The states 1^1\Sigma^+_u, 1^1\Pi_u and 2^1\Sigma^+_u of Sr_2 studied by Fourier-transform spectroscopy

A high resolution study of the electronic states 1^1\Sigma^+_u and 1^1\Pi_u which belong to the asymptote 4^1D + 5^1S and of the state 2(A)^1\Sigma^+_u, which correlates to the asymptote 5^1P + 5^1S, is performed by Fourier-transform spectroscopy of fluorescence progressions induced by single frequency laser excitation. Precise descriptions of the potentials up to 2000 cm^{-1} above the bottom are derived and compared to currently available ab initio calculations. Especially for the state 1^1\Sigma^+_u large deviations are found. Rather weak and local perturbations are observed for the states 1^1\Pi_u and 2^1\Sigma^+_u, while a strong coupling of the state 1^1\Sigma^+_u to the component \Omega=0^+_u of the state 1^3\Pi_u, which belongs to the asymptote 5^3P + 5^1S, is indicated.Comment: Typing errors corrected (including numbers in table IX), 12 pages, 9 figure

Study of the Born-Oppenheimer Approximation for Mass-Scaling of Cold Collision Properties

Asymptotic levels of the A $^1\Sigma_u^+$ state of the two isotopomers $^{39}{\rm K}_2$ and $^{39}{\rm K}^{41}{\rm K}$ up to the dissociation limit are investigated with a Doppler-free high resolution laser-spectroscopic experiment in a molecular beam. The observed level structure can be reproduced correctly only if a mass dependent correction term is introduced for the interaction potential. The applied relative correction in the depth of the potential is $10^{-6}$, which is in the order of magnitude expected for corrections of the Born-Oppenheimer approximation. A similar change in ground state potentials might lead to significant changes of mass-scaled properties describing cold collisions like the s-wave scattering length.Comment: 8 pages, 6 figure

Mixing of 0(+) and 0(-) observed in the hyperfine and Zeeman structure of ultracold Rb-2 molecules

We study the combination of the hyperfine and Zeeman structure in the spin-orbit coupled A(1)Sigma(+)(u) = b(3)Pi(u) complex of Rb-87(2). For this purpose, absorption spectroscopy at a magnetic field around B = 1000 G is carried out. We drive optical dipole transitions from the lowest rotational state of an ultracold Feshbach molecule to various vibrational levels with 0(+) symmetry of the A - b complex. In contrast to previous measurements with rotationally excited alkali-dimers, we do not observe equal spacings of the hyperfine levels. In addition, the spectra vary substantially for different vibrational quantum numbers, and exhibit large splittings of up to 160 MHz, unexpected for 0(+) states. The level structure is explained to be a result of the repulsion between the states 0(+) and 0(-) of b(3)Pi(u), coupled via hyperfine and Zeeman interactions. In general, 0(-) and 0(+) have a spin-orbit induced energy spacing Delta, that is different for the individual vibrational states. From each measured spectrum we are able to extract Delta, which otherwise is not easily accessible in conventional spectroscopy schemes. We obtain values of Delta in the range of +/- 100 GHz which can be described by coupled channel calculations if a spin-orbit coupling is introduced that is different for 0(-) and 0(+) of b(3)Pi(u).DFGMinistry of Science and Culture of Lower Saxony, German