A new, low temperature long-pass cell for mid-infrared to terahertz spectroscopy and synchrotron radiation use.

A new cell has been designed for accurate spectroscopic measurements in the 80-400 K temperature range with variable path lengths from 3 to more than 141 m. The spectral coverage at these temperatures ranges from the visible to less than 10 cm(-1), thanks to the use of diamond windows. The design of the cryostat and vacuum setups allows vibration-free operation.

Upper limits for undetected trace species in the stratosphere of Titan.

In this paper we describe the first quantitative search for several molecules in Titan's stratosphere in Cassini CIRS infrared spectra. These are: ammonia (NH3), methanol (CH3OH), formaldehyde (H2CO), and acetonitrile (CH3CN), all of which are predicted by photochemical models but only the last of which has been observed, and not in the infrared. We find non-detections in all cases, but derive upper limits on the abundances from low-noise observations at 25 degrees S and 75 degrees N.

New laboratory intercomparison of the ozone absorption coefficients in the mid-infrared (10 μm) and ultraviolet (300-350 nm) spectral regions.

Knowing the ozone absorption cross sections in the ultraviolet and infrared spectral range, with an accuracy of better than 1%, is of the utmost importance for atmospheric remote-sensing applications. For this reason, various ozone intensity intercomparisons and measurements have been published these last years. However, the corresponding results proved not to be consistent and thus have raised a controversial discussion in the community of atmospheric remote-sensing.

Optimized spectral microwindows for data analysis of the Michelson Interferometer for Passive Atmospheric Sounding on the Environmental Satellite.

For data analysis of the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) atmospheric limb emission spectroscopic experiment on Environmental Satellite microwindows, i.e., small spectral regions for data analysis, have been defined and optimized.

Optimized forward model and retrieval scheme for MIPAS near-real-time data processing.

An optimized code to perform the near-real-time retrieval of profiles of pressure, temperature, and volume mixing ratio (VMR) of five key species (O(3), H(2)O, HNO(3), CH(4), and N(2)O) from infrared limb spectra recorded by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) experiment on board the European Space Agency (ESA) Environmental Satellite ENVISAT-1 was developed as part of a ESA-supported study. The implementation uses the global fit approach on selected narrow spectral intervals (microwindows) to retrieve each profile in sequence. The trade-off between run time and accuracy of the retrieval was optimized from both the physical and the mathematical points of view, with optimizations in the program structure, in the radiative transfer model, and in the computation of the retrieval Jacobian.

Laboratory intercomparison of the ozone absorption coefficients in the mid-infrared (10 microm) and ultraviolet (300-350 nm) spectral regions.

For the measurement of atmospheric ozone concentrations, the mid-infrared and ultraviolet regions are both used by ground-, air-, or satellite-borne instruments. In this study we report the first laboratory intercomparison of the ozone absorption coefficients using simultaneous measurements in these spectral regions. The intercomparison shows good agreement (around 98.

High-Resolution Infrared, Microwave, and Submillimeter-Wave Study of FClO(2) in the nu(2), nu(3), nu(4), and nu(6) Excited States.

A high-resolution analysis of the {nu(2), nu(3)} and {nu(4), nu(6)} bands of the two isotopomers of chloryl fluoride F(35)ClO(2) and F(37)ClO(2) has been carried out for the first time using simultaneously infrared spectra recorded around 16&mgr;m and 26&mgr;m with a resolution of ca. 0.003 cm(-1) and microwave and submillimeter-wave transitions occurring within the vibrational states 2(1), 3(1), 4(1), and 6(1).

The v(1)+v(3) Bands of the (16)O(17)O(16)O and (16)O(16)O(17)O Isotopomers of Ozone.

Using 0.002 cm(-1) resolution Fourier transform absorption spectra of an (17)O enriched ozone sample, an extensive analysis of the v(1)+v(3) bands of the (16)O(17)O(16)O and (16)O(16)O(17)O isotopomers of ozone has been performed for the first time. The experimental rotational levels of the (101) vibrational states were satisfactorily reproduced using a Hamiltonian matrix that takes into account the observed rovibrational resonances.

