Por favor, use este identificador para citar o enlazar a este item:
http://hdl.handle.net/10261/232909
COMPARTIR / EXPORTAR:
SHARE CORE BASE | |
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
Título: | Cyclometalated NHCs Pt(II) compounds with chelating P^P and S^S ligands: From blue to white luminescence |
Autor: | Jaime, Sara; Arnal, Lorenzo CSIC ORCID; Sicilia, Violeta CSIC ORCID; Fuertes, Sara CSIC ORCID | Fecha de publicación: | 2020 | Editor: | ACS Publications | Citación: | Organometallics 39(20): 3695–3704 (2020) | Resumen: | Ionic [Pt(C^C*A/B)(P^P)]PF6 and neutral [Pt(C^C*A/B)(S^S)] complexes were designed and synthesized containing cyclometalated N-heterocyclic carbenes (C^C*A/B) and diphosphines (P^P: dpfppe, dcypm) or dithiocarbamates (S^S: dmdtc, pdtc) as chelating ligands. Their structural and spectroscopic properties were investigated and found to be dependent on both cyclometalated (C^C*A/B) and ancillary (P^P, S^S) ligands. The photophysical and computational studies for the [Pt(C^C*A/B)(P^P)]+complexes disclose the nature of the low-lying electronic transitions to be mainly intraligand charge transfer [ILCT (C^C*A/B)] with some contribution of ligand-to-ligand charge transfer (LL’CT) or ligand-to metal charge transfer (LMCT) for the dpfppe or dcypm derivatives, respectively. The blue and cyan emissions of PMMA films doped with the [Pt(C^C*A/B)(P^P)]+ complexes exhibited very high quantum yields (QYs) reaching up to ∼90%. However, the low-energy absorptions and emissions of the [Pt(C^C*A/B)(S^S)] complexes in solution (rt or 77 K) arise from mixed ILCT [C^C*A/B]/MLCT [dπ(Pt) → π*(C^C*A/B)] excited states, showing no change with the different S^S ligands. In solid-state and in doped films, these dithiocarbamate complexes, excluding 8B, display dual emissions with the high-energy vibronic band (3ILCT /3MLCT) appearing together with an additional low-energy structureless band. The latter is attributed to 3ππ* transitions originated from π-stacked aggregates, as reported in the X-ray structure of 7A. Thus, white light emissions can be obtained with photo- and colorimetric values lying inside the stipulated limits for general lighting applications; yet, they display low QY. | Versión del editor: | https://doi.org/10.1021/acs.organomet.0c00510 | URI: | http://hdl.handle.net/10261/232909 | DOI: | 10.1021/acs.organomet.0c00510 | E-ISSN: | 1520-6041 |
Aparece en las colecciones: | (ISQCH) Artículos |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
---|---|---|---|---|
accesoRestringido.pdf | 59,24 kB | Adobe PDF | Visualizar/Abrir |
CORE Recommender
SCOPUSTM
Citations
10
checked on 21-abr-2024
WEB OF SCIENCETM
Citations
9
checked on 24-feb-2024
Page view(s)
69
checked on 24-abr-2024
Download(s)
16
checked on 24-abr-2024
Google ScholarTM
Check
Altmetric
Altmetric
NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.