Synthesis and complexes of the sexidentate macrocycle 15-methyl-1,4,7,10,13-pentaazacyclohexadecan-15-amine

Citation
Pv. Bernhardt et al., Synthesis and complexes of the sexidentate macrocycle 15-methyl-1,4,7,10,13-pentaazacyclohexadecan-15-amine, INORG CHIM, 300, 2000, pp. 604-612
Citations number
39
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANICA CHIMICA ACTA
ISSN journal
00201693 → ACNP
Volume
300
Year of publication
2000
Pages
604 - 612
Database
ISI
SICI code
0020-1693(20000430)300:<604:SACOTS>2.0.ZU;2-R
Abstract
The potentially sexidentate polyamine macrocycle 15-methyl-1,4,7,10,13-pent aazacyclohexadecan-15-amine (1) was prepared via a copper(II)-templated rou te from 3,6,9-triazaundecan-1,ll-diamine, formaldehyde and nitroethane whic h first formed the copper(II) complex of the macrocycle 15-methyl-15-nitro- 1,4,7,10,13-pentaazacyclohexadecane (2), reduced subsequently with zinc and aqueous acid to yield 1. The hexaamine 1, with five secondary amine groups in the macrocyclic ring and one pendant primary amine group, forms inert s exidentate octahedral complexes with cobalt(III), chromium(III) and iron(II I). An X-ray structure of [Co(1)](ClO4)(3) defines the distorted octahedron of the complex cation and shows it is a symmetrical isomer with all nitrog ens bound and the central aza group trans to the pendant primary amine grou p. The [M(1)](3+) ions are all stable indefinitely in aqueous solution and exhibit spectra consistent with MN6 d(3) (Cr), low-spin d(5) (Fe) and low-s pin d(6) (Co) electronic ground states. For each complex, a reversible M(II I/II) redox couple is observed. (C) 2000 Elsevier Science S.A. All rights r eserved.