# Multistate Azobenzene–Norbornadiene Photoswitches for Molecular Solar Thermal Energy Storage

**Authors:** Glib Arago, Karl‐Heinz Glüsenkamp, Gebhard Haberhauer

PMC · DOI: 10.1002/chem.202502520 · Chemistry (Weinheim an Der Bergstrasse, Germany) · 2025-12-08

## TL;DR

This paper introduces a new type of photoswitch combining azobenzene and norbornadiene to improve solar thermal energy storage by extending energy retention and enabling controlled energy release.

## Contribution

The novel contribution is the development of bi- and trimodal photoswitches with synergistic effects for enhanced molecular solar thermal energy storage.

## Key findings

- Hybrid AZO-NBD photoswitches can be selectively switched to produce all isomer types.
- AZO integration extended NBD half-lives up to 122 days in some cases.
- TFA catalyzed the back-conversion of the metastable isomers.

## Abstract

The combination of two photochromic molecules into a multimodal photoswitch offers the potential to generate new properties related to molecular solar thermal (MOST) systems. A system can only be considered suitable for MOST applications if it meets key criteria, including a high quantum yield and an extended half‐life of the high‐energy isomer. Achieving this combination remains a significant challenge. In this study, we present the coupling of an azobenzene unit (AZO) with a norbornadiene system (NBD) via ester functions to develop new bi‐ and trimodal AZO‐NBD photoswitches that exhibit synergistic effects. Photochemical studies reveal that both the NBD and AZO components of the hybrid are switchable. In one case, all isomer types could be selectively produced. Furthermore, each metastable unit can be switched back independently to its corresponding thermodynamically stable form. The quantum yields and half‐lives for the NBD and AZO components of the hybrid system could be determined separately. The integration of AZOs has demonstrated the potential to extend the half‐lives of NBDs to up to 122 days in certain cases, as confirmed through comparative analysis with reference systems. The enhanced rate of back‐conversion was further facilitated by the presence of TFA as a catalyst.

Systems consisting of two different photoswitches (azobenzene and norbornadiene) are presented, which can be switched by light, store energy, and release it again. The combination of the switching units leads to synergistic effects.

## Linked entities

- **Chemicals:** azobenzene (PubChem CID 2272), norbornadiene (PubChem CID 8473), TFA (PubChem CID 6422)

## Full-text entities

- **Chemicals:** azobenzene (MESH:C009850), AZOs (-), norbornadiene (MESH:C048294), ester (MESH:D004952), TFA (MESH:D014269)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12790303/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12790303/full.md

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Source: https://tomesphere.com/paper/PMC12790303