The a-Type K = 0 Microwave Spectrum of the Methanol Dimer

The rotational spectrum of (CH₃OH)₂ has been observed in the region 4-22 GHz with pulsed-beam Fabry-Perot cavity Fourier-transform microwave spectrometers at NIST and at the University of Kiel. Each a-type R(J), K_a = 0 transition is split into 15 states by tunneling motions for (CH₃OH)₂, (¹³CH₃OH)₂, (CH₃OD)₂, (CD₃OH)₂, and (CD₃OH)₂. The preliminary analysis of the methyl internal rotation presented here was guided by the previously developed multidimensional tunneling theory which predicts 16 tunneling components for each R(J) transition from 25 distinct tunneling motions. Several isotopically mixed dimers of methanol have also been measured, namely ¹³CH₃OH, CH₃OD, CD₃OH, and CD₃OD bound to ¹²CH₃OH. Since the hydrogen bond interchange motion (which converts a donor into an acceptor) would produce a new and less favorable conformation from an energy viewpoint, it does not occur and only 10 tunneling components are observed for these mixed dimers. The structure of the complex is similar to that of water dimer with a hydrogen bond distance of 2.035 Å and a tilt of the acceptor methanol of 84° from the O-H-O axis. The effective barrier to internal rotation for the donor methyl group of (CH₃OH)₂ is ν₃ = 183.0 cm⁻¹ and is one-half of the value for the methanol monomer (370 cm⁻¹), while the barrier to internal rotation of the acceptor methyl group is 120 cm⁻¹.     

Force field calculations of acetonitrile using CNDO/force method

The redundancy-free internal valence force field (RFIVFF) of acetonitrile is reported using CNDO/force method. The initial force field is set up by taking the interaction and bending force constants from CNDO force field and transferring stretching force constants from the force fields of chemically related molecules. The final force field is obtained by refining the initial force field using vibrational harmonic frequencies of CH₃CN,¹³CH₃CN, CH₃ ¹³CN, CH₃C¹⁵N, CD₃CN and CD₃ ¹³CN. The final force field thus obtained is found to be excellent on the basis of frequency fit and potential energy distribution.     

Calculation of spectroscopic parameters and vibrational overtones of methanol

A high-level quartic ab initio potential energy surface of methanol has been used to calculate spectroscopic constants of the ¹²CH₃OH molecule. These include coefficients of quartic anharmonic resonance terms, Darling-Dennison constants, for stretching states. A model expressed in terms of dimensionless normal coordinates has been employed in the calculation of O—H and C—H stretching vibrational states in high-overtone regions. Both cubic Fermi and quartic Darling-Dennison anharmonic coupling terms have been included in the model in order to take into account strong resonances between different states. The nonlinear least-squares method has been used to optimize some of the model parameters employing experimental term values of ¹²CH₃OH as data. Vibrational assignments are suggested for the first C—H stretching overtone region.     

Far infrared laser lines produced by methanol and its isotopic species: A review

Methanol (CH₃OH) is considered today one of the most important active media for the generation of laser radiation in the far-infrared (FIR) spectral region. Together with ten of its other isotopic species, it is responsible for the major part of the laser lines generated by the optical pumping technique. Due to the extreme importance of those molecules as laser generators, we understood that there was a necessity of a comprehensive work which would include as much pratical information as possible about each line.Chang et al⁽¹⁾ early recognized methanol as a source of strong FIR laser lines. Since then, more than 100 papers were published containing information about new laser emission. Recently, Moruzzi et al⁽¹¹⁴⁾ presented a review of 575 lines produced by¹²CH₃OH. In the present paper, we have extended the review to the various isotopic modifications of this molecule (namely¹³CH₃OH, CD₃OH,¹³CD₃OH, CD₃OD,¹³CD₃OD, CH₃OD, CH ₃ ¹⁸ OH, CH₂DOH, CH₂DOD and CHD₂OH), a total of nearly 2000 lines with wavelengths ranging from 19µm to 3030µm.     

