Intensities of the v1-bands of 12CH335Cl and 12CH337Cl near 3 μm

Strengths of individual lines in the v₁ fundamental of methyl chloride have been measured at low pressure and at 296.35 K using a Fourier transform interferometer. The band strengths S_v⁰ obtained by fitting these measurements are 85.8±1.0 and 86.6±1.0 cm^-2 atm^-1 for ¹²CH₃³⁵Cl and ¹²CH₃³⁷Cl, respectively. The Q₃-branch appears to be useful for atmospheric detection of methyl chloride.     

Investigation of the reaction 37Cl(n, γ)38Cl

With Ge(Li) detectors the γ-radiation following thermal-neutron capture in natural and in ³⁷Cl enriched targets was studied. A total of 79 γ-lines has been assigned to the ³⁷Cl(n, γ) reaction and 64 of these lines have been placed in a decay scheme of ³⁸Cl. The excitation energies of 24 bound states of ³⁸Cl have been determined with 0.09–1.2 keV errors. The neutron separation energy of ³⁸Cl is 6107.7 ± 0.4 keV. A strong correlation between reduced stripping widths and (n, γ) primary reduced widths was found for the l_n(d, p) = 1 states if, instead of the Weisskopf reduction factor E_γ^?3, a factor E_γ^?1.2 was used.     

Vibrational spectra and force constants of symmetric tops: ν1, ν5, and 2ν5 of CF335Cl and CF337Cl

The gas phase infrared spectra of CF₃³⁵Cl and CF₃³⁷Cl have been recorded in the ν₁ region and 2ν₅ regions with a resolution of 0.09 cm^?1. Additionally the ν₅ fundamental of CF₃Cl, with natural isotopic abundance, has been reinvestigated with a resolution of approximately 0.36 cm^?1. Molecular constants have been evaluated from the observed spectra by means of polynomials and band contour simulation. The possibility of a Fermi resonance between ν₁ and 2ν₅ is discussed.     

Strengths of (p, γ) resonances in 33Cl, 35Cl and 28Si

Absolute strength measurements have been performed for the E_p = 580 and 588 keV ³²S(p,γ)³³Cl, E_p = 1214keV³⁴S(p,γ)³⁵Cl and E_p = 633 and 744 keV²⁷Al(p,γ)²⁸Si resonances with a Ge(Li) detector. Results are discussed with regard to the decay of isobaric analog resonances in ³⁵Cl and ³⁷Cl.     

Spin and parity assignments for 35Cl levels from the 31P(α, p)34S reaction

³⁵Cl states at excitation energies between 9.9 and 11.8 MeV have been identified through sharp resonances in the ³¹P(α, p_o)³⁴S excitation functions at 25°, 105° and 155° for E_α = 3.25–5.50 MeV. Forty-eight on-resonance angular distributions, normalized to an absolute cross section scale, have been subjected to single-level and two-level analyses resulting in spin and parity assignments for each resonance. Approximately half the resonances were of the pure single-state type, having unique angular distribution shapes. Data from 12 resonances of an earlier experiment ¹) were analyzed with the same theory, extending the diagnostics down to a ³⁵Cl excitation energy of 9.1 MeV. A set of optical potentials consistent in all four reactions that this experimental program encompasses has been incorporated in the present analysis. Validity of the optical potential is demonstrated for α-particles elastically scattered by ³¹P.     

The reaction 35Cl(n,γ)36Cl studied with non-polarized and polarized thermal neutrons

The γ-radiation following capture of non-polarized and polarized thermal neutrons in ³⁵Cl has been investigated. Of the 420 γ-rays ascribed to the ³⁵Cl(n,γ)³⁶Cl reaction, 236 have been placed in a ³⁶Cl decay scheme. The branching ratios and the excitation energies (with 0.04–0.9 keV errors) of 72 bound states have been determined. Unambiguous spin assignments are given for 11 levels. The multipole mixing ratios for some primary γ-ray transitions have been determined. There exists a significant correlation between (d, p) stripping strengths and (n, γ) reduced primary transition probabilities for transitions to l_n(d, p) = 0 levels.     

