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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Unusual Terpyridines as Ligands for Novel Light-Emitting Iridium(iii) Complexes: Synthesis and Characterization

Andreas Winter A , Christoph Ulbricht A , Elisabeth Holder A C , Nikolaus Risch B and Ulrich S. Schubert A D
+ Author Affiliations
- Author Affiliations

A Laboratory of Macromolecular Chemistry and Nanoscience, Eindhoven University of Technology & Dutch Polymer Institute, 5600 MB Eindhoven, The Netherlands.

B Chemistry Department, Faculty of Science, Paderborn University, 33098 Paderborn, Germany.

C Current address: Functional Polymers Group & Institute of Polymer Technology, University of Wuppertal, 42097 Wuppertal, Germany.

D Corresponding author. Email: u.s.schubert@tue.nl

Australian Journal of Chemistry 59(11) 773-782 https://doi.org/10.1071/CH06281
Submitted: 5 August 2006  Accepted: 27 September 2006   Published: 17 November 2006

Abstract

Based on S-shaped terpyridines, a series of yellow, orange, and red-orange light-emitting iridium(iii) complexes has been synthesized. The respective compounds have been prepared by the bridge-splitting method starting from the dimeric precursor complexes [(ppy)2Ir-μ-Cl]2, [(ppy-CHO)2Ir-μ-Cl]2, and [(c6)2Ir-μ-Cl]2. The products have been fully characterized by one- and two-dimensional (1H–1H correlation) NMR spectroscopy, elemental analysis, and MALDI-TOF mass spectrometry revealing the successful coordination of the iridium(iii) centres to the S-shaped terpyridine ligands. Furthermore, the quantitative coordination has been verified by the photophysical and electrochemical properties of the mononuclear iridium(iii) complexes. The photoluminescence spectra have shown strong emissions with maxima between 538 and 600 nm. The study of the optical properties of these novel complexes has indicated that the colour shifts are mainly depending on the nature of the cyclometallating ligands.


Acknowledgments

We thank the Dutch Polymer Institute, the Nederlandse Organisatie voor Wetenschappelijk Onderzoek (through the VICI award to U.S.S.), the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie for financial support of this project. We also thank Michael A. R. Meier, Renzo M. Paulus, and Antje M. J. van den Berg for performing the MALDI-TOF MS, thermogravimetric, and elemental analysis measurements, respectively.


References


[1]   (a) J. Slinker, D. Bernards, P. L. Houston, H. D. Abruña, S. Bernhard, G. G. Malliaras, Chem. Commun. 2003,  2392.
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  open url image1