metal-organic compounds
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The title compound, [Ge2(C8H17N2)4O2], crystallizes with imposed twofold symmetry, which allows the monodentate amidinate ligands to be arranged in a cisoid fashion. The independent Ge—O distances within the central Ge2O2 ring, which is essentially planar (r.m.s. deviation = 0.039 Å), are 1.7797 (8) and 1.8568 (8) Å. The germanium centres adopt a distorted trigonal–bipyramidal geometry, being coordinated by the two O atoms and by one bidentate and one monodentate amidinate ligand (three N atoms). One N-isopropyl group is disordered over two positions; these are mutually exclusive because of `collisions' between symmetry-equivalent methyl groups and thus each has 0.5 occupancy.
organic compounds
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In the title salt, C14H13Br3NOS2+·Br−, synthesized by bromination of mesoionic 2-[2-(piperidin-1-yl)-1,3-dithiol-2-ylium-4-yl]phenolate in glacial acetic acid, the dihedral angle between the 1,3-dithiolium ring and the phenolic substituent ring is 45.9 (3)° due to the steric influence of the ortho-Br group on the 1,3-dithiolium ring. The piperidine ring adopts a chair conformation. In the crystal, the cation and anion are linked by an O—HBr hydrogen bond.
organic compounds
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In the racemic title compound, C14H16BrNO3S2, synthesized from the corresponding ω-bromopropiophenone, the dihedral angle between the plane of the phenol group and that of the planar section [maximum deviation = 0.040 (2) Å] of the morpholine-4-carbodithiolate moiety is 76.36 (10)°. A strong intramolecular phenol O—HO hydrogen bond if present in the molecule. In the crystal, only weak C—HS and C—HO interactions are found.
organic compounds
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In the title compound, C14H15BrN2O2S, synthesized by the reaction of the corresponding phenacyl thiocyanate with morpholine, the dihedral angle between the 1,3-thiazole ring and the phenolic substituent ring is 23.46 (10)° as a result of the steric influence of the ortho-methyl group on the thiazole ring. A strong intramolecular phenolic O—HN hydrogen bond is present in the molecule. In the crystal, a weak C—HOphenol hydrogen bond gives rise to chains lying parallel to [20-1]. A short intermolecular BrOmorpholine interaction is also present [3.1338 (19) Å].