amp;#x2243;1) in the whole volume of the flow. Owing to this, high enrichment of the residual
gas is achieved in one cycle of irradiation. The isotopically-selective dissociation of CF3I+
in the pulsed gasdynamic flow of a small length was studied. About 400-fold enrichment
of the 13C isotope in the residual gas was obtained following irradiation of a molecular
flow of CF3I of natural isotope composition by a single laser pulse. The selectivity of
dissociation was measured to be &amp;#x03B1;&amp;#x2265;10</description><Author>G. N. Makarov, D. E. Malinovsky, and D. D. Ogurok</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Hydrophobicity of Water at the Surface as Studied by laser-Induced
Fluorescence Microscopy</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/57838</link><description>A sensitive comparative fluorescence microscopic approach was developed and used to
study the water at the air-water interface region. An insoluble chromophore mesoc-&amp;#945;,&amp;#946;,&amp;#947;,&amp;#948;-tetraphenylporphine (TPP) was spread on the water. Its fluorescence spectrum
indicated that the spectrum of TPP on the water surface was similar to those measured in
nonpolar hydrocarbon solvents. Thus, the water at the surface was concluded to be
hydrophobic and less polar than the water in the bulk.</description><Author>Yao-qun Li, Shinya Sasaki, Takanori Inoue, and Teiichiro Ogawa</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Photodissociation of Ozone at 248 nm and Vacuum Ultraviolet
Laser-Induced Fluorescence Detection of O(1D)</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/78967</link><description>Ozone molecules, O3, were photodissociated in the presence of N2 at 248 nm (KrF laser)
to O(1D)+ O2(1&amp;#8710;). The O(1D) atoms were detected by generating vacuum ultraviolet
laser-induced fluorescence (VUV LIF) for the 3s1D0 -2p 1D transition at 115.2 nm. The
115.2 nm probe laser was generated by frequency tripling (&amp;#969; vuv=3&amp;#969;) of the 345.6 nm
PTP dye laser in a Xe gas cell.</description><Author>A. M. Sarwaruddin Chowdhury</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Kinetic Study of the Reaction of Rh(a4F9/2) with N2O, O2 and NO</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/82640</link><description>The gas phase reactivity of Rh(a4F9/2) with N2O, O2 and NO is reported. Removal rate
constants for the excited states of rhodium below 13,000cm-1 are also reported. The
reaction rate of Rh(a4F9/2) with N2O is relatively temperature insensitive. The rate
constants for the bimolecular reaction are described in Arrhenius form by
(1.3&amp;#x00B1;0.3)&amp;#x00D7;10&amp;#x2212;12exp&amp;#x2061;(&amp;#x2212;1.3&amp;#x00B1;0.8KJ/mol/RT)cm3s&amp;#x2212;1 The reaction rates of the a4F9/2
state with O2 and NO are pressure dependent. For O2, the limiting low-pressure thirdorder,
K0, and limiting high-pressure second-order, K&amp;#8734;, room temperature rate constants in
argon buffer are (6.6&amp;#x00B1;0.6)&amp;#x00D7;10&amp;#x2212;30cm6s&amp;#x2212;1 and (2.1&amp;#x00B1;0.2)&amp;#x00D7;10&amp;#x2212;11cm3s&amp;#x2212;1, respectively.
