2023
DOI: 10.1039/d2tc04447a
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Facile dimerization strategy for producing narrowband green multi-resonance delayed fluorescence emitters

Abstract: Establishing a simple molecular design strategy for enabling redshifted emissions while maintaining high color purity in multi-resonance thermally activated delayed fluorescence (MR-TADF) remains a crucial yet challenging task. Herein, we...

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Cited by 17 publications
(12 citation statements)
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“…116,130,131,133,168,169 DOBNA and CzBN derivatives bearing boronic ester groups, which engