We present high-resolution spectroscopy of Rb2 ultralong-range
Rydberg molecules bound by mixed singlet-triplet electron-neutral atom
scattering. The mixing of the scattering channels is a consequence of the
hyperfine interaction in the ground-state atom, as predicted recently by
Anderson et al. \cite{Anderson2014b}. Our experimental data enables the
determination of the effective zero-energy singlet s-wave scattering length
for Rb. We show that an external magnetic field can tune the contributions of
the singlet and the triplet scattering channels and therefore the binding
energies of the observed molecules. This mixing of molecular states via the
magnetic field results in observed shifts of the molecular line which differ
from the Zeeman shift of the asymptotic atomic states. Finally, we calculate
molecular potentials using a full diagonalization approach including the
p-wave contribution and all orders in the relative momentum k, and compare
the obtained molecular binding energies to the experimental data