Di-l-acetato-bis[l-2-hydroxy-N,N 0 0 0 -bis(2-oxidobenzyl)propane-1,3-diamine]bis(N,N 0 0 0 -dimethylformamide)trinickel(II) N,N 0 0 0 -dimethylformamide disolvate
Bis[μ-2-hydroxy-N′-(4-hydroxy-2-oxidobenzylidene)benzohydrazide]bis[pyridinezinc(II)] dimethylformamide disolvate
✍ Scribed by Huang, Jin-Shang ;Li, Ming-Tian
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 885 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
Reaction of 2,4-dihydroxybenzaldehye salicylhydrazide (L) with Zn(OAc) 2 Á2H 2 O in a mixed solvent of pyridine and N,Ndimethylformamide (DMF) resulted in the formation of the title complex, [Zn 2 (C 14 H 10 N 2 O 4 ) 2 (C 5 H 5 N) 2 ]Á2C 3 H 7 NO. The asymmetric unit contains one complete neutral zinc complex and one-half of a second complex with crystallographic inversion symmetry, together with three DMF solvent molecules. The Zn atoms, all having the same coordination geometry, are coordinated by three O atoms and two N atoms in a distorted tetragonal-pyramidal geometry, with phenolate O atoms acting as bridges between the Zn atoms.
Symmetry code: (i) Àx; Ày þ 2; Àz þ 2.
Table 2
Hydrogen-bond geometry (A ˚, ).
📜 SIMILAR VOLUMES
In the title compound, [Zn 2 (C 14 H 8 N 2 O 4 )(C 2 H 8 N 2 ) 2 ]Á2C 3 H 7- NOÁ2H 2 O, the Zn 2 complex molecule lies on a crystallographic inversion centre. The two Zn atoms are bridged by two diazine N atoms of a 1,2-bis(salicyloyl)hydrazine(4À) ligand (bsh 4À ); the inversion centre is located a
In the original paper by Qiu, Yang, Liu & Zhu [__Acta Cryst.__ (2006), E**62**, m1320–m1231], the H atoms attached to N1 and N3 are positioned incorrectly. These have been deleted and the structure rerefined. The correct name of the structure is bis(2,4-dichlorobenzaldehyde 2-hydroxybenzoylhydrazona
Single-crystal X-ray study T = 298 K Mean '(C±C) = 0.006 A Ê R factor = 0.039 wR factor = 0.118 Data-to-parameter ratio = 11.9 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.