Arsenic(III) oxide intercalate with ammonium chloride: crystal structure revision and thermal characterization.

According to the crystal structure determination by Edstrand & Blomqvist [Ark. Kemi (1955), 8, 245-256], intercalate NH 4 Cl·As 2 O 3 ·0.5H 2 O ({\bf Y_{{NH}_{4}Cl}}) is not isostructural with compound KCl·As 2 O 3 ·0.5H 2 O. This is very unlikely because both NH 4 Br·2As 2 O 3 and KBr·2As 2 O 3 as well as NH 4 I·2As 2 O 3 and KI·2As 2 O 3 are isostructural. Hence, intercalate {\bf Y_{{NH}_{4}Cl}} has been studied using single-crystal X-ray diffraction in addition to attenuated total reflection Fourier transform infrared (ATR-FTIR) and 15 N solid-state magic-angle spinning nuclear magnetic resonance (ssNMR) spectroscopies. These techniques indicate that revising the previous crystal structure model is necessary. Compound {\bf Y_{{NH}_{4}Cl}} crystallizes in space group P6/mmm with unit-cell parameters a = 5.25420 (10) Å and c = 12.6308 (3) Å and is isostructural with KCl·As 2 O 3 ·0.5H 2 O. The presence of two symmetry-independent ammonium cations in the structure has been unequivocally confirmed using 15 N ssNMR spectroscopy. The 15 N ssNMR spectrum of intercalate {\bf Y_{{NH}_{4}Cl}} has been compared with analogous spectra of NH 4 Br·2As 2 O 3 and NH 4 I·2As 2 O 3 which allowed for a probable assignment of signals to ammonium cations occupying particular sites in the crystal structures. Thermogravimetry, differential scanning calorimetry and variable-temperature ATR-FTIR spectra have revealed that intercalate {\bf Y_{{NH}_{4}Cl}} is dehydrated between 320 and 475 K. Upon cooling or standing in moist air water is re-absorbed. Dehydration leads to significant shortening of the c unit-cell parameter as revealed by powder X-ray diffraction [c = 12.1552 (7) Å at 293 K]. Compound {\bf Y_{{NH}_{4}Cl}} decomposes on prolonged heating above 490 K to arsenic(III) oxide and ammonium chloride.