## Abstract The condensation of malonoaldehyde derivatives with either a 3‐amino‐[1,2,4]‐triazole or a 3,5‐diamino‐[1,2,4]‐triazole precursor was studied. In agreement with previous reports, two different bicycles, namely, bearing the regioisomeric [1,2,4]triazolo[1,5‐a]pyrimidine (**1**) or[1,2,4]
A Nonanuclear NiII Cluster with a 1,2,4-Triazolo[4,3-a]pyrimidine Derivative
✍ Scribed by Sawsan Salameh; Mohammad Abul-Haj; Miguel Quirós; Juan M. Salas
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 87 KB
- Volume
- 2005
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
Abstract
This article describes the nickel cluster compound Ni~9~L~8~(OH)~6~(NH~3~)~4~(H~2~O)~8~~4~·8H~2~O, where L represents the anionic form of the ligand 7,8‐dihydro‐1,2,4‐triazolo[4,3‐a]pyrimidin‐7‐one. The structure of the cation of this compound is rather complicated, involving nine metal atoms, eight bridging organic ligands, bridging hydroxyl groups, and terminal ammonia and water molecules. The central nickel atom lies on a crystallographic inversion centre, while the other eight define two disorted “cubane‐like” [Ni~4~(OH)~3~]^5+^ subclusters. Each subcluster is linked to the central atom by three triple bridging organic ligands. Additional L ligands bridge two external metal atoms in each subcluster. The variation with temperature of the magnetic susceptibility of the compound indicates the presence of both ferromagnetic and antiferromagnetic interactions; the latter is predominant. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)
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The cation of the title molecule, C~5~H~5~N~4~ ^+^·Cl^−^, is strictly planar; it occupies a special position on a mirror plane. The protonation of the heterocycle takes place, as expected, at an N atom of the imidazole ring. This H atom is hydrogen bonded to the chloride anion.
This article covers all the research work published until September 1998 about the coordination chemistry of 1,2,4-triazolo-[1,5-a]pyrimidine derivatives. The revision is mainly focused in the structural features of the compounds, obtained from single crystal X-ray diffraction. The references are cl