ABSTRACT
IR spectra in the 'Finger Print' spectral range has great importance in qualitative and quantitative analysis of explosives like trinitrotoluene (TNT) and cyclotrimethyltrinitramine (RDX). Highly resolved IR bands of these compounds have been recorded in the 9.6 and 10.6 microm regions of CO2 laser. TNT and RDX are large molecules each having 21 atoms and it is very difficult to assign the modes of vibrations by comparison with those in other molecules making the vibrational assignments of observed bands a difficult task. The ab initio quantum chemical calculation is used for determining the molecular geometries and modes of vibration of these molecules with a view to assign their normal modes in the high resolution vibrational photoacoustic spectra. These assignments are very reliable in view of the good agreement between the observed and calculated frequencies of deuterated TNT.
Subject(s)
Carbon Dioxide/chemistry , Lasers , Triazines/chemistry , Trinitrotoluene/chemistry , Spectrophotometry, InfraredABSTRACT
In Ref. 1, the first full sentence in the right-hand column of p. 1608 should read as: 'Although BBO is phase matchable down to 187 nm and shorter in this configuration without a very large (2-4 degrees ) change in theta (and hence in d(eff)), and B2 is also suitable to accommodate the phase matching, tunability below 187.9 nm becomes limited by the exponential increase in crystal absorption.'
ABSTRACT
Tunable ultraviolet radiation in the 200-230-nm region has been generated with beta barium borate crystals by type I sum-frequency mixing of the second harmonic with the fundamental beam from a dye laser pumped by the second harmonic of the same Nd:YAG laser. A noncollinear phase-matching configuration has made it possible to realize conversion efficiency of 21% at 208.3 nm with input power densities as low as 28 MW/cm(2) for the fundamental and 2.4 MW/cm(2) for its second-harmonic radiation. The absorption characteristic of a standard DNA sample has been studied with the generated tunable ultraviolet source, revealing additional features compared with those obtained with a spectrophotometer.
ABSTRACT
Tunable 187.9-196-nm vacuum-ultraviolet radiation was generated at room temperature in a beta barium borate crystal by sum-frequency mixing of Nd:YAG laser radiation and the second harmonic of a dye laser pumped by the second harmonic of the same Nd:YAG laser. By use of the advantageous noncollinear phase-matching configuration, a peak power of 1.3 kW was obtained at 194 nm with input power densities as low as 79MW/cm(2) for 1064-nm and 0.65MW/cm(2) for 237.3-nm radiation.
ABSTRACT
Efficient generation of mid-infrared radiation by noncritically phase-matched second-harmonic generation is demonstrated in a mixed chalcopyrite crystal, AgGa(x)In(1-x)Se(2), and compared with that in an AgGaSe(2) crystal. Nonlinear coeff icients d(36) of AgGa(x)In(1-x)Se(2) and AgGaSe(2) crystals have also been derived.
ABSTRACT
Refractive indices of AgGaS2 crystal are measured at different temperatures using the classical minimum deviation technique and are fitted in appropriate dispersion relations. The variation of pump laser wavelength for noncritical upconversion of signal at 10.6 microm with the change in crystal temperature has been verified using the above data. Temperature tunable infrared generation by noncritically phase-matched difference- frequency mixing has been predicted from 3 to 18 microm.