Partially hydrated zeolite Cs,Na−Y (|Cs 51 Na 24 | [Si 117 Al 75 O 384 ]-FAU) was allowed to react with SnI 2 . The crystal structures of fully dehydrated Cs,Na−Y and of the partially hydrated product Sn,I,Cs,Na−Y (|(Na 4 Cs 6 Sn 4 I 6 ) 0.625 Cs 46 Na 21.5 (H 2 O) 26 | [Si 117 Al 75 O 384 ]-FAU) were determined by single-crystal crystallography using synchrotron X-radiation. They were refined in the space group Fd3m, (a = 24.838(2) Å and 24.873(2) Å) with all unique data to the final error indexes R 1 = 0.053 and 0.060 for the 1885 and 1400 reflections for which F o > 4σ(F o ), respectively. Tetrahedrally distorted Sn 4 I 44+ cubes, symmetry 43m (T d ), center 7.9% of the supercages in the zeolite crystal studied. Each is supported there by four Na + ions and six Cs + ions that bridge between its I − ions and oxygen atoms of the zeolite framework. Each Sn 2+ ion bonds to an additional I − ion in the plane of a 12-ring, which in turn bonds to a Sn 2+ ion in a Sn 4 I 4 4+ group in a neighboring supercage. In this way, the Sn 4 I 4 4+ units connect to form a three-dimensional continuum with formula Na 4 Cs 6 Sn 4 I 6 12+ per supercage. Partially hydrated zeolite Sn,I,Cs,Na−Y has a broad luminescence range from 400 to 800 nm. Upon further hydration, the luminescence spectrum evolved, and its color changed from pale yellow to white.