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Article type: Research Article
Authors: Dopke, Joel A. | Hugdahl, Jeffrey D. | Klausmeyer, Kevin K. | Brill, Matthew P. | Jaremkoĩ, Daniel S.
Affiliations: Alma College, Department of Chemistry, Alma, MI, USA | Department of Chemistry, Mercer University, Macon, GA, USA | Department of Chemistry and Biochemistry, Baylor University, Waco, TX, USA
Note: [] Corresponding author: Joel A. Dopke, Department of Chemistry, Alma College, Alma, MI 48801, USA. Tel.: +1 989 463 7395; Fax: +1 989 463 7076; E-mail: [email protected]
Abstract: The heterocycle 1-aza-4-oxa-7-thiacyclononane ([9]aneNOS, 5) was prepared from the intermediate N-p-toluenesulfonyl-1-aza-4-oxa-7-thiacyclononane (3) upon its deprotection via Na/Hg amalgam. The byproduct, N,N′-bis-(p-tolylsulfonyl)-1,13-diaza-7,16-dioxa-4,10-dithiacylododecane (4), was also isolated from the pot mixture of 3. Compound 5 was characterized by 1H and 13C NMR, and IR spectroscopy. Compounds 3 and 4 were characterized by 1H and 13C NMR, and IR spectroscopy, elemental analysis, and X-ray crystallography. The reaction of 5 with Ni(BF4)2·6 H2O in methanol produced the sandwich complex ([9]aneNOS)2Ni(BF4)2, 6, which was characterized by UV-visible and IR spectroscopy, elemental analysis, and X-ray crystallography.
Keywords: Heterocycle, azacrown, thioether, cyclononane
DOI: 10.3233/MGC-2011-0045
Journal: Main Group Chemistry, vol. 10, no. 2, pp. 153-163, 2011
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