Related Experiment Video
Updated: May 13, 2025

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
On the In Silico Evaluation of the Emission Quantum Yield of Cyclometalated Ir(III) Complexes
Iván Soriano-Díaz1, Alicia Omist1, Ilya D Dergachev2
1Institute for Molecular Science (ICMol), Universitat de València, Catedrático José Beltrán 2, Paterna 46980, España.
Abstract:
The in silico determination of the emission quantum yield (Φem) of a cyclometalated Ir(III) complex requires the evaluation of all its possible radiative and nonradiative decays. The task is challenging, particularly when more than one minimum is present on the potential energy surface of the emitting lowest-energy triplet T1, a situation more common than what was previously thought. In the present contribution, we study all possible radiative and nonradiative paths for the two cyclometalated Ir(III) complexes, [Ir(ppy)2(pyim)]+ and [Ir(diFppy)2(dtb-bpy)]+, indeed characterized by T1 minima of both metal-to-ligand charge transfer and ligand-centered nature. Comparing the computed emission quantum yields accounting for all processes and for only those processes in principle more relevant, we aimed at judging the importance of characterizing all decays to provide an accurate estimation of Φem. Evaluating the barrier between emitting T1 and nonradiative 3MC states obtaining the corresponding transition state or approximating the latter using the CI-NEB method, we aimed at judging the importance of performing transition state optimizations. The latter task, due to its intrinsic complexity and poor convergence behavior, is a bottleneck for the characterization of the photophysics of a complex and consequently prevents a more efficient screening of cyclometalated Ir(III) complexes for technological applications.
More Related Videos
Related Concept Videos
Radical Reactivity: Intramolecular vs Intermolecular
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
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.
Thermal and Photochemical Electrocyclic Reactions: Overview

