http://www.cnr.it/ontology/cnr/individuo/prodotto/ID51103
Diastereoselective Formation of Chiral Tris-Cyclometalated Iridium(III) Complexes: Characterization and Photophysical Properties (Articolo in rivista)
- Type
- Label
- Diastereoselective Formation of Chiral Tris-Cyclometalated Iridium(III) Complexes: Characterization and Photophysical Properties (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ja048655d (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- C. Shaffner-Hamann; A. von Zelewsky; A. Barbieri; F. Barigelletti; G. Muller; J. Riehl; A. Neels (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- 1. Univ Fribourg, Dept Chem, CH-1700 Fribourg, Switzerland
2. CNR, Ist ISOF, I-40129 Bologna, Italy
3. Univ Minnesota, Dept Chem, Duluth, MN 55812 USA
4. Univ Neuchatel, Inst Chem, CH-2000 Neuchatel, Switzerland (literal)
- Titolo
- Diastereoselective Formation of Chiral Tris-Cyclometalated Iridium(III) Complexes: Characterization and Photophysical Properties (literal)
- Abstract
- Chiral, facial tris-cyclometalated Ir(III) complexes, fac-Delta-Ir(pppy)(3), fac-Lambda-Ir(pppy)(3), fac-Lambda-IrL (where pppy is (8R,10R)-2-(2'-phenyl)-4,5-pinenopyridine and L is a tripodal ligand comprising three pppy moieties connected through a mesityl spacer) have been synthesized and characterized. In IrL, NMR and CD studies indicate that only one diastereomer is formed, with the A configuration at the metal center, whereas enantiopure pppy yields the fac-Lambda- and the fac-Delta-stereoisomer in a ratio 2:3. fac-Lambda-IrL was structurally characterized using X-ray crystallography. The luminescence properties including CPL, of the three complexes and their sensitivity to dioxygen were examined. (literal)
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- Autore CNR
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