Determination of A0 for CH335Cl and CH337Cl from the ν4 infrared and Raman bands

The ν₄ infrared and Raman bands of CH₃Cl were analyzed simultaneously. A direct fit yielded a complete set of constants for CH₃³⁵Cl, including A₀ = 5.20530 ± 0.00010 cm^?1 and D_K = (8.85 ± 0.13) × 10^?5cm^?1. For CH₃³⁷Cl an incomplete set of constants was obtained from the infrared band, and A₀ = 5.2182 ± 0.0010 cm^?1 was estimated by curve fitting of the Raman spectrum. The resulting equilibrium structure is $\text{r(}\text{CH) = 1.0854 ± 0.0005}\text{A}\text{?}$, $\text{r(}\text{CCl) = 1.7760 ± 0.0003}\text{A}\text{?}$, and <(HCH) = 110°.35 ± 0°.05.     

Rotational analysis of the B3Π(0+) → X1Σ+ band systems of 35Cl35Cl and 35Cl37Cl in the chlorine afterglow emission spectrum

The B³Π(0⁺) → X¹Σ⁺ band system of Cl₂, excited by the recombination of ground state $\text{Cl}{}^2\text{P}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$ atoms at total pressures near 2 Torr, has been rotationally analyzed in the range 6300–9900 Å. About 30 bands, with 0 ≤ v′ ≤ 6 and 5 ≤ v″ ≤ 14, were investigated, mostly for both ³⁵Cl³⁵Cl and ³⁵Cl³⁷Cl. The band origins and rotational constants for the B state were obtained with the help of the known constants for the ground state. The principal molecular constants (cm^?1) for the B³Π(0⁺) state of ³⁵Cl³⁵Cl are as follows: T_e′ = 17 817.67(3); ω_e′ = 255.38(3); ω_e′x_e′ = 4.59(1); ω_e′y_e′ = ?0.038(8); D_e′ = 3341.17(14); B_e′ = 0.16313(3); α_e′ = 2.42(3) × 10^?3; γ_e′ = ?5.7(7) × 10^?5. The equilibrium internuclear separation is 2.4311(2) Å. The results of Briggs and Norrish on a transient absorption spectrum of Cl₂ assigned as $\text{0}{}_{\mathrm{g}}{}^{\mathrm{+}}\text{← B}{}^3\text{Π}\text{(0}{}^{\mathrm{+}}\text{)}$ are reinterpreted with the present constants.     

10-μm sub-doppler laser-Stark spectroscopy of methyl chloride: Analysis of the ν6 bands of the CH335Cl and CH337Cl

About 900 Stark transitions from 70 vibration-rotation transitions in CH₃³⁵Cl and about 400 transitions from 38 transitions in CH₃³⁵Cl in the ν₆ band have been assigned. These data were analyzed simultaneously with previously published microwave data on the ν₆ = 1 state. The fit has a standard deviation of about 2 MHz for the data for both isotopes. The isoptopic shift ν₆35 ? ν₆37 = 0.3766(6) cm^?1. Rotational dependence of the dipole moment was also just apparent at about μ_J = μ_K = 1 × 10^?5 D, and a complete set of molecular constants is given.     

The infrared spectra of 12C32S, 12C34S, 13C32S,and 12C33S

Using a tunable diode laser spectrometer, the infrared absorption spectra of four isotopic species of carbon monosulfide have been observed in the positive column of a dc discharge of CS₂ and Ar. The wavenumbers of 115 vibration-rotation transitions between 1180.5 and 1266.1 cm^?1 have been measured. These lines were assigned to the 1-0, 2-1, 3-2, and 4-3 bands of ¹²C³²S, the 1-0 and 2-1 bands of ¹²C³⁴S and ¹³C³²S, and the 1-0 band of ¹²C³³S. These new data have been combined with the previous infrared and microwave results to determine Dunham coefficients (Y_ij), the Dunham potential expansion constants (a₀,a₁,a₂,a₃, and a₄), and the classical turning points by the RKR method.     

Fusion reaction of 35Cl+48Ti at 104 MeV

The total fusion cross section for the system ³⁵Cl+⁴⁸Ti was measured at $\text{E}{}_{\mathrm{lab}}\text{(}{}^{35}\text{Cl}\text{) = 104}\text{MeV}$. Evaporation residues are identified by a time-of-flight mass spectrometer using a pulsed beam and solid state fission detectors. In addition, the mass yields of evaporation residues were measured by activation analysis. The results are compared to statistical model predictions.     

The ν6 band of CF235Cl37Cl from IR-MW double resonance

Effective constants for the ν₆ band of CF₂³⁵Cl³⁷Cl have been determined from the analysis of infrared-microwave double-resonance data.     