Absolute Intensities of the nu(1) and nu(3) Bands of (16)O(3).

New experimental data on the nu(1) and nu(3) bands of (16)O(3) improving the value of absolute line intensities have been obtained. The intensities of 295 lines have been measured with an average accuracy between 2.5% and 3% and the rotational expansion of the transition moment operators for the nu(1) and nu(3) bands has been deduced.

New High-Resolution Analysis of the 3nu(3) and 2nu(1) + nu(3) Bands of Nitrogen Dioxide (NO(2)) by Fourier Transform Spectroscopy.

Using new high-resolution Fourier transform spectra recorded at the University of Denver in the 2-µm region, a new and more extended analysis of the 2nu(1) + nu(3) and 3nu(3) bands of nitrogen dioxide, located at 4179.9374 and 4754.2039 cm(-1), respectively, has been performed.

High-Order Resonances in the Water Molecule.

The water-vapor spectra in the near-infrared and visible region were reanalyzed with the purpose of finding experimental evidences of unusual high-order resonance between "dark" high-bending and "bright" stretch vibration states. About 70 transitions to the (050), (060), (070), (080), (160), (061), (170), (071), and, even (0 10 0) bending states, and their resonating partners were assigned in the spectra that gives the experimental energy levels lying near or above the potential energy barrier to linearity. The assignments were confirmed by combination differences and simultaneous observation of both perturbed and perturbing levels.

New High-Resolution Analysis of the nu(3) Band of the (15)N(16)O(2) Isotopomer of Nitrogen Dioxide by Fourier Transform Spectroscopy.

New high-resolution Fourier transform absorption spectra of an (15)N(16)O(2) isotopic sample of nitrogen dioxide were recorded at the University of Bremen in the 6.3-µm region. Starting from the results of a previous study [Y.

Absolute nu(2) Line Intensities of HOCl by Simultaneous Measurements in the Infrared with a Tunable Diode Laser and Far-Infrared Region Using a Fourier Transform Spectrometer.

We have measured absolute line intensities in the nu(2) fundamental band at 1238 cm(-1) of both isotopomers of hypochlorous acid, HOCl. To obtain the partial pressure of the species in the sample mixture, unavailable through direct measurement since HOCl exists only in equilibrium with H(2)O and Cl(2)O and may decay by secondary reactions, we relied on known absolute line intensities in the pure rotational far-infrared (FIR) spectrum determined from Stark effect measurements. We have thus recorded simultaneously the FIR pure rotation spectrum of HOCl using a Bruker IFS120HR interferometer and the spectrum of a few vibration-rotation lines in the infrared (IR) nu(2) band using a tunable diode laser spectrometer.

First Observation of the nu(17)-nu(4) Difference Bands of Diborane (10)B(2)H(6) and (11)B(2)H(6).

An analysis of the nu(17)-nu(4) difference bands near 800 cm(-1) of two isotopic species, (10)B(2)H(6) and (11)B(2)H(6), of diborane has been carried out using infrared spectra recorded with a resolution of ca. 0.003 cm(-1).

First High-Resolution Infrared Observation of the Symmetry-Forbidden nu(5) Band of (10)B(2)H(6).

Spectra of (10)B monoisotopic diborane, B(2)H(6), have been recorded at high resolution (2-3 x 10(-3) cm(-1)) by means of Fourier transform spectroscopy in the region 700-1300 cm(-1). A thorough analysis of the nu(18) a-type, nu(14) c-type, and nu(5) symmetry-forbidden band has been performed. Of particular interest are the results concerning the nu(5) symmetry-forbidden band, which is observed only because it borrows intensity through an a-type Coriolis interaction with the very strong nu(18) infrared band located approximately 350 cm(-1) higher in wavenumber.

Evidence of Vibrational-Induced Rotational Axis Switching for HD(12)C(16)O: New High-Resolution Analysis of the nu(5) and nu(6) Bands and First Analysis of the nu(4) Band (10-µm Region).

