biostudies-literatureSalthouse RJEuropean Innovation CouncilEuropean Research CouncilEuropean Commission's Horizon 2020 Framework Programe16629https://www.ebi.ac.uk/biostudies/studies/S-EPMC12759240biostudies-literatureUnknown65(1)The norbornadiene/quadricyclane (NBD/QC) photoswitch pair is a promising system for molecular solar thermal (MOST) energy storage. Multichromophoric systems with two or more photoswitches can offer red-shifted absorption, higher energy densities, and additional functionality. Here, a series of ortho- and para-substituted NBD dimers bearing methoxy, hexoxy (for solubility), and cyano groups were synthesised and evaluated for their MOST properties. Compared to monomers, the dimers display red-shifted absorption and improved solar spectrum match, with onsets between 448-488 nm, owing to their donor-acceptor design and extended conjugation. A key finding is the tunable relationship between molecular structure, photoluminescence and photoisomerisation: para-dimers exhibit efficient fluorescence, whilst ortho-dimers are superior photoswitches with quantum yields of isomerisation, Φ_i, up to 63%. Solvent choice further modulates behaviour; Φ_i is higher in acetonitrile, whereas fluorescence is more efficient in toluene. This interplay allows tailoring for specific functions. The best-performing photoswitches were studied in a liquid-chip device, achieving a record solar conversion efficiency of 2.9%. Catalytic back-conversion using cobalt phthalocyanine on carbon and macroscopic heat release experiments at 0.1 M yielded a 5.78 °C temperature increase. This first experimental macroscopic heat release of a dimeric system provides important insights into design challenges and opportunities for advancing multichromophoric systems towards MOST applications.Angewandte Chemie (International ed. in English)Modulation of Photoluminescence and Solar Thermal Energy Storage in Norbornadiene-Quadricyclane Dimers.PMC12759240101046364951801101002131Fernandez LEtherington MKElholm JLFerreira PSalthouse RJMoth-Poulsen KCortellazzi IHolzel HfalseModulation of Photoluminescence and Solar Thermal Energy Storage in Norbornadiene-Quadricyclane Dimers.The norbornadiene/quadricyclane (NBD/QC) photoswitch pair is a promising system for molecular solar thermal (MOST) energy storage. Multichromophoric systems with two or more photoswitches can offer red-shifted absorption, higher energy densities, and additional functionality. Here, a series of ortho- and para-substituted NBD dimers bearing methoxy, hexoxy (for solubility), and cyano groups were synthesised and evaluated for their MOST properties. Compared to monomers, the dimers display red-shifted absorption and improved solar spectrum match, with onsets between 448-488 nm, owing to their donor-acceptor design and extended conjugation. A key finding is the tunable relationship between molecular structure, photoluminescence and photoisomerisation: para-dimers exhibit efficient fluorescence, whilst ortho-dimers are superior photoswitches with quantum yields of isomerisation, Φ_i, up to 63%. Solvent choice further modulates behaviour; Φ_i is higher in acetonitrile, whereas fluorescence is more efficient in toluene. This interplay allows tailoring for specific functions. The best-performing photoswitches were studied in a liquid-chip device, achieving a record solar conversion efficiency of 2.9%. Catalytic back-conversion using cobalt phthalocyanine on carbon and macroscopic heat release experiments at 0.1 M yielded a 5.78 °C temperature increase. This first experimental macroscopic heat release of a dimeric system provides important insights into design challenges and opportunities for advancing multichromophoric systems towards MOST applications.2026-01-01T00:00:00Z2026 Jan2026-06-06T09:44:29.247Z2026-05-28T03:12:15.668ZS-EPMC127592404118939710.1002/anie.202516629