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The crystal structure of the title compound, [Ti(C11H19NSi)Cl2], has been determined as part of a broad investigation of half-sandwich titanium complexes. Titanium has a pseudo-tetrahedral coordination formed by two Cl atoms [Ti—Cl = 2.2719 (4) and 2.2730 (4) Å], the N atom of the N-tert-butyl group [Ti—N = 1.9094 (12) Å] and the silyl-substituted Cp ligand [metal–Cp ring centroid distance = 2.0185 (9) Å]. The tert-butyl group was found to be disordered.

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Single crystals of the LaMg2 cubic Laves phase were synthesized by arc melting. The binary LaMg2 compound has been shown to adopt the MgCu2-type structure. The coordination sphere of the rare earth metal, adopting a site symmetry of \overline{1}, consists only of 12 Mg atoms. The site symmetry of the alkaline earth metal is \overline{3}m, giving rise to superimposed distorted MgLa6 and MgMg6 octa­hedra.

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(NH4)2[Co(H2O)6]3(HPO3)4 is a member of the isotypic (NH4)2[T(H2O)6]3(HPO3)4 family, where T = Co, Ni or Mg. The structure of (NH4)2[Co(H2O)6]3(HPO3)4 is composed of the units [Co(H2O)6]2+, (HPO3)2- and NH4+, which inter­act via an intricate network of hydrogen bonds. One of the Co atoms is located at a site of 2/m symmetry, whereas the other central atoms, viz. the second Co, the two P and ammonium N atom, are located at sites of m symmetry.

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(NH4)2[Ni(H2O)6]3(HPO3)4 is a member of the isotypic (NH4)2[T(H2O)6]3(HPO3)4 family, where T = Co, Ni or Mg. The structure of (NH4)2[Ni(H2O)6]3(HPO3)4 is composed of the units [Ni(H2O)6]2+, (HPO3)2- and NH4+, which inter­act via an intricate network of hydrogen bonds. One of the Ni atoms is located at a site of 2/m symmetry, whereas the other central atoms, viz. the second Ni, the two P and ammonium N atom, are located at sites of m symmetry.
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