A review of optically pumped far-infrared laser lines from methanol isotopes

The technique of optical pumping in polar molecules is the most efficient for Far-Infrared (FIR) laser generation, providing also a versatile and powerful tool for molecular spectroscopy in this spectral region. Methanol (CH₃OH) and its isotopic varieties are the best media for optically pumped FIR laser, with over thousand lines observed, and the most widely used for investigations and applications. In this sense, it is important organize and make available catalogues of FIR laser lines as complete as possible. Since the last critical reviews of 1984 [1] on methanol and its isotopic varieties [2,3,4], over hundred papers have been published dealing with hundreds of new FIR laser lines. In 1992 a review of FIR laser lines from CH₃OH was presented [5]. In this communication we extend this work to the other methanol isotopes, namely CH₃OD, CD₃OH, CD₃OD,¹³CH₃OH,¹³CD₃OH,¹³CD₃OD, CH₃ ¹⁸OH, CH₂DOH, CHD₂OH and CH₂DOD.Work supported by FAPESP, CNPq, FAEP-Brasil, and CNR-Italia     

Spectroscopy of Methanol and Its Application to Optically Pumped THz FIR Lasers

In this paper, we have reviewed the details of experimental and theoretical aspects of the high-resolution molecular spectroscopy of methanol isotopomers. The methods of spectroscopic assignments and analysis have been discussed. The applications of the spectroscopic techniques, particularly of Fourier transform spectroscopy in the field of optically pumped Terra-Hertz Lasers (OPTL) and far infrared (OPFIR) lasers have been discussed. New assignments have been deduced for TEA-CO₂ laser pumped methanol and CW CO₂ pumped ¹³CD₃OD. Stark effect analyses and the determination of accurate dipole moment values have been discussed for CH₃OH, ¹³CH₃OH and CH₃ ¹⁸0H. The importance of high-resolution spectroscopy is also discussed in terms of astrophysical detection. Some recent ongoing astrophysical efforts are outlined. In our laboratory we are in the process of setting up a THz methanol laser for astrophysical applications and search for new coherent monochromatic laser sources.     

Determination of force fields for two conformers of nitromethane bycndo/Force method

cndo/Force method is used to evaluate the redundancy free internal valence force fields for two conformers of nitromethane. The initial force field is set up by taking the interaction and bending force constants from this method and transferring the stretching force constants from the force fields of chemically related molecules. The final force field is obtained by refining the initial force field using vibrational frequencies of isotopic speciesviz CH₃NO₂, CD₃NO₂, CH₃ ¹⁵NO₂ and CH₃N¹⁸O₂. The final force field thus obtained is reasonable on the basis of frequency fit and potential energy distribution. The barrier to internal rotation is found to be 0.048 kcal mol⁻¹.     

An experimental approach to the analysis of electric field gradients in ionic crystals

The spectrum of a partially oriented sample of ethanol has been analysed by making use of the simpler spectra obtained from the species CD₃CH₂OH and CH₃CD₂OH, together with ¹H?{²H} double resonance. With p-ethoxy-benzylidene-p-n-butylaniline (EBBA) as the nematic solvent the dipolar couplings of CH₃ and CH₂ protons with the OH proton can be observed, and their magnitudes are compared with values calculated assuming different models for C-O-H internal rotation. Information on the quadrupole coupling constant tensor elements for CD₃ and CD₂ deuterium nuclei is obtained.     

Pure Rotational Raman Spectra of Vapor Phase Methanols

Abstract

The rotational Raman spectra of four vapor phase isotopic methanols, CH₃OH, CH₃OD, CD₃OH and CD₃OD, have been reported for the first time in the wavenumber regions from 5 to 100–120 cm^?1. The major parts of the spectra consist of bands equispaced at 3.19, 3.04, 2.56 and 2.46 cm^?1 intervals, respectively, and have been interpreted as the pure rotational S-branch transitions.     

