<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>62(5)</volume><submitter>Menduti L</submitter><pubmed_abstract>Helicenes combine two central themes in chemistry: extended π-conjugation and chirality. Hetero-atom doping preserves both characteristics and allows modulation of the electronic structure of a helicene. Herein, we report the (BO)&lt;sub>2&lt;/sub> -doped tetrathia[7]helicene 1, which was prepared from 2-methoxy-3,3'-bithiophene in four steps. 1 is formally derived by substituting two (Mes)B-O moieties in place of (H)C=C(H) fragments in two benzene rings of the parent tetrathia[7]helicene. X-ray crystallography revealed a dihedral angle of 50.26(9)° between the two terminal thiophene rings. The (P)-/(M)-1 enantiomers were separated by chiral HPLC and are configurationally stable at room temperature. The experimentally determined enantiomerization barrier of 27.4±0.1 kcal mol&lt;sup>-1&lt;/sup> is lowe</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>e202215468</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10107351</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>(BO)&lt;sub>2&lt;/sub> -Doped Tetrathia[7]helicene: A Configurationally Stable Blue Emitter.</pubmed_title><pmcid>PMC10107351</pmcid><pubmed_authors>Manetto S</pubmed_authors><pubmed_authors>Bolte M</pubmed_authors><pubmed_authors>Baldoli C</pubmed_authors><pubmed_authors>Villani C</pubmed_authors><pubmed_authors>Licandro E</pubmed_authors><pubmed_authors>Wagner M</pubmed_authors><pubmed_authors>Longhi G</pubmed_authors><pubmed_authors>Lerner HW</pubmed_authors><pubmed_authors>Menduti L</pubmed_authors></additional><is_claimable>false</is_claimable><name>(BO)&lt;sub>2&lt;/sub> -Doped Tetrathia[7]helicene: A Configurationally Stable Blue Emitter.</name><description>Helicenes combine two central themes in chemistry: extended π-conjugation and chirality. Hetero-atom doping preserves both characteristics and allows modulation of the electronic structure of a helicene. Herein, we report the (BO)&lt;sub>2&lt;/sub> -doped tetrathia[7]helicene 1, which was prepared from 2-methoxy-3,3'-bithiophene in four steps. 1 is formally derived by substituting two (Mes)B-O moieties in place of (H)C=C(H) fragments in two benzene rings of the parent tetrathia[7]helicene. X-ray crystallography revealed a dihedral angle of 50.26(9)° between the two terminal thiophene rings. The (P)-/(M)-1 enantiomers were separated by chiral HPLC and are configurationally stable at room temperature. The experimentally determined enantiomerization barrier of 27.4±0.1 kcal mol&lt;sup>-1&lt;/sup> is lowe</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-07-10T03:08:21.003Z</modification><creation>2025-04-06T11:21:00.432Z</creation></dates><accession>S-EPMC10107351</accession><cross_references><pubmed>36409523</pubmed><doi>10.1002/anie.202215468</doi></cross_references></HashMap>