Intramolecular Borylation via Sequential B‐Mes Bond Cleavage for the Divergent Synthesis of B,N,B‐doped Benzo[4]helicenes
| dc.contributor.author | Knoeller, Julius | en |
| dc.contributor.author | Meng, Guoyun | en |
| dc.contributor.author | Wang, Xiang | en |
| dc.contributor.author | Hall, David | en |
| dc.contributor.author | Pershin, Anton | en |
| dc.contributor.author | Beljonne, David | en |
| dc.contributor.author | Olivier, Yoann | en |
| dc.contributor.author | Laschat, Sabine | en |
| dc.contributor.author | Zysman-Colman, Eli | en |
| dc.contributor.author | Wang, Suning | en |
| dc.date.accessioned | 2020-01-03T19:46:04Z | |
| dc.date.available | 2020-01-03T19:46:04Z | |
| dc.date.issued | 2019 | |
| dc.description.abstract | New symmetric and unsymmetric B,N,B‐doped benzo[4]helicenes 3 ‐ 6a/b have been achieved in good yields, using a three‐step process, starting from N(tolyl) 3 in a highly divergent manner (7 examples). A borinic acid functionalized 1,4‐B,N‐anthracene 1 was found to display unprecedented reactivity, acting as a convenient and highly effective precursor for selective formation of bromo substituted B,N,B‐benzo[4]helicenes 2a / 2b via intramolecular borylation and sequential B‐Mes bond cleavage in presence of BBr 3 . Subsequent reaction of 2a / 2b with Ar‐Li provided a highly effective toolbox for the preparation of symmetrically/unsymmetrically functionalized B,N,B‐helicenes. Their high photoluminescence quantum yields along with the small Δ E ST suggest the potential as thermally activated delayed fluorescence (TADF) emitters for organic light‐emitting diodes (OLEDs). | en |
| dc.identifier.doi | https://doi.org/10.1002/anie.201912340 | |
| dc.identifier.uri | http://hdl.handle.net/1974/27527 | |
| dc.language.iso | en | en |
| dc.rights | This is the peer reviewed version of the following article: Intramolecular Borylation via Sequential B‐Mes Bond Cleavage for the Divergent Synthesis of B,N,B‐doped Benzo[4]helicenes, Angewandte chemie international edition, which has been published in final form at https://doi.org/10.1002/anie.201912340. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | en |
| dc.subject | Synthetic Methods | en |
| dc.subject | Boron | en |
| dc.subject | Luminescence | en |
| dc.subject | Heterocycles | en |
| dc.subject | Borylation | en |
| dc.title | Intramolecular Borylation via Sequential B‐Mes Bond Cleavage for the Divergent Synthesis of B,N,B‐doped Benzo[4]helicenes | en |
| dc.type | journal article | en |
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