2022
DOI: 10.1039/d2sc01722a
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Access to tetracoordinate boron-doped polycyclic aromatic hydrocarbons with delayed fluorescence and aggregation-induced emission under mild conditions

Abstract: A series of tetracoordinate boron-doped polycyclic aromatic hydrocarbons have been synthesized under mild conditions, featuring delayed fluorescence and aggregation-induced emission.

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Cited by 24 publications
(11 citation statements)
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“…There are two types mainly utilized for the synthesis of the DB-MR-TADF emitters. These are (i) BuLi-based tandem borylation using Hunig base; (ii) One shot double borylation by using BBr 3 / BI 3 and reducing aromatic solvents 49,[83][84][85][86][87][88][89][90] . In type-1, under the inert atmosphere in the reducing solvents, the halogen will be replaced by using lithiation, and then transmetalation was done by using BBr 3 with the temperature controls [90][91][92][93] .…”
Section: Overall Synthetic Aspects For Borylationmentioning
confidence: 99%
“…There are two types mainly utilized for the synthesis of the DB-MR-TADF emitters. These are (i) BuLi-based tandem borylation using Hunig base; (ii) One shot double borylation by using BBr 3 / BI 3 and reducing aromatic solvents 49,[83][84][85][86][87][88][89][90] . In type-1, under the inert atmosphere in the reducing solvents, the halogen will be replaced by using lithiation, and then transmetalation was done by using BBr 3 with the temperature controls [90][91][92][93] .…”
Section: Overall Synthetic Aspects For Borylationmentioning
confidence: 99%
“…Doping four-coordinated boron atoms into π-conjugated systems could markedly decrease the LUMO level and increase the electron affinity, which is also true for π-conjugated systems consisting of 6-membered BN-chelate units. 192,208,209 In the subsection, we will focus on molecules with exceptionally low LUMO levels in different applications.…”
Section: Multi-bn-doped π-Conjugated Systems Bearing Tetracoordinate ...mentioning
confidence: 99%
“…26 This work not only provides a new family of MR BN-PAHs with facile synthesis procedures free of lithium reagents and with high yields, but also provides an opportunity to finely manipulate the electronic structures of BN-PAHs through B–N covalent bonds, which may uncover unforeseen optoelectronic properties. 27–30 However, at this initial stage, the performance of B–N embedded emitters still lags far behind their classical B,N-PAH counterparts. For instance, the FWHMs of those emitters are still larger than the cutting-edge values of B,N-MR emitters and they still need to demonstrate their color tunability for full-color emission.…”
Section: Introductionmentioning
confidence: 99%