Vibration-rotation effects on the polarizabilities of CH4 and CD4 calculated from an ab initio polarizability surface

A polarizability surface has been calculated for the methane molecule using a Hartree-Fock wavefunction. Coefficients of the surface are given to second order in terms of both symmetry coordinates and internal coordinates. The polarizability is sensitive to bond stretching and angle bending. The effects of nuclear motion on the polarizabilitles of ¹²CH₄ and ¹²CD₄ have been calculated from the coefficients of the surface. Some of the second order coefficients are found to be significant in contributing to the nuclear motion corrections. The ν₃ mode is the dominant contributor to the corrections. The temperature dependences of the mean molecular polarizabilities of ¹²CH₄ and ¹²CD₄ are also calculated. The results suggest that modern methods of measurement could distinguish between the isotopomers CH_4-n D _n (n=0–4) thereby enabling an experimental surface to be obtained.     

Frequency and efficiency measurements on FIR laser lines close to the N+ 3 P 2−3 P 1 transition

FIR laser lines close to the N^{+ 3} P ₂–³ P ₁ transition at 122 m can be used as a local oscillator for heterodyne detectors. The frequencies of some candidate laser lines from CH₂F₂,¹³CH₃OH, CD₃OD, and CD₃OH have been measured and the output power of the most interesting lines has been optimized.     

The methyl bromide molecule: A critical consideration of perturbations in spectra

This work gives an extensive critique of studies on methyl bromide and all its isotopic varieties with special stress on their rotational, vibrational, and rovibrational spectra. The rotational constants of more than 40 vibrational states of CH₃Br and 20 of CD₃Br, as well as of the ground states of all varieties, were critically examined and corrected where needed. An almost complete set of harmonic and anharmonic constants for CH₃Br was derived. From the set of rotation-vibration interaction constants, new accurate equilibrium constants A_e and B_e have been evaluated for CH₃⁷⁹Br, CH₃⁸¹Br, CD₃⁷⁹Br, CD₃⁸¹Br, from which the following equilibrium structure is obtained: r_e(C---H) = 1.0823 Å; r_e(C---Br) = 1.9340 Å; α(HCH) = 111.157°.     

The anharmonic force field and equilibrium structure of methane

The anharmonic force field of methane has been refined to fit spectroscopic data from the isotopic species ¹²CH₄, ¹³CH₄, ¹²CH₄, ¹²CH₃D, ¹²CHD₃ and ¹²CH₂D₂. Six of the thirteen cubic force constants have been determined experimentally, the remaining cubic constants being fixed at values derived from ab initio calculations. The quartic force field is very crude, in that only f_rrrr has been refined. It is concluded however that the cubic and quartic force fields, even though they are subject to limitations, provide a considerable improvement in the experimental determination of the r _e structure and the quadratic force field. The equilibrium bond length is found to be r _e(CH) = 1·085₈ ± 0·001 Å.     

Fundamental vibrational frequencies and spectroscopic constants for the methylperoxyl radical,CH3O2, and related isotopologues 13CH3OO,CH3 18O18O,and CD3OO

Accurate spectroscopic and geometric constants for CH₃O₂, and its isotopologues ¹³CH₃OO, CH₃ ¹⁸O¹⁸O and CD₃OO, are predicted. Employing coupled cluster theory with single, double, and perturbative triple excitations [CCSD(T)], we obtain optimized equilibrium geometries using Dunning's cc-pVTZ basis set. A Taylor expansion of the potential energy surface, including all third-order and semidiagonal fourth-order terms in a basis of normal coordinates, yields anharmonic vibrational frequencies and vibrationally-averaged properties including the effects of anharmonicity. We detail the strong influence of Fermi resonances on the problematic ν₆ vibrational mode of CD₃OO, arriving at a value of 993?cm^?1; two previous experimental measurements of this mode appear to have been incorrectly assigned. Our computed energies for the low intensity ν₁₁ transition are in excellent agreement with experimental measurements performed for CH₃ ¹⁸O¹⁸O and CD₃OO, inspiring confidence that our results will serve as a guide for experimental measurement of this yet-unobserved quantity for the CH₃OO and ¹³CH₃OO isotopologues. Given the reliability of our force field, and considering the results of other experiments, we make a number of reassignments to previously recorded spectra, which eliminate large disagreements between experimental observations. The vibrational averaging of the rotational constants and geometries are also discussed for each isotopologue.     

