Structural and IR-Spectroscopic Characterization of Aqua Lithium Acesulfamate, an Outlier of the M(ace), M: Na+, K+, Rb+, Cs+, Isomorphic Series

PIRO, OSCAR E.; ECHEVERRÍA, GUSTAVO A.; PARAJÓN-COSTA, BEATRIZ S.; BARAN, ENRIQUE J.

JOURNAL OF CHEMICAL CRYSTALLOGRAPHY

SPRINGER/PLENUM PUBLISHERS

Año: 2017 vol. 47 p. 226 - 232

1074-1542

Abstract: The crystal structure of aqua lithium 6-methyl-1,2,3,-oxathiazine-4(3H)-one, 2.2-dioxide, for short Li(ace)H2O, was determined by X-ray diffraction methods. It crystallizes in the triclinic P1 ¯ space group with a = 6.1750(9) Å, b = 7.3969(9) Å, c = 9.016(1) Å, α = 105.88(1)°, β = 94.59(1)°, γ = 97.80(1)°, and Z = 2 molecules per unit cell. The crystal structure of Li(ace)H2O sharply departs from the other heavier alkaline-metal acesulfamates, namely the monoclinic isotypic M-ace (M from Na+ to Cs+) family of salts. Lithium is in a distorted LiO4 tetrahedral coordination with acesulfamate carbonyl, sulfoxide and water oxygen atoms. The FTIR spectrum of the new compound was also recorded and is briefly discussed. Some comparisons with other simple acesulfamate salts are also made. Graphical Abstract: The synthesis of aqua lithium acesulfamate, Li(C4H4NO4S)H2O, and its structural characterization by single-crystal X-ray diffractometry are reported. The FTIR spectrum of the salt is analyzed by comparison with data of related compounds. [Figure not available: see fulltext.].