Cesanite was originally determined by Tazzoli (1983) to be
isotypic to that of
hydroxylapatite. This was determined by refining the original
unit cell dimensions and comparing them to the atomic coordinates of Holly Springs hydroxylapatite. From this it was extrapolated that although different
elements are substituted for cesanite, the structure and cell parameters are nearly the same with some differences in the
bond lengths of the
tetrahedra. This similarity was to confirm the
space group P3/m previously assigned to cesanite, this changed in 2002 after a reexamination of cesanite by Piotrowski et al. was prompted by its similarities to a synthetically produced
analog. After this study it was found that the
crystal structure of cesanite to be
isostructural to this
synthetic analog with the chemical formula Ca2Na3[(OH)(SO4)3]. What can be inferred from this is that while hydroxylapatite remains similar in its chemical formula it is not longer to be considered a structural analog. The new correct space group is
P. It can be inferred that the reason the mistake went unnoticed for so long is that cesanite retains
pseudo-symmetry in the array of its tetrahedra that closely mimics
P3/m. Cesanite's crystal structure is made up of tetrahedra of
sulfide cations surrounded by
oxygen anions distributed along with
hydroxide ions around the Ca and Na ions occupying the M1 through four sites. The M1 and M2 cites create distorted
pentagonal bipyramids while the M3 and M4 create tricapped
trigonal prisms. The M3 and M4
polyhedra share faces when they are next to each other and form columns parallel to [001] while isolated sulfate tetrahedra alternate along the
c axis. ==Physical properties==