Publication:
Strongly luminescent Pt(IV) complexes with a Mesoionic N-Heterocyclic Carbene Ligand: tuning their photophysical properties.

Loading...
Thumbnail Image
Date
2021-02-09
relationships.isAuthorOfPublication
relationships.isSecondaryAuthorOf
relationships.isDirectorOf
Authors
Vivancos Ureña, Ángela ; Jiménez García, Adrián ; Bautista, Delia ; González Herrero, Pablo
item.page.secondaryauthor
item.page.director
Publisher
publication.page.editor
publication.page.department
DOI
https://doi.org/10.1021/acs.inorgchem.1c00410
item.page.type
info:eu-repo/semantics/article
Description
Abstract
The synthesis, electrochemistry, and photophysical properties of a series of bis-cyclometalated Pt(IV) complexes that combine the mesoionic aryl-NHC ligand 4-butyl-3-methyl-1-phenyl-1H-1,2,3-triazol-5-ylidene (trz) with either 1-phenylpyrazole or 2-arylpyridine (C∧N) are reported. The complexes (OC-6-54)-[PtCl2(C∧N)(trz)] bearing cyclometalating 2-arylpyridines present phosphorescent emissions in the blue to yellow color range, which essentially arise from 3LC(C∧N) states, and reach quantum yields of ca. 0.3 in fluid solutions and almost unity in poly(methyl methacrylate) (PMMA) matrices at 298 K, thus representing a class of strong emitters with tunable properties. A systematic comparison with the homologous C2-symmetrical species (OC-6-33)-[PtCl2(C∧N)2], which contains two equal 2-arylpyridine ligands, shows that the introduction of a trz ligand leads to significantly lower nonradiative decay rates and higher quantum efficiencies. Computational calculations substantiate the effect of the carbene ligand, which raises the energy of dσ* orbitals in these derivatives and results in the higher energies of nonemissive deactivating 3LMCT states. In contrast, the isomers (OC-6-42)-[PtCl2(C∧N)(trz)] are not luminescent because they present a 3LMCT state as the lowest triplet.
Citation
item.page.embargo
Collections