Publication: The Synthesis and Complex Formation of Four New Macrocyclicvic-Dioximes
| dc.contributor.author | Karadeniz, K. | |
| dc.contributor.author | Bek[acaron]ròlu, Ö. | |
| dc.date.accessioned | 2026-01-24T23:45:49Z | |
| dc.date.issued | 1983-01-01 | |
| dc.description.abstract | Abstract Four new macrocyclic vic-dioximes, dibenzo[e,k]-2,3-bis(hydroxyimino)-1,4-diaza-7,10-dioxa-2,3,8,9-tetrahydrocyclododecine (ODIH2), dibenzo[e,n]-2,3-bis(hydroxyimino)-1,4-diaza-7,10,13-trioxa-2,3,8,9,11,12-hexahydrocyclopentadecine (OTRH2), dibenzo[e,q]-2,3-bis(hydroxyimino)-1,4-diaza-7,10,13,16-tetraoxa-2,3,8,9,11,12,14,15-octahydrocyclo-octadecine (OTEH2), and dibenzo[e,t]-2,3-bis(hydroxyimino)-1,4-diaza-7,10,13,16,19-pentaoxa-2,3,8,9,11,12,14,15,17,18-decahydrocycloheneicosine (OPTH2) have been synthesized from anti-dichloroglyoxime and the corresponding l,ω-diamines. All these dioximes are in anti-form according to i.r. and H n.m.r. spectral data. The interaction of macrocycles with alkali salts are weak as expected since 2 aza-groups are present. Cu(II), Ni(II), Co(II), Cd(II), Zn(II), and UO2(VI) complexes of four vic-dioximes have been isolated and their structures have been determined by using i.r., u.v.-vis. spectra and elemental analyses. | |
| dc.description.uri | https://doi.org/10.1080/00945718308071336 | |
| dc.description.uri | https://dx.doi.org/10.1080/00945718308071336 | |
| dc.identifier.doi | 10.1080/00945718308071336 | |
| dc.identifier.eissn | 1532-2440 | |
| dc.identifier.endpage | 1045 | |
| dc.identifier.issn | 0094-5714 | |
| dc.identifier.openaire | doi_dedup___::375802f4defe286024a538c7fa8b8026 | |
| dc.identifier.startpage | 1029 | |
| dc.identifier.uri | https://hdl.handle.net/11527/39815 | |
| dc.identifier.volume | 13 | |
| dc.language.iso | eng | |
| dc.publisher | Informa UK Limited | |
| dc.relation.ispartof | Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry | |
| dc.sdg.type | Goal 3: Good Health and Well-being | |
| dc.title | The Synthesis and Complex Formation of Four New Macrocyclicvic-Dioximes | |
| dc.type | Article | |
| dspace.entity.type | Publication |