A study of the 35Cl(p, γ)36Ar reaction and the energy levels of 36Ar

Proton energies and strengths of (p,γ) and (p, p₁) resonances of the ³⁵Cl + p reaction were determined for E_p = 0.4?3.0 MeV and 1.9?3.0 MeV, respectively. The γ-decay of 84 resonances was studied with a 40 cm³ Ge(Li) detector. The branching ratios and excitation energies of 38 bound levels were determined. A new bound level was observed at E_x = 8472.0 ± 1.0 keV. Doppler-shift attenuation experiments yielded lifetimes of 20 bound levels. Spins and/or parities for bound levels and resonances were derived on the basis of observed transition strengths.     

Centrifugal distortion analysis of pure rotational spectra of H216O,H217O,and H218O

Centrifugal distortion analyses based entirely on high-quality infrared data are carried out for the ground vibrational states of H₂¹⁶O, H₂¹⁷O, and H₂¹⁸O. As a result of the analyses, the values of 27 rotation and distortion constants for each species are determined. By using these constants it was possible to improve considerably the accuracy of the literature values for rotational energy levels at high J_τ, especially for H₂¹⁷O and H₂¹⁸O. The experimental values for the energy levels are deduced from the observed rotational transitions constituting the fitted data.     

Pressure broadening in the 0–4 through 0–7 overtone bands of H35Cl and H37Cl

We have measured the pressure broadening coefficients of a number of rotation-vibration lines in the 0–4 through 0–7 overtone bands of HCl utilizing a Fourier transform spectrometer and a 409 m path length White cell. These data, when included with previous measurements on the fundamental and lower overtone bands, show a systematic variation of pressure broadening with increasing overtone band. This result reflects a change in the collision dynamics between molecules in the upper state of the transition with ground state molecules.     

Absolute wavenumber measurements of 1-0, 2-0, HF and 2-0, H35Cl,H37Cl absorption bands

Fourier absorption spectra of HCl and HF at room temperature permitted to measure 87 absolute wavenumbers. The absolute observed position of the P(6) line of the 1-0 band of HF is not in agreement with a recent heterodyne determination [3]. It is found equal to 110 725 739 ± 7.5 MHz.     

Diode laser spectrum of the ν3 band of 34SF6

A diode laser was used to measure the absorption spectrum of the ν₃ band of ³⁴SF₆. This isotopic species, which is present in the natural sample (4.2%), was cooled in a molecular beam of pure SF₆. Subbranches up to J = 22 were recorded and identified. The molecular parameters, determined with a simple fitting procedure, are compared with those known of ³²SF₆ and ³³SF₆.     

Parity non-conservation in the radiative capture of polarized neutrons by 35Cl

We report a measurement of the forward-backward asymmetry in the radiative capture of polarized cold neutrons in the reaction ³⁵Cl(n, γ)³⁶Cl where ³⁶Cl is in the ground state. The measured value of the asymmetry is a = (1.57 ± 0.531) × 10^?4. We deduce the mixing between the 2⁺ capture level and the neighboring 2^? levelto be $\text{〈2}{}^{\mathrm{?}}\text{¦H}{}_{\mathrm{<mtext>p.v.</mtext>}}\text{¦2}{}^{\mathrm{+}}\text{〉 = ?0.25 ± 0.08}\text{eV}$ before corrections. A measurement of the integral asymmetry of all γ-rays in the neutron capture by ³⁵Cl leads to agreement with measurements at Leningrad.     

Étude des États excités du 33Cl à l′aide de la réaction 32S(p, γ)33Cl

Energies and strengths of resonances of the ³²S(p, γ)³³Cl reaction were determined in the range E_p = 0.4 ? 2.6 MeV. Three new resonances were observed respectively at E_p = 1588, 1748, 1880 keV and the doublet of resonances at E_p ≈ 1900 keV was clearly shown. The (p, γ) strengths of resonances at E_p = 422, 580, 588, 721 and 2577 keV were measured with a 80 cm³ Ge(li) detector. The Q-value of this reaction and the energies, γ-ray branchings and mean lifetimes of levels were determined. The spins and parities of the E_x = 2.35, 3.82, 3.97, 3.98, 4.78 MeV levels have been measured. A comparison of γ-ray transition strengths with mirror transitions and with model predictions is made.