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001017960 001__ 1017960 001017960 005__ 20250924040224.0 001017960 0247_ $$2originalID$$acorda_____he::101150311 001017960 0247_ $$2CORDIS$$aG:(EU-Grant)101150311$$d101150311 001017960 0247_ $$2CORDIS$$aG:(EU-Call)HORIZON-MSCA-2023-PF-01$$dHORIZON-MSCA-2023-PF-01 001017960 0247_ $$2doi$$a10.3030/101150311 001017960 035__ $$aG:(EU-Grant)101150311 001017960 150__ $$a Mechanistic Understanding of The Photoexcited Nitroarene-Mediated Olefin Ozonolysis $$y2024-06-03 - 2026-06-02 001017960 372__ $$aHORIZON-MSCA-2023-PF-01$$s2024-06-03$$t2026-06-02 001017960 450__ $$aNOZONE$$wd$$y2024-06-03 - 2026-06-02 001017960 5101_ $$0I:(DE-588b)5098525-5$$aEuropean Union$$bCORDIS 001017960 680__ $$a Photoexcited nitroarenes as ozone surrogates in olefin ozonolysis. Olefins are commonly converted by olefin ozonolysis into synthetic intermediates including aldehydes, ketones and carboxylic acids for the bulk chemical industry. Concerns regarding ozone safety have prohibited use of this reaction by fine chemical sectors including the pharmaceutical and agrochemical industries. Recent demonstration that photoexcited nitroarenes can be used as ozone surrogates for the oxidative cleavage of olefins opens the door to use by the fine chemical industry. With the support of the Marie Skłodowska-Curie Actions programme, the NOZONE project aims to make this possible by characterising the key mechanisms governing reactivity. 001017960 909CO $$ooai:publications.rwth-aachen.de:1017960$$pauthority$$pauthority:GRANT 001017960 909CO $$ooai:publications.rwth-aachen.de:1017960 001017960 980__ $$aG 001017960 980__ $$aAUTHORITY 001017960 980__ $$aCORDIS