First a new perspective to study the local to normal mode transition in the series of pyramidal molecules is presented. Then a full study of the vibrational excitations of the series of pyramidal molecules XH3 with X = P, As and Sb is given in the framework of a polyad-conserving Hamiltonian of a set of interacting Morse oscillators. The model is based on an algebraic representation of the Hamiltonian in terms of su(2)-operators. A simple Hamiltonian including both Fermi and Darling–Dennison interactions is considered. For the PH3 molecule a fit involving 64 experimental energies up to polyad 8 (energies up to 9054 cm−1) provided an rms=1.74cm−1 using a Hamiltonian with 14+3(frozen) parameters. For the AsH3, with 35 experimental energies the deviation obtained was rms=2.50cm−1 with 10+4 parameters. Lastly, for the SbH3 molecule, considering 23 experimental energy levels an rms=0.86cm−1 was reached with 9+6 parameters. In all cases the polyad scheme P=2(ν1+ν3)+ν2+ν4 was considered.
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