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Nuclear Data Sheets for A = 127

The 1996 evaluation for the A=127 mass chain (1996Ki01) has been revised. The experimental results from various decays and reactions for the A=127 mass chain have been compiled and evaluated. The nuclides covered in this evaluation are from {sup 127}Ag to {sup 127}Nd. The data are summarized and presented, together with adopted level schemes.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Absolute frequency measurements for emission transitions of molecular iodine in the range of 1053 – 1068 nm

Results of high-precision frequency measurements are presented for certain components of the {sup 127}I{sub 2} hyperfine structure, which correspond to emission transitions of the B – X band in the range of 1053 – 1068 nm. The frequencies are measured by using a femtosecond optical frequency synthesiser based on a Ti:sapphire laser. The hyperfine structure is resolved by the method of three-level laser spectroscopy. The frequency-doubled cw Nd : YAG laser is used as an excitation radiation source, and the probe radiation in the range of 1050 – 1070 nm is generated by an external-cavity diode laser. The frequencies of both lasers are simultaneously locked to those of two adjacent hyperfine structure components of iodine lines, which have a common upper level. Correspondingly, the frequency of the Nd : YAG laser is locked to the frequency of the absorption transition component, and the diode laser frequency – to the frequency of the emission transition component. The radiation frequency of the diode laser ‘locked’ in this way is measured. Frequencies of 18 hyperfine structure components for six emission lines corresponding to the bands (32 – 54) and (32 – 53) are measured. The relative uncertainty of the measurement is 8 × 10{sup –10}. (paper)

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Absolute frequency measurement for the emission transitions of molecular iodine in the 982 - 985 nm range

We report high-precision frequency measurements of the separate hyperfine structure (HFS) components of the emission B - X system transitions of {sup 127}I{sub 2} molecules in the 982 - 985 nm range. To resolve the HFS of the emission lines, advantage was taken of the method of three-level laser spectroscopy. The function of exciting radiation was fulfilled by the second harmonic of a cw Nd : YAG laser, and the probe radiation in the 968 - 998 nm range was generated by an external-cavity diode laser. The output Nd : YAG laser frequency was locked to an HFS component of the absorption transition and the probing laser radiation to the emission transition component. When both frequencies were locked to HFS components with a common upper level, the output diode laser frequency was precisely equal to the emission transition frequency. The output frequency of the thus stabilised diode laser was measured with the help of a femtosecond optical frequency synthesiser based on a Ti : sapphire laser. We present the results of the absolute frequency measurements of 20 HFS components belonging to six vibrational - rotational transitions of the B - X system of iodine [R56(32 - 48)a1, P58(32 - 48)a1, P85(33 - 48)a1, R87(33 - 48a1, R88(33 - 48)a10] and all 15 components of the R86(33 - 48) line. The relative measurement uncertainty is equal to 7 Multiplication-Sign 10{sup -10} and is determined by the frequency instability of the diode laser radiation.

74 ATOMIC AND MOLECULAR PHYSICS↗