Overtone spectroscopy of some benzaldehyde derivatives

Overtone spectrum of o, m and p-nitrobenzaldehydes and p-chlorobenzaldehyde has been studied in 2000–12000 cm⁻¹ region. Vibrational frequencies and anharmonicity constants for aryl as well as alkyl CH stretch vibrations have been determined. We have also determined the internuclear distances for the aryl CH bond in the different molecules. The small variation observed in these distances is an indication of the substitution effect. It is observed that in the case of p-disubstituted benzens, the shift in aryl CH bond is proportional to sum of the Hammet σ of the substituents. However in the case of o-disubstituted benzenes it is only 80% of the para-substituted shift.     

Overtone spectra of styrene and polystyrene in the visible and near infrared regions

Vibrational overtone spectra of styrene (liquid) and polystyrene (solid), studied by the laser-induced thermal lens (for ΔV=6) and the conventional near infrared absorption (for ΔV=3–5) techniques, are reported. For polystyrene, the overtone energy-bond length correlation predicts that the aryl CH bonds are ～0.0005 Å longer than that in benzene, while no such conclusions could be drawn on styrene. Thesp ³ CH overtones in polystyrene are observed on the low energy side of the aryl CH overtones.     

Overtone singing: Productive mechanisms and acoustic data

Overtone singing is where one person sings in two voices, the first voice represented by the fundamental and the second by an enhanced harmonic. Overtone singing is performed in chest register. Tuning of the first or second formant and a reduction of the formant bandwidth down to 20 Hz make harmonics prominent. Narrowing the pharynx, velar constriction, variation of the small mouth opening, and a tension of the walls of the mouth cavity are used. Changing prominent harmonics has the effect of creating an overtone melody with sustained tones, tone steps, and trillos.     

Diode laser spectroscopy of CO2 at 790 nm

Absorption lines of ¹²C¹⁶O₂ have been examined by using a tunable diode laser spectrometer in the region around (790 nm). The spectrometer sources are commercially available double heterostructure InGaAlAs tunable diode lasers (TDLs) operating in the “free-running” mode, which allowed the detection of the line positions within . The observed carbon dioxide absorption lines belong to the combination overtone 2ν₂+5ν₃ ro-vibrational band with intensities ranging around .     

Neon matrix isolation spectroscopy of CO2 isotopologues

The solid neon matrix isolated spectrum of CO₂ are recorded in the 2–5 μm region. Natural and ¹³C or ¹⁸O enriched CO₂ samples were used and the nν₁ + ν₃ (n = 0, 1, 2) series bands of different CO₂ isotopologues have been observed. The solid neon matrix shift due to Fermi-resonance of bands within the same vibrational polyad is analyzed.     

Diode laser overtone spectroscopy of CO2 at 780 nm

Overtone absorption lines of ¹²C¹⁶O₂ have been examined by using a tunable diode laser (TDL) spectrometer in the region around . The spectrometer sources are commercially available double heterostructure InGaAlAs TDLs operating in the “free-running” mode, which allowed the detection of the line positions within . The observed carbon dioxide absorption lines belong to the ν₁+5ν₃ ro-vibrational band with rotational quantum number J up to 48. The minimum absorbance detected by the spectrometer (?5×10^-6) permitted to observe the weakest lines having the absorption cross section of the order of .     

CH local mode overtone excitations in benzyl chloride—A conformational study

The CH local mode overtone spectrum of benzyl chloride in the visible and NIR regions studied by laser induced thermal lens and conventional NIR absorption is presented. The analysis shows that the −CH₂Cl group is symmetrically oriented with respect to the benzene ring, thus finalizing one of the two possible conformational models predicted by electron diffraction studies. The aryl CH bonds have a slightly larger force constant than that in benzene.     

Methane diode laser overtone spectroscopy at 840 nm

Overtone absorption lines of ¹²CH₄ have been examined by using a tunable diode laser (TDL) spectrometer in the region around (840 nm) where the combination overtone band ν₁+3ν₃ lies. The spectrometer sources are commercially available heterostructure GaAlAs TDLs operating in the “free-running” mode, which allowed the detection of the line positions within . The wavelength modulation spectroscopy (WMS) and the second harmonic detection technique permitted the measurements of minimum absorbances of the order of ?5×10^-6. This allowed to observe the weakest lines of the band with absorption cross-sections of the order of ?2×10^-25 cm²/molecule or /amagat. For some of them self-, air-, He- and H₂-broadening coefficients have been obtained at room temperature.     

High-resolution diode laser absorption spectroscopy of the O-H stretch overtone band (2,0,0)←(0,0,0) of the HO2 radical

The O-H stretching overtone (2ν₁) of the HO₂ radical was observed between 6603.2 to by using tunable diode laser absorption spectroscopy (TDLAS). About 1000 lines were observed in this region of which 491 transitions could be definitively assigned to the 2ν₁. The spectrum is observed to be an A/B hybrid band with band features of both a perpendicular and parallel nature. Transitions of the A-type bands with K_a^′=0-3, N^′?16 and transitions of the B-type bands with K_a^′=0,1, N^′?15 were assigned. The origin calculated from the best fit to the present spectrum is at which is ∼ higher than previously reported. The overtone spectrum is observed to be heavily perturbed, possibly by Fermi resonance with energy levels of the nearby (ν₂+5ν₃) state.     

