In the title compound, [Co(C4H7N2O2)Cl2(C4H8N2O2)], the CoIII ion has a distorted octa­hedral coordination environment. The equatorial plane consists of four N atoms, two each from the dimethyl­glyoxime and dimethyl­glyoximate ligands, while the two axial positions are occupied by two chloride ions. Strong intra­molecular O—H⋯O hydrogen bonds are observed between the dimethyl­glyoxime and dimethyl­glyoximate ligands. Mol­ecules are linked into a chain running along the [101] direction by O—H⋯O and C—H⋯Cl hydrogen bonds. The chains are cross-linked through inter­molecular C—H⋯Cl hydrogen bonds.

The mol­ecule of the title chalcone derivative, C21H20O5, consists of two substituted aromatic rings bridged by a prop-2-en-1-one group. The dihedral angle between the two benzene rings is 28.7 (7)°. In the crystal, mol­ecules are linked into C(10) chains running along the a axis by inter­molecular C—H⋯O hydrogen bonds, and the chains are cross-linked via C—H⋯π inter­actions.

Mol­ecules of the title compound, C22H20N2O2, are situated on crystallographic centres of symmetry. The oxazinane ring adopts a sofa conformation. Mol­ecules are linked into cyclic centrosymmetric dimers via C—H⋯O hydrogen bonds with the motif R 2 2(6). In addition to the C—H⋯O inter­actions, the crystal structure is also stabilized by C—H⋯π inter­actions.

In the title compounds, C22H20N2O4S, (I), and C22H19ClN2O4S, (II), the pyrrolidine rings have twist conformations on the spiro–spiro C—C bonds. In (I), the five-membered ring of the oxindole moiety has an envelope conformation with the spiro C atom as the flap, while in (II) this ring is flat (r.m.s. deviation = 0.042 Å). The mean planes of the pyrrolidine rings are inclined to the mean planes of the indole units [r.m.s deviations = 0.073 and 0.069 Å for (I) and (II), respectively] and the benzothiophene ring systems (r.m.s. deviations = 0.019 and 0.034 Å for (I) and (II), respectively) by 79.57 (8) and 88.61 (7)° for (I), and by 81.99 (10) and 88.79 (10)° for (II). In both compounds, the ethoxycarbonyl group occupies an equatorial position with an extended conformation. The overall conformation of the two molecules differs in the angle of inclination of the indole unit with respect to the benzothiophene ring system, with a dihedral angle between the planes of 71.59 (5) in (I) and 82.27 (7)° in (II). In the crystal of (I), molecules are linkedviapairs of N—H...O hydrogen bonds, forming inversion dimers enclosingR22(14) loops. The dimers are linkedviaC—H...O and bifurcated C—H...O(O) hydrogen bonds, forming sheets lying parallel to (100). In the crystal of (II), molecules are again linkedviapairs of N—H...O hydrogen bonds, forming inversion dimers but enclosing smallerR22(8) loops. Here, the dimers are linked by C—H...O hydrogen bonds, forming ribbons propagating along [010].

In the title compound, C22H21N3O4, the central pyrrolidine ring adopts an envelope conformation with the N atom in the flap position. The indoline ring systems are almost perpendic­ular to the mean plane of the pyrrolidine ring, making dihedral angles of 86.4 (8) and 83.1 (8)°. The acetate group attached to the pyrrolidine ring assumes an extended conformation. In thecrystal, N—H⋯O hydrogen bonds result in the formation of a C(7) chain running along [100]. The crystal packing also features π–π inter­actions [centroid–centroid distance = 3.2032 (11) Å].