For NO, K2 and K&amp;#8734; are (1.3&amp;#x00B1;0.2&amp;#x00D7;10&amp;#x2212;30cm6s&amp;#x2212;1) and (2.1&amp;#x00B1;0.4)&amp;#x00D7;10&amp;#x2212;11cm3s&amp;#x2212;1,
respectively. The removal rates of the excited states are faster than the ground state by a
factor of 2 or more.</description><Author>Mark L. Campbell</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Laser Desorption Dynamics of Carbendazim on a Glass Surface</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2000/13792</link><description>A study on the desorption of carbendazim (methyl-2-benzimidazolecarbamate, mass &amp;#61; 191 amu) from a glass surface (Pyrex) has been carried out using an experimental set-up
based on laser desorption and laser post-ionization followed by time-of-flight mass
spectrometry. After optimization of the experimental conditions a resolution of ca. 850
was achieved at the mass of the pesticide (191 amu). All measured time-of-flight mass
spectra showed not only an excellent signal to noise ratio, but also the lack of significant
molecular fragmentation, except for a mass of 71 amu which was attributed to the lateral
chain of the carbendazim. Neutral time-of-flight yields were measured for several desorption
energies. Analysis of the corresponding velocity distributions suggests a thermal
mechanism dominating the laser-induced desorption. Finally the capability of the
present technique for analytical applications is also discussed. </description><Author>B. Besc&amp;#243;s, J. M. Orea, and A. Gonzl&amp;#225;ez Ure&amp;#241;a</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Determination of Branching Ratios in a Kinetic Investigation of the Atomic Resonance Fluorescence and Molecular Chemiluminescence, CaCl(A2&amp;#x03A0;1/2,3/2,&amp;#x2009;B2&amp;#x03A3;+&amp;#x2009;&amp;#x2192;X2&amp;#x03A3;+), Resulting From the Reaction of Ca[4s4p(3PJ)] With CH3Cl Following Pulsed Dye Laser Excitation of Atomic Calcium</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2000/51834</link><description>Measurements in the time-domain of molecular chemiluminescence from CaCl(A2&amp;#x03A0;1/2,&amp;#x2009;A2&amp;#x03A0;2/3,&amp;#x2009;B2&amp;#x03A3;+&amp;#x2009;&amp;#x2192;X2&amp;#x03A3;+)and atomic resonance fluorescence from Ca(43P1&amp;#x2192;&amp;#x2009;41S0) have
been made in order to determine electronic branching ratios to yield CaCl(A1/2,&amp;#x2009;A2/3,&amp;#x2009;B)
following the Cl-atom abstraction reaction of electronically excited calcium atoms,
Ca[4s4p(3PJ)]
, 1.888 eV above the 4s2(1S0) ground state, with CH3Cl. Ca[4s4p(3P1)] was
generated by the pulsed dye-laser excitation ofground state calcium atoms at &amp;#955; &amp;#61; 657.3 nm
21, {Ca[4s4p(n3P1)]&amp;#x2009;&amp;#x2190;Ca[4s2(1S0)]} at elevated temigeratures in the presence of CH3Cl and
excess helium buffer gas in a slow flow system, kinetically equivalent to a static system.
Atomic and molecular emissions were recorded following rapid Boltzmann equilibration
within the Ca(43P0,1.2) spin-orbit manifold, atomic emission being restricted to
the 3P1 state as the 3P0 and 3P2 states are long-lived, being so called &amp;#8216;reservoir states&amp;#8217;. Atomic fluorescence emission profiles at the resonance wavelength together with the molecular chemiluminescence emissions CaCl (A2&amp;#x03A0;1/2&amp;#x2192;X2&amp;#x03A3;+,&amp;#x2009;&amp;#x0394;&amp;#x03BD;=0,&amp;#x2009;&amp;#x03BB;=621nm),CaClA2&amp;#x03A0;3/2&amp;#x2192;X2&amp;#x03A3;+,&amp;#x2009;&amp;#x0394;&amp;#x03BD;=0,&amp;#x2009;&amp;#x03BB;=618nm and CaCl(B2&amp;#x03A3;+&amp;#x2192;X2&amp;#x03A3;+,&amp;#x2009;&amp;#x0394;&amp;#x03BD;=0,&amp;#x2009;&amp;#x2009;&amp;#x03BB;=593nm)
 were recorded. The atomic and molecular emissions demonstrated exponential
decays characterised by decay coefficients which were equal under identical chemical
conditions thus demonstrating the production of CaCl(A2&amp;#x03A0;1/2,3/2,&amp;#x2009;B2&amp;#x03A3;+) by direct
reaction of Ca(3pJ) with CH3Cl. The combination of the time-dependences of the atomic and molecular profiles as a function of the concentration of CH3Cl together with the integrated atomic and molecular intensities, placed on a common intensity scale by calibration of the optical system against a spectral radiometer, yielded branching ratios into the A2&amp;#x03A0;1/2, A2&amp;#x03A0;3/2 and B2&amp;#x03A3;+ states of CaCl. These were found to be as follows: A1/
(2.6&amp;#x00B1;1.1)2&amp;#x00D7;10&amp;#x2212;3; A2/3(1.9&amp;#x00B1;0.8)&amp;#x00D7;10&amp;#x2212;3 and B(3.6&amp;#x00B1;2.0)&amp;#x00D7;10&amp;#x2212;4. To the best of our
knowledge, these data represent the first measurements of electronic branching ratios of
calcium chlorides into specific molecular states for reactions of Ca(3pJ) determined in the time-domain. The results are compared with various related data for total branching ratios into electronic states studied in the single collision condition for this atomic state
with CH3Cl using molecular beams. These are also compared with branching ratios of
SrCl(A2&amp;#x03A0;1/2,&amp;#x2009;A2&amp;#x03A0;2/3,&amp;#x2009;B2&amp;#x03A3;+)
 following the reaction of Sr[5s5p(3pJ)]+ CH2Cl2 investigated following pulsed dye-laser excitation where the yields of SrCl(A1/2,&amp;#x2009;A3/2,&amp;#x2009;B)were of similar low magnitudes.</description><Author>D. Husain, J. Geng, F. Castano, and M. N. Sanchez Rayo</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Scanning-Fit Analysis of fs-Spectroscopic Data</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2000/56406</link><description>The scanning-fit method was developed for the global data analysis of pump-probe data.
