Abstract

The products of the two and three bipolar harmonics YLMℓ1ℓ2(r31,r32){\cal Y}^{\ell_1 \ell_2}_{LM}({\bf r}_{31}, {\bf r}_{32}) are represented as the finite sums of powers of the three relative coordinates r32,r31r_{32}, r_{31} and r21r_{21}. The complete (angular+radial) integrals of the products of the two and three bipolar harmonics in the basis of exponential radial functions are expressed as finite sums of the auxiliary three-particle integrals Γn,k,l(α,β,γ)Γ_{n,k,l}(α, β, γ). The formulas derived in this study can be used to accelerate highly accurate computations of the rotationally excited (bound) states in arbitrary three-body systems. In particular, we have constructed compact (400-term) variational wave functions for the triplet and singlet 2P(L=1)−2P(L = 1)-states in light two-electron atoms and ions. Highly accurate calculations (20 - 21 stable decimal digits in the total energy) of the triplet and singlet 2P(L=1)−2P(L = 1)-states in the two-electron Li+^{+}, Be2+^{2+}, B3+^{3+} and C4+^{4+} ions are performed for the first time

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