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Structures of substituted di-aryl-1, 3,4-oxadiazole derivatives: 2,5-bis(pyridyl)- and 2,5-bis(aminophenyl)-substitution

  • Crystal structures of four different di-aryl-1,3,4-oxadiazole compounds (aryl = 2-pyridyl-, 3-pyridyl-, 2-aminophenyl-, 3-aminophenyl-) are determined. Crystallization of di(2-pyridyl)-1,3,4-oxadiazole yielded monoclinic and triclinic polymorphs. The structures are characterized by the occurrence of pi-pi interactions. Additionally, in case of the aminophenyl compounds intra- as well as intermolecular hydrogen bonds are found that influence the packing motif as well. Since these molecules are often used as ligands in metal-organic complexes similarities and differences of the molecular conformation between the molecules in the pure crystals and that of the ligands in the complexes are discussed. (c) 2006 Elsevier B.V. All rights reserved.

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Metadaten
Author details:Franziska EmmerlingORCiDGND, Ingo Orgzall, Günter Reck, Burkhard W. Schulz, Sabine Stockhause, Burkhard SchulzORCiDGND
DOI:https://doi.org/10.1016/j.molstruc.2006.03.076
ISSN:0022-2860
Title of parent work (English):Journal of molecular structure
Publisher:Elsevier
Place of publishing:Amsterdam
Publication type:Article
Language:English
Date of first publication:2006/12/04
Publication year:2006
Release date:2020/04/15
Tag:1,3,4-oxadiazole; crystal structure; hydrogen bonds; molecular conformation
Volume:800
Issue:1-3
Number of pages:11
First page:74
Last Page:84
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Physik und Astronomie
DDC classification:5 Naturwissenschaften und Mathematik / 53 Physik / 530 Physik
Peer review:Referiert
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