Ultrafast transient IR spectroscopy and DFT calculations of ruthenium(ii) polypyridyl complexes
Author:
Affiliation:
1. Département de Chimie Physique
2. Université de Genève
3. 1211 Genève
4. Switzerland
Abstract
TRIR spectroscopy identifies the low-energy ligand-field state in the relaxation cascade for ruthenium(ii) polypyridyl complexes.
Funder
Swiss National Science Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/SC/C6SC01220E
Reference51 articles.
1. Mechanism of Ligand Photodissociation in Photoactivable [Ru(bpy)2L2]2+ Complexes: A Density Functional Theory Study
2. Ru(II) dyads derived from α-oligothiophenes: A new class of potent and versatile photosensitizers for PDT
3. Computational Study of the Lowest Triplet State of Ruthenium Polypyridyl Complexes Used in Artificial Photosynthesis
4. New Ru(II) Complexes for Dual Photoreactivity: Ligand Exchange and 1O2 Generation
5. Combination of Ru(ii) complexes and light: new frontiers in cancer therapy
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