Using new high-resolution Fourier transform spectra recorded in Giessen in the 8-12 µm region, a more extended analysis of the nu(5) and nu(6) bands and the first high-resolution study of the nu(4) band of HDCO were performed. As pointed out previously [M. Allegrini, J.

High-Resolution Infrared Spectrum of the Ring-Puckering Band, nu(10), of Diborane.

The spectrum of the nu(10) band of diborane, arising from the ring-puckering vibration, has been obtained with a spectral resolution of 0.0015 cm(-1) in the region 275-400 cm(-1). The spectrum of a sample enriched in (10)B was recorded as well as one with naturally abundant boron, i.

The nu(1) and nu(3) Bands of the (17)O(16)O(17)O Isotopomer of Ozone.

Using 0.002 cm(-1) resolution Fourier transform absorption spectra of an (17)O-enriched ozone sample, an extensive analysis of the nu(3) band together with a partial identification of the nu(1) band of the (17)O(16)O(17)O isotopomer of ozone has been performed for the first time. As for other C(2v)-type ozone isotopomers [J.

High-Resolution IR Spectrum of SCF(2) from 1000 to 1400 cm(-1): The nu(1)/nu(3) + 2nu(5)/nu(2) + nu(3) and nu(4)/nu(2) + nu(5) Interacting States.

The infrared spectrum of SCF(2) was recorded in the 1000-1400 cm(-1) region with a resolution of 2.5 x 10(-3) cm(-1). The rotationally resolved nu(1) and nu(4) band systems were studied for the first time, and altogether 11 500 transitions were assigned.

The nu(2) Bands of the Deuterated Species D(2)Se and HDSe.

For the first time D(2)Se and HDSe as (80)Se monoisotopic and natural material were studied in the region of the nu(2) fundamental vibration by high-resolution (0.0033 cm(-1)) Fourier transform infrared spectroscopy. For D(2)Se which is an asymmetric rotor with C(2v) symmetry the nu(2) band is of B type while for HDSe (C(s) symmetry) it is a hybrid band, and both A- and B-type transitions were observed.

The Ground State of D(2)Se and HDSe.

Ground state rotational constants of D(M)(2)Se and HD(M)Se, M = 76, 77, 78, 80, and 82, have been determined up to octic centrifugal distortion terms from ground state combination differences. These were obtained from rotational analyses of the nu(2), nu(1), and nu(3) bands both of natural and (80)Se monoisotopic material recorded with a resolution of ca. 3 x 10(-3) cm(-1).

The High-Resolution Raman Spectrum of the nu4 Band of Diborane.

The high-resolution Raman spectra of the nu4 bands of 11B2H6 and 11B10BH6 have been recorded and analyzed. The recordings have been made using a high-resolution spectrometer based on the inverse Raman effect. Q branches have been observed, but P and R branches were too weak to be seen, and simulations of the observed band contour have been necessary to complete the analysis.

Analysis of the nu8 + nu9 Band of HNO3, Line Positions and Intensities, and Resonances Involving the v6 = v7 = 1 Dark State.

Using a high-resolution (R = 0.0025 cm-1) Fourier transform spectrum of nitric acid recorded at room temperature in the 1100-1240 cm-1 region, it has been possible to perform a more extended analysis of the nu8 + nu9 band of HNO3 centered at 1205.7075 cm-1.

The Overtone Spectrum of H2 32S near 13 200 cm-1.

The intracavity laser absorption spectrum of H2 32S has been recorded near 13 200 cm-1 with an equivalent absorption pathlength of 25 km. The observed spectrum is assigned to the (50(+/-), v2 = 1) states constituting a local mode pair in strong H22-type interaction. The rovibrational analysis has allowed the assignment of 210 lines involving 86 rotational upper state levels which have been reproduced with a rms of 0.

Absolute Line Intensities for the nu6 Band of H2O2.

The purpose of this work was to obtain reliable absolute intensities for the nu6 band of H2O2. It was undertaken because strong discrepancies exist between the different nu6 band intensities which are presently available in the literature (A. Perrin, A.