New FIR laser lines from an optically pumped far-infrared laser with isotopic 13C16O2 pumping

A ¹³C¹⁶O₂ laser optically pumping a FIR laser has resulted in 17 new FIR cw emissions from 78.5 μm to 917 μm. The FIR media were: CD₃OD, CH₃OD, CD₃OH, NH₃ and ¹⁵NH₃. Interesting effects have been observed with a combination of NH₃ and CD₃OD resulting in a new FIR emission. Two new FIR emissions at 181.5 μm and 355.5 μm have been observed with a ¹²C¹⁶O₂ laser optically pumping CD₃OD.     

Harmonic Frequencies and Potential Energy Distributions of Partially Deuterated Methyl Cyanide

Although the vibrational spectra and force constants of CH₃CN and CD₃CN have been thoroughly studied, partially deuterated methyl cyanide has received much less attention. The infrared spectrum of CD₂HCN has only recently been reported1 and that of CH2DCN has not yet appeared. Normal coordinate analysis for neither partially deuterated species has appeared. We report here harmonic frequencies and potential energy distributions for both partially deuterated methyl cyanide species, CH₂DCN and CD₂HCN, based on force fields and structural parameters from CH₃CN and CD₃CN. The calculated frequencies for CD₂HCN are compared with the observed infrared frequencies. The vibrational interaction of the relatively high CN stretching frequency and the CD stretching frequencies is also discussed.     

用从头算方法研究GeCl2分子的非谐振力场和光谱常数

用从头算方法的MP2和CCSD（T）方法结合cc-pVTZ基组计算了二氯化锗同位素（⁷⁰GeCl₂、⁷²GeCl₂和⁷⁶GeCl₂）分子的平衡结构、光谱常数和非谐振力场.二氯化锗的几何结构、转动常数、振转相互作用常数、谐频、非谐振常数、四次和六次离心畸变常数、三次和四次力常数的计算结果与实验结果符合较好,二氯化锗分子的同位素效应较小,可能的原因是Ge同位素的质量变化相对较小.两种方法计算的结果均与实验结果符合,但CCSD（T）方法比MP2计算结果的偏差稍大一些,可能的原因是CCSD（T）方法在描述过共价Cl原子的电子相关时不够充分.     

High-resolution photoelectron spectroscopy of methanol and its deuterated derivatives: Internal rotation in the ground ionic state

The He(I) photoelectron spectra of CH₃OH, CH₃OD and CD₃OD have been measured and subjected to a deconvolution procedure in order to improve     

Quantum dynamics study of isotope effects of the OD/OH + CH3 reactions

ABSTRACT

A six-degrees-of-freedom, time-dependent quantum dynamics calculation is employed to study the integral cross sections, full-dimensional cumulative reaction probabilities and full-dimensional rate constants for the isotopic reactions of the OD and OH with CH₃ reactions. The full-dimensional cumulative reaction probabilities and full-dimensional rate constants are obtained using the energy and J-K shifting approaches based on the six-degrees-of-freedom calculations. The comparison of integral cross sections shows that the OD?+?CH₃ reaction has a larger energy threshold and a smaller tunnelling effect than the OH?+?CH₃ reaction. The corrected rate constants using the experimental zero-point energy have a very good agreement with the experimental results. The comparison of the rate constants shows that the OD?+?CH₃ has smaller rate constants than the OH?+?CH₃ reaction, which indicates a smaller reactivity due to the isotope substitution.