We predict level degeneracy of the rotational type in diatomic molecules
described by means of a cotangent-hindered rigid rotator. The problem is shown
to be exactly solvable in terms of non-classical Romanovski polynomials. The
energies of such a system are linear combinations of t(t+1) and 1/[t(t+1)+1/4]
terms with the non-negative integer principal quantum number t=n+|/bar{m}|
being the sum of the degree n of the polynomials and the absolute value,
|/bar{m}|, of the square root of the separation constant between the polar and
azimuthal motions. The latter obeys, with respect to t, the same branching
rule, |/bar{m}|=0,1,..., t, as does the magnetic quantum number with respect to
the angular momentum, l, and, in this fashion, the t quantum number presents
itself indistinguishable from l. In effect, the spectrum of the hindered
rotator has the same (2t+1)-fold level multiplicity as the unperturbed one. For
small t values, the wave functions and excitation energies of the perturbed
rotator differ from the ordinary spherical harmonics, and the l(l+1) law,
respectively, while approaching them asymptotically with increasing t. In this
fashion the breaking of the rotational symmetry at the level of the
representation functions is opaqued by the level degeneracy. The model provides
a tool for the description of rotational bands with anomalously large gaps
between the ground state and its first excitation.Comment: 10 pages, 6 figures; Molecular Physics 201