2,4,6-Tris(1′-phenylthio-1-ferrocenyl)boroxin
✍ Scribed by Hua, Duy H. ;McGill, James W. ;Robinson, Paul D. ;Meyers, Cal Y.
- Publisher
- International Union of Crystallography
- Year
- 2001
- Tongue
- English
- Weight
- 330 KB
- Volume
- 57
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
Single-crystal X-ray study T = 168 K Mean '(C±C) = 0.006 A Ê R factor = 0.040 wR factor = 0.095 Data-to-parameter ratio = 14.4 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
The title compound, C 12 H 14 F 3 N 3 S, is a biologically active antiimplantation agent. Its crystal structure is stabilized by intermolecular NÐHÁ Á ÁS hydrogen bonds, which form dimers in a head-to-tail arrangement and link them into a polymeric chain.
The title compound, C 15 H 17 NO 2 S, synthesized as an inhibitor for 5-lipoxygenase, comprises the neutral 1,2-diethyl-3hydroxy-6-phenylthiopyridin-4(1H)-one molecule. The H atom of the hydroxy group and the carbonyl O atom form intermolecular hydrogen bonds with another molecule in a head-to-head
In a search for potent fungicidal agents, the title compound, [Fe(C 5 H 5 )(C 17 H 18 N 3 O)], has been synthesized and its singlecrystal structure determined. It has proven that a bulky group, such as ferrocene, close to the triazole ring results in a decreased fungicidal activity.