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Intramolecular π Stacking in Cationic Iridium(III) Complexes with Phenyl-Functionalized Cyclometalated Ligands: Synthesis, Structure, Photophysical Properties, and Theoretical Studies

Li, Peng; Shan, Guo-Gang; Cao, Hong-Tao; Zhu, Dong-Xia; Su, Zhong-Min; Jitchati, Rukkiat; Bryce, Martin R.

Intramolecular π Stacking in Cationic Iridium(III) Complexes with Phenyl-Functionalized Cyclometalated Ligands: Synthesis, Structure, Photophysical Properties, and Theoretical Studies Thumbnail


Authors

Peng Li

Guo-Gang Shan

Hong-Tao Cao

Dong-Xia Zhu

Zhong-Min Su

Rukkiat Jitchati



Abstract

The syntheses of two new heteroleptic cationic iridium complexes containing 2,6-diphenylpyridine (Hdppy) and 2,4,6-triphenylpyridine (Htppy) as the cyclometalated ligands, namely, [Ir(dppy)2phen]PF6 (1, phen = 1,10-phenanthroline) and [Ir(tppy)2phen]PF6 (2), are described. The X-ray crystal structure of 2 reveals a distorted octahedral geometry around the Ir center and close intramolecular face-to-face π–π stacking interactions between the pendant phenyl rings at the 2-position of the cyclometalated ligands and the NN ancillary ligand. This represents a new π–π stacking mode in charged Ir complexes. Complexes 1 and 2 are green photoemitters: their photophysical and electrochemical properties are interpreted with the assistance of density functional theory (DFT) calculations. These calculations also establish that the observed intramolecular interactions cannot effectively prevent the lengthening of the Ir–N bonds of the complexes in their metal-centered (3MC) states. Complexes 1 and 2 do not emit light in light-emitting electrochemical cells (LECs) under conditions in which the model compound [Ir(ppy)2phen]PF6 (3) emits strongly. This is explained by degradation reactions of the 3MC state of 1 and 2 under the applied bias during LEC operation facilitated by the enhanced distortions in the geometry of the complexes. These observations have important implications for the future design of complexes for LEC applications.

Citation

Li, P., Shan, G., Cao, H., Zhu, D., Su, Z., Jitchati, R., & Bryce, M. R. (2014). Intramolecular π Stacking in Cationic Iridium(III) Complexes with Phenyl-Functionalized Cyclometalated Ligands: Synthesis, Structure, Photophysical Properties, and Theoretical Studies. European Journal of Inorganic Chemistry, 2014(14), 2376-2382. https://doi.org/10.1002/ejic.201400007

Journal Article Type Article
Publication Date May 1, 2014
Deposit Date Nov 24, 2014
Publicly Available Date Nov 26, 2014
Journal European Journal of Inorganic Chemistry
Print ISSN 1434-1948
Electronic ISSN 1099-0682
Publisher Wiley-VCH Verlag
Peer Reviewed Peer Reviewed
Volume 2014
Issue 14
Pages 2376-2382
DOI https://doi.org/10.1002/ejic.201400007
Keywords Iridium, Luminescence, Photophysics, Density functional calculations, Light-emitting cells.
Public URL https://durham-repository.worktribe.com/output/1449942

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Accepted Journal Article (428 Kb)
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Copyright Statement
This is the peer reviewed version of the following article: Li, P., Shan, G.-G., Cao, H.-T., Zhu, D.-X., Su, Z.-M., Jitchati, R. and Bryce, M. R. (2014), Intramolecular π Stacking in Cationic Iridium(III) Complexes with Phenyl-Functionalized Cyclometalated Ligands: Synthesis, Structure, Photophysical Properties, and Theoretical Studies. European Journal of Inorganic Chemistry, 2014 (14): 2376-2382, which has been published in final form at http://dx.doi.org/10.1002/ejic.201400007. This article may be used for non-commercial purposes in accordance With Wiley-VCH Terms and Conditions for self-archiving.






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