Taylor, Dominic and Malcomson, Thomas and Zhakeyev, Adilet and Rosair, Georgina M and Paterson, Martin J and Marques-Hueso, Jose and Dalgarno, Scott J and Vilela, Filipe (2023) Regioselective electrophilic aromatic borylation as a method for synthesising sterically hindered benzothiadiazole fluorophores. RSC Advances, 13 (9). pp. 5826-5832. ISSN 2046-2069
Full text not available from this repository.Abstract
Regioselective stepwise phenylation of 4,7-diarylbenzo[ ][1,2,5]thiadiazole fluorophores has been achieved through a facile one-pot, three-step synthetic strategy involving sequential borylation, hydroxydechlorination and Suzuki-Miyaura cross-coupling reactions. Crucial to the selectivity was the use of BCl to regioselectively install a boronic acid group in the -position of only one of the diaryl groups. The subsequent introduction of -phenyl groups through Suzuki-Miyaura cross-coupling gave rise to twisted structures with hindered intramolecular rotation, providing a structural lever with which the fluorophore absorption and emission properties could be adjusted.