1-(2-Oxo-3,4-dihydro-2H-1,3-benzoxazin-4-yl)urea monohydrate

The organic molecule in the title hydrate, C9H9N3O3·H2O, was obtained by the condenstation of salicylic aldehyde with urea in acetonitrile. The oxazine ring adopts a slightly distorted sofa conformation, with the N atom deviating from the plane passing through the other atoms of the ring by 0.267 (2) Å. The crystal structure displays inter­molecular N—H⋯O and O—H⋯O hydrogen bonding

Dichloridobis(pyridine-2-thiolato-κ2N,S)tin(IV): a new polymorph

The title compound, [SnCl2(C5H4NS)2], is the product of reaction of 2,2′-dipyridyl disulfide with tin tetrachloride. The SnIV atom adopts a distorted octahedral geometry, with the two bidentate pyridine-2-thiolate ligands forming two planar four-membered chelate rings. The two Sn—Cl, two Sn—N and two Sn—S bonds are in cis, cis and trans configurations, respectively. The crystal grown from acetonitrile represents a new monoclinic polymorph in space group C2/c with the molecule having twofold rotational symmetry, the SnIV atom lying on the twofold axis. The molecular structure of the monoclinic polymorph is very close to that of the triclinic polymorph studied previously in space group P-1, the molecule occupying a general position [Masaki & Matsunami (1976). Bull. Chem. Soc. Jpn, 49, 3274–3279; Masaki et al. (1978). Bull. Chem. Soc. Jpn, 51, 3298–3301]. Apparently, the formation of the two polymorphs is determined by the different systems of intermolecular interactions. In the crystal of the monoclinic polymorph, molecules are bound into ribbons along the c axis by C—H...Cl hydrogen bonds, whereas in the crystal of the triclinic polymorph, molecules form chains along the a axis by attractive S...S interactions. The crystal studied was a pseudo-merohedral twin; the refined BASF value is 0.221 (1)

Dichloridobis(pyridine-2-selenolato-κ2N,Se)tin(IV)

The title compound, [SnCl2(C5H4NSe)2], is the product of a reaction of 2,2′-dipyridyl diselenide with tin tetrachloride. The molecule is located about a twofold rotation axis. The coordination environment of the SnIV atom is a distorted octahedron, with two bidentate 2-pyridineselenolate ligands inclined to each other at an angle of 83.96 (7)°. The two Sn—Cl and two Sn—N bonds are in cis configurations, while the two Sn—Se bonds of 2.5917 (3) Å are in a trans configuration, with an Se—Sn—Se angle of 157.988 (15)°. In the crystal, π–π interactions between the pyridine rings [centroid-to-centroid distance of 3.758 (3) Å] and weak intermolecular C—H...Cl hydrogen bonds link the molecules into chains along the c axis