Synthesis and characterization of polypiridine-based rhenium(I) complexes with pyrazino[2,3-f][1,10]phenanthroline
dc.contributor.author | Díaz Harris, Ramiro | |
dc.contributor.author | Francois, Angelica | |
dc.contributor.author | Leiva, Ana Maria | |
dc.contributor.author | Loeb, Barbara | |
dc.contributor.author | Norambuena, Ester | |
dc.contributor.author | Yanez, Mauricio | |
dc.date | 2006 | |
dc.date.accessioned | 2021-04-30T16:46:56Z | |
dc.date.available | 2021-04-30T16:46:56Z | |
dc.description.abstract | A series of tricarbonyl rhenium(l) complexes of the type Jac-[Re-I(CO)(3)(ppl)(L)](0/+), where ppl is pyrazino[2,3-f] [1,10]phenanthroline, and where L is Cl-, TfO-, 4-(tert-butyl)pyridine ('Bu-py), 4-methoxypyridine (MeO-py), 4,4'-bipyridyl (bpy), or 10-(picolin-4-yl)phenothiazine (pptz), were synthesized and fully characterized. In all complexes, an increment in the electron-acceptor properties of ppl compared to the free ligand was observed. This effect was more significant for pyridine-type ligands, especially for pptz, compared to Cl- or TfO-. The properties of fac-[Re(CO)(3)(PPl)(pptz)]PF6 were compared with those of the analogous compound fac-[Re(CO)(3)(dppz)(pptz)]PF6, where dppz is dipyrido(3,2-a: 2',3'-c)phenazine, the goal being to generate long-lived excited charge-transfer (CT) states. In this respect, fac-[Re(CO)(3)(PPl)(pptz)]PF6 seems to be a promising candidate. | |
dc.identifier.citation | HELVETICA CHIMICA ACTA,Vol.89,1220-1230,2006 | |
dc.identifier.uri | http://repositoriodigital.uct.cl/handle/10925/3407 | |
dc.language.iso | en | |
dc.publisher | WILEY-V C H VERLAG GMBH | |
dc.source | HELVETICA CHIMICA ACTA | |
dc.title | Synthesis and characterization of polypiridine-based rhenium(I) complexes with pyrazino[2,3-f][1,10]phenanthroline | |
dc.type | Article | |
uct.catalogador | WOS | |
uct.indizacion | SCI |