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Updated: Jan 24, 2026

Determination of the Photoisomerization Quantum Yield of a Hydrazone Photoswitch
Published on: February 7, 2022
Photoswitchable catalysis based on the isomerisation of double bonds
1Stratingh Institute for Chemistry, Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands. b.l.feringa@rug.nl.
Abstract:
Photoswitchable catalysis is a young but rapidly evolving field that offers great potential for non-invasive dynamic control of both activity and selectivity in catalysis. Within this context, the E/Z photoisomerisation of double bonds in molecular switches and motors is one of the most popular tools to control the catalytic activity essentially due to its reversible nature, the large concomitant geometrical changes, and the high tunability of such photochromic entities. This Feature Article summarises the key developments accomplished over the past years through the incorporation of photoswitchable double bonds into the structure of catalytically competent molecules and shows some perspectives on the remaining challenges and possibilities arising from this, yet still somehow immature, exciting area of research.
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When atoms gain or lose electrons to achieve a more stable electron configuration they form ions. Ionic bonds are electrostatic attractions between ions with opposite charges. Ionic compounds are rigid and brittle when solid and may dissociate into their constituent ions in water. Covalent compounds, by contrast, remain intact unless a chemical reaction breaks them.
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