0 Datasets
0 Files
Get instant academic access to this publication’s datasets.
Yes. After verification, you can browse and download datasets at no cost. Some premium assets may require author approval.
Files are stored on encrypted storage. Access is restricted to verified users and all downloads are logged.
Yes, message the author after sign-up to request supplementary files or replication code.
Join 50,000+ researchers worldwide. Get instant access to peer-reviewed datasets, advanced analytics, and global collaboration tools.
✓ Immediate verification • ✓ Free institutional access • ✓ Global collaborationJoin our academic network to download verified datasets and collaborate with researchers worldwide.
Get Free AccessWe report on the synthesis and characterization of bis-cyclometalated iridium(III) complexes with 4-phenyl-1H-[1,2,3]triazole, synthesized via a “click”-chemistry approach, as a new type of cyclometalating ligand. The photophysical and electrochemical properties of these complexes are investigated experimentally as well as theoretically by using density functional theory. The properties of these new complexes are compared to their known 2-phenylpyridinato analogues. The emission of the herein described complexes is clearly influenced by the applied ancillary ligand and can be adjusted over a broad range of frequencies. The results indicate that the phenyl-1H-[1,2,3]triazole ligands in general cause a spectral blue shift.
Beatrice Beyer, Christoph Ulbricht, Daniel Escudero, Christian Friebe, Andreas Winter, Leticia González, Ulrich Sigmar Schubert (2009). Phenyl-1<i>H</i>-[1,2,3]triazoles as New Cyclometalating Ligands for Iridium(III) Complexes. , 28(18), DOI: https://doi.org/10.1021/om9003785.
Datasets shared by verified academics with rich metadata and previews.
Authors choose access levels; downloads are logged for transparency.
Students and faculty get instant access after verification.
Type
Article
Year
2009
Authors
7
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1021/om9003785
Access datasets from 50,000+ researchers worldwide with institutional verification.
Get Free Access