Diode laser spectroscopy of ethylene overtones at 830 nm

A tunable diode laser spectrometer has been employed to examine the 3rd overtone absorption lines of C₂H₄ at around 12 000 cm⁻¹ (830 nm). The spectrometer sources are heterostructure AlGaAs tunable diode lasers operating “free-running”. By the aid of the wavelength modulation spectroscopy with the second harmonic detection technique and a Herriott type multipass cell 63 very weak absorption lines have been observed for the first time, with cross sections as low as 2 × 10⁻²⁶ cm²/mol, equivalent to . The self-broadening coefficient has been measured for one of the most intense lines.     

History of spectroscopy and modern micromachined disposable Si ATR-IR spectroscopy

In this article, the historical development of spectroscopy is examined and the spectroscopy devices used today are described. Then, we focus on infrared (IR) spectroscopy, which cannot give valuable signal in aqueous solution. Attenuated total reflection (ATR)-IR technique solves the problem. In addition, we specifically mention newly developed disposable ATR-IR crystals and micromachined silicon (Si) ATR-IR. Disposable crystal systems and microfluidics systems can be integrated with existing miniature ATR analyzers. If the integration is successful, the technique might be used in biomedical measuring instruments, reactions' analyses, and ultra-high-pressure analyses.     

Overtone vibrations of molecules

A vibrational equation for overtones is derived by applying the direct multiplication of matrices in the framework of the molecular vibration theory. The relationships determining the characteristics of the overtone vibration mode and expressions describing the changes in the structural and geometric molecular parameters are obtained by solving the deduced equation. The electro-optical parameters of the overtones 2ν_s, 3ν_s, 4ν_s, and 5ν_s(s=3, 4) of a methane molecule are calculated from the deduced relationships using the semiempirical quantum-mechanical CNDO/2 method and numerical differentiation with cubic spline functions.     

Overtone spectroscopy of water molecules based on room temperature diode laser emitting in the NIR range

The measurement of very weak overtone spectroscopic line shape of water molecule is performed using wavelength modulation spectroscopy (WMS). In this work a high resolution near infrared diode laser spectrometer is used to record first derivative (1f) signal of buffer gas Helium and Carbon dioxide broadened water vapour transitions around 820 nm wavelength region. The effect of collision due to perturber pressure on signal to noise ratio (SNR) is discussed. The Lorentzian HWHM of observed 1f signal is calculated. The comparison is made between collisional broadening of water vapour transition broadened by inert gas Helium and high quadrupole moment active gas Carbon dioxide.     

X射线光电子能谱

X射线光电子能谱（X-ray photoelectron spectroscopy，XPS）技术也被称作用于化学分析的电子能谱（electron spectroscopy for chemical analysis，ESCA）．XPS属表面分析法，它可以给出固体样品表面所含的元素种类、化学组成以及有关的电子结构重要信息，在各种固体材料的基础研究和实际应用中起着重要的作用．文章简要介绍了XPS仪器的工作原理和分析方法，并给出了XPS在科学研究工作中的应用实例．     

Laser spectroscopy of stable Os isotopes

Doppler-free isotope shift measurements of the stable even ^184–192Os and ^187,189Os odd isotopes have been performed for the first time on the 5d ⁶6s ^{2 5}D₄→5d ⁶6s6p ⁷F₄ (305.9 nm) transition in the neutral atom by atomic beam laser spectroscopy and on the ionic 5d ⁶6s ⁵D_9/2→5d ⁶6p ⁶D_7/2 (228.2 nm) transition by fast collinear ion-laser spectroscopy. The measurements were carried out in Manchester and at the IGISOL facility in Jyväskylä in Finland, respectively. The results presented are the most precise measurements to-date of the absolute isotope shifts.     

Fourier spectroscopy of the stratospheric emission

Emission spectra of the stratosphere have been recorded from balloon altitude with an unapodized resolution of 0.0033 cm^–1 in the submillimeter (SM) spectral range. Preliminary results on constituent identification are presented in this paper.     

Rotational spectroscopy of the first excited state of the acetylenic C-H stretch of 3-fluoropropyne performed by infrared-Fourier transform microwave-microwave triple-resonance spectroscopy

The rotational spectra of 3-fluoropropyne in the ground and first excited acetylenic C-H stretch vibrational state have been measured. The pure rotational spectrum of the normal species and the ¹³C isotopomers were measured using FTMW-cwMW double-resonance spectroscopy based on the Autler-Townes (AC Stark) effect. The lineshape properties of this measurement make it possible to determine the transition strength, ΔJ-selection rules, and the relative energy ordering of the quantum states. The frequency accuracy of this technique is tested against a previous pure rotational study of 3-fluoropropyne. The rotational spectrum of vibrationally excited state was obtained through IR-FTMW-cwMW methods. In this technique a single-longitudinal-mode pulsed infrared laser source vibrationally excites the acetylenic C-H stretch with J-selectivity. The rotational spectrum of the excited state is then obtained by FTMW and FTMW-cwMW double-resonance methods. The excited-state measurements have a signal-to-noise ratio comparable to the pure rotational spectrum. The residuals in the excited-state fit are larger than those obtained in the ground-state fit. This greater deviation from a standard asymmetric top spectrum is most likely due to weak perturbations to the acetylenic C-H spectrum.