This method is useful in cases when pulse durations are adjusted to be short compared
with nuclear dynamics and long compared with the dephasing timescales. Then multiexponential
functions can be used to describe the mono molecular relaxation processes
and the scanning-fit method increases the accuracy of the calculated time constants,
yields detailed information about their ranges of confidence and their dependency from
each other. In this paper we describe the method in detail and demonstrate its application
to simulated data. Additionally, we report about the results which were obtained
from scanning-fit analysis in case of the photoisomerization of pinacyanol and the light
induced processes in phycocyanobilin.</description><Author>Mark Bischoff, Gregor Stobrawa, and Sabine Rentsch</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Pressure Dependence of Degenerate Four-Wave Mixing in SO2: Effect of the Thermal
Gratings</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2000/94548</link><description>The degenerate four wave mixing (DFWM) spectrum of the A(1A2)&amp;#x2190;&amp;#x2009;X(1A1) and
B(1B1)&amp;#x2190;&amp;#x2009;X(1A1) transitions of SO2 in the 299.5&amp;#8211;305 nm region is presented. It has been
found that the DFWM signal intensities are proportional to the cube of laser intensity
and the square of SO2 pressure. The DFWM signal increases dramatically with the
pressure of N2 as a buffer gas. The enhancement of the DFWM signal can be mainly
attributed to the thermal grating contribution. </description><Author>Shiming Shi, Deying Chen, Qike Zheng, Maria Person, and Qizong Qin</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Synthesis, Characterization and Theoretical Investigation on the Optical Nonlinearity
of WS4Co(dppe)(DMF) Heterometallic Cluster Compound</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/2000/98130</link><description>A novel hetero-metallic binuclear cluster WS4Co(dppe)(DMF) has been synthesized and characterized. The crystal has a structure of monoclinic space group P21. Ab initio CPHF calculations are performed on the static first hyperpolarizabilities of the molecular building blocks of the cluster. The microscopic structural origin of nonlinear optical properties are discussed in-depth. The charge-transfer between tungsten ion and cobalt ion in a molecular building block critically contributes to the optical nonlinearity, while the joint effect of the ligands makes sufficient enhancements. The study is helpful to search for novel IR nonlinear optical materials among the transition metal cluster compounds.</description><Author>Kechen Wu, Ping Lin, Xintao Wu, and Ling Chen</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>High Resolution Spectroscopy With Molecular Beams and Tunable Lasers</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/17364</link><description>High resolution Doppler-free laser techniques are used in beam experiments to improve
the spectroscopic description of complex diatomic molecules. The case of TiO is
considered here for its implication in reaction dynamics studies and its interest in
Astrophysics. Two absorption bands in the visible have been analyzed:
B3&amp;#x03A0;&amp;#x2212;X3&amp;#x2009;&amp;#x0394;(1&amp;#x2212;0) and c1&amp;#x03A6;&amp;#x2212;a1&amp;#x2009;&amp;#x0394;(0&amp;#x2212;0). Owing to accurate wavenumber measurements,
it has been possible to extend the analysis to high rotational quantum numbers
and to carry out detailed spectroscopic calculations. They show that a careful revisiting
of the TiO electronic structure is necessary. </description><Author>R. Vetter, P. Luc, and C. Amiot</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Nanosecond Versus, Picosecond Molecular Multiphoton Fragmentation of Ketene
and Cyclohexane</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/25701</link><description>Multiphoton dissociation of ketene was studied at 290.5 nm after irradiation of the first
excited singlet state with two different laser pulsewidths of 4 ns and 10 ps. Analysis of the
photofragment fluorescence spectra in the two time domains sheds light on the
mechanisms that are responsible for the production of the observed CH(A2&amp;#x0394;), &amp;#x2009;(B2&amp;#x03A3;&amp;#x2212;)
and C2(d3&amp;#x03A0;g) photofragments. Multiphoton ionization of cyclohexane induced by a
visible laser at 581 nm and its second harmonic at 290.5 nm was measured in the above
mentioned pulse duration regimes. Study of the dependence of the total ionization signal
on pressure and laser energy helps to clarify the role played by the giant resonance of this
molecule at 84000 cm-1 in the photoionization process. </description><Author>M. Castillejo, M. Mart&amp;#237;n, and R. de Nalda</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Carbon Isotope Selective Separation From MPD of CF3Br With a TEA CO2 Laser</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/29272</link><description>Pure CF3Br and mixtures of this substance with monoatomic (He, Ar and Xe),
homonuclear diatomic (H2, D2, N2), polyatomic gases (CF4) and NO have been
irradiated with a TEA CO2 laser. Carbon-13 enrichment factor and carbon-13 selectivity
have been estimated from the mass spectrometric analysis of the undissociated CF3Br as
a function of excitation wavelength, fluence, temperature and pressure. The irradiating
wavelength is a crucial parameter to achieve enrichment. The nature of the added gas
also affects considerably selectivity. Best enrichment is achieved in mixtures with NO due
to its radical-like character.</description><Author>J. I. del Barrio, R. Fern&amp;#225;ndez C&amp;#233;zar, and F. M. G.- Tablas</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Channels of Product Formation and Excited Molecules Relaxation atMultiphoton Dissociation of Chlorodifluoromethane</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1993/98452</link><description>C2F4, molecules have been for the first time directly proved to be generated in the reaction ofvibrationally-excited molecules CF2HCl. The contribution of this reaction to CF2HCl multiphotondissociation (MPD) products formation was shown to become predominant at the initial CF2HCl pressuresabout ten Torr. Also fast relaxation of the highly excited molecules CF2HCl on the product moleculesC2F4 was discovered.</description><Author>V. A. Dimand, K. K. Maltzev, A. A. Nadeikin, A. I. Nikitin, A. M. Velichko, and A. V. Vnukov</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>The Role of Electric Fields and Ion Concentrations in the Formation and Stabilization of High-n
Rydberg States</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/63741</link><description>ZEro Kinetic Energy (ZEKE) spectroscopy relies on electrons produced through delayed
field ionization of the narrow band of high-n Rydberg states which exist just below the
ionization limit of each ionic eigenstate. Using the unique properties of these weakly
bound, stable, high-n Rydberg states (ZEKE states) below the ionization limit rather
than the unbound states above the limit, as in PES, leads to an improvement in
resolution of more than two orders of magnitude. Several different types of ZEKE
experiments, each designed to probe the formation and stability of these states, are
presented here. These experiments were performed with pulsed and static electric fields of
different magnitude and duration at different ion concentrations. The results indicate an
enhanced ZEKE state decay with increasing electric field strengths and an enhanced
formation and stabilization with increasing ion concentrations. A strong interplay
between field strength and ion concentration ZEKE state formation is demonstrated.
The strong influence of electric fields and ion concentrations on the physical properties
of the ZEKE state, above and below the classical ionization threshold, is also
demonstrated through late time (tens of microseconds) decay rate measurements. </description><Author>A. Held and E. W. Schlag</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Study of Agricultural Samples by Laser Desorption Coupled With Resonance-Enhanced Multiphoton
Ionization and Time-of-Flight Mass Spectrometry: Application to Carbendazim Analysis in Pepper</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/68314</link><description>A method for the analysis of carbendazim in peper has been developed using
Supercritical Fluid Extraction (SFE) for the sample preparation and the combination
of Laser Desorption (LD) with Resonance Enhanced Multi-Photon Ionization (REMPI)
coupled to Time-of-Flight Mass Spectrometry (TOF-MS) for the detection. The method
allows the analysis of carbendazim in pepper reducing the sample preparation step and
avoiding the matrix effects present in classical GC and HPLC techniques, as well as the
problems related to the labile properties of carbendazim. The detection limit obtained is
of the same order of magnitude as the generally employed HPLC technique, but with
higher sensitivity and easier sample preparation. </description><Author>B. Besc&amp;#243;s, J. M. Orea, C. Montero, A. Gonz&amp;#225;lez Ure&amp;#241;a, A. Valverde, and A. Aguilera</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Polymeric Matrices for Lasing Dyes: Recent Developments</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1998/71976</link><description>An overview of recent results obtained by our group on the development of polymeric
solid-state media incorporating either Rhodamine or Coumarin dyes is presented. The
effect on the laser performance of the rigidity and viscoelastic properties of the polymeric
matrix has been investigated. Lasing efficiencies similar to those found in ethanolic
solution, and improved photochemical stability, as compared with that obtained in
previous polymeric materials, were demonstrated for solid solutions of Rhodamine 6G
(Rh6G) in appropriate copolymer formulations of 2-hydroxyethyl methacrylate
(HEMA) and methyl methacrylate (MMA). Further improvements in photostability
were obtained when modified Rh6G molecules were copolymerized with HEMA and
MMA. When samples of this new highly homogeneous gain medium were placed in a
rotating system, where the laser medium was scanned in a continuous way, a stable laser
output with no sign of degradation after 500,000 shots was accomplished for transversal
pumping at 337 nm with 1.7 mJ pulses from a N2-laser at 2 Hz repetition rate. </description><Author>A. Costela, I. Garcia-Moreno, J. M. Figuera, F. Amat-Guerri, and R. Sastre</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Time-Resolved Quadrupole Mass Spectrometric Studies on Pulsed Laser Ablation of TiO2</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1999/39826</link><description>Pulsed laser ablation of TiO2 at 355 nm and 532 nm has been investigated using an angleand
time-resolved quadrupole mass spectrometric technique. The major ablated species include O (m/e &amp;#61; 16), O2 (m/e &amp;#61; 32), Ti (m/e &amp;#61; 48), TiO (m/e &amp;#61; 64) and TiO2 (m/e &amp;#61; 80). The time-of-flight (TOF) spectra of ablated species are measured for the ionic and neutral ablated species, and they can be fitted by a Maxwell &amp;#8211; Boltzmann (M &amp;#8211; B) distribution with a center-of-mass velocity. The measured angular distributions of the ionic species (O+ and Ti+) and the neutral species (O and Ti) can be fitted with cos&amp;#x2061;n&amp;#x03B8; and a&amp;#x2009;cos&amp;#x2061;&amp;#x03B8;&amp;#x2009;+&amp;#x2009;(1&amp;#x2212;a)cos&amp;#x2061;n&amp;#x03B8;, respectively. In addition, a continuous wave oxygen molecular beam is
introduced into the ablated plume, and the enhancement of the signal intensities of TiO
is observed. It implies that the ablated Ti atoms/ions species can react with ambient
oxygen molecules in the gas phase. In the meanwhile, the physicochemical mechanism of
pulsed laser ablation of TiO2 is discussed. </description><Author>Yongxin Tang, Zhenhui Han, and Qizong Qin</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Multiphoton Ionization and Fragmentation of CS2 Under Intense Short Pulse Laser Radiation</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1999/43598</link><description>The interaction of CS2 with intense short pulse laser radiation is studied, experimentally
using time-of-flight mass spectroscopy. Laser pulses of 0.5 and 5 psec at 248 and 496 nm
have been used in order to investigate the effect of the wavelength and the pulse duration
on the molecular ionization and fragmentation. As shown, for low enough intensities
the parent molecular ion is present as the most important peak in all cases. Increasing
the intensity results in extensive fragmentation, where the molecular parent ion remains
always the more intense mass peak at 496 nm while at 248 nm S+ dominates the mass
spectra. Finally, the production of multiply charged fragments is more efficient at the
longer wavelength used. </description><Author>E. Koudoumas, R. De Nalda, C. Fotakis, and S. Couris</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item><item><title>Analytical Studies of Polychromes by Time-Integrated Laser-Induced
Breakdown Spectroscopy</title><link>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/1999/48171</link><description>Time integrated Laser Induced Breakdown Spectroscopy was applied to the study of real
samples of polychromes. Two samples respectively from the Spanish Baroque and from
the XV century were analysed. The time integrated spectra showed negligible contribution
of continuum background emission. The spectra of the Baroque sample indicated the
presence of vermilion; this was confirmed by Near Infrared Fourier Transform Spectroscopy.
LIBS spectra of the XV century sample showed Ca, Al, Mg, Na and Pb lines and
the molecular emissions CN(B-X) and C2(d-a). Relative spectral intensities were measured
as a function of the number of laser pulses delivered on the same position of the sample.
The LIBS analysis was compared to an exhaustive analytical study.</description><Author>Margarita Martin, Marta Castillejo, Ricardo Torres, and Diego Silva</Author><copyright>&amp;#169; 2008, Hindawi Publishing Corporation. All rights reserved.</copyright></item></channel></rss>