Related Experiment Video
Updated: Aug 24, 2026

ARL Spectral Fitting as an Application to Augment Spectral Data via Franck-Condon Lineshape Analysis and Color Analysis
Published on: August 19, 2021
Dyads containing iridium(III) bis-terpyridine as photoactive center: synthesis and electron transfer study
Etienne Baranoff1, Isabelle M Dixon, Jean-Paul Collin
1Laboratoire de Chimie Organo-Minérale, UMR 7513 CNRS, Université Louis Pasteur, Institut Le Bel, 4, rue Blaise Pascal, 67070 Strasbourg, France.
Abstract:
A series of Ir(III)-D dyads based on an iridium(III) bis-terpyridine complex as a photoactive center and tertiary amines as donor groups, as well as their individual components, have been designed to generate photoinduced charge separation. Depending on the donor group, a modular approach or a "chemistry-on-the-complex" approach has been used to prepare three different Ir(III)-D dyads. A detailed photophysical study has been performed on one Ir(III)-D dyad in which a triarylamine is linked to the iridium bis-terpyridine complex with an amido-phenyl group used as a spacer. In acetonitrile at room temperature, steady-state and time-resolved methods gave evidence of a photoinduced charge-separated state Ir(-)-D(+) with a lifetime of 70 ps. This relatively short lifetime could be due to the close proximity between the negative charge, likely localized in the bridging terpyridine, and the oxidized donor group.
More Related Videos
09:45Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
06:08Time-resolved Photophysical Characterization of Triplet-harvesting Organic Compounds at an Oxygen-free Environment Using an iCCD Camera
Published on: December 27, 2018
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Thermal and Photochemical Electrocyclic Reactions: Overview
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Cycloaddition Reactions: MO Requirements for Photochemical Activation
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...