ABSTRACT
The syntheses and crystal structures of 2,3-bis-[3-(tri-fluoro-meth-yl)phen-yl]-2,3-di-hydro-4H-1,3-benzo-thia-zin-4-one (di-m-CF3; C22H13F6NOS) (1) and 2,3-bis-(4-methyl-phen-yl)-2,3-di-hydro-4H-1,3-benzo-thia-zin-4-one (di-p-CH3; C22H19NOS) (2) are reported. Each structure is racemic: the asymmetric unit of 2 consists of two mol-ecules. In both 1 and 2, the six-membered 1,3-thia-zine ring is close to an envelope conformation with the chiral C atom forming the flap. In 1, the 2-aryl group is pseudo-equatorial, while in 2 it is pseudo-axial. In 1, the pendant aryl rings form a V shape with an inter-centroid distance of 3.938â (3)â Å and an acute dihedral angle of 48.3â (2)° between them. Both CF3 groups are disordered over two orientations in 0.687â (19):0.313â (19) and 0.667â (16):0.33â (16) ratios. In each of the independent mol-ecules of 2, the aryl rings are almost orthogonal to each other [dihedral angles = 85.50â (12) and 86.07â (11)°]. In both structures, the chiral C atom and the O atoms participate in C-Hâ¯O-type hydrogen bonding between symmetry-related mol-ecules of 1 or the independent enanti-omers in 2, forming chains along the c-axis direction in 1 and the b-axis direction in 2. Additionally, in 1, π-π contacts of both face-to-face and edge-to-face type, as well as π-Hâ¯O and π-Hâ¯F inter-actions are observed. In 2, a racemic mixture of mol-ecules forms layers in the ac plane linked by weak π-π and C-Hâ¯π inter-actions.