Related Experiment Video
Updated: May 24, 2026

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds
Published on: October 18, 2018
Light-induced dynamics in conjugated bis(terpyridine) ligands--a case study toward photoactive coordination polymers
Ronald Siebert1, Andreas Winter, Michael Schmitt
1Institute for Physical Chemistry (IPC), Friedrich Schiller University of Jena, Helmholtzweg 4, 07743 Jena, Germany.
Abstract:
Terpyridine coordination compounds have recently revealed their potential toward optoelectronic applications, which are based on (i) their excellent charge-transfer properties or (ii) intriguing luminescence properties of the systems, depending on their design. This article features recent work in dissecting the photophysical properties of such materials by investigating the photoinduced processes in individual molecular fragments. The article starts considering the terpyridine ligands themselves before discussing the impact of metal coordination. After shedding light into the interplay of different electronic states in the terpyridine complexes, first results of a single-molecule fluorescence study are presented, which allow for correlation of the overall luminescence properties with the structure of the polymer.
More Related Videos
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Thermal and Photochemical Electrocyclic Reactions: Overview
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
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.
UV–Vis Spectroscopy of Conjugated Systems
One of the factors influencing λmax is the extent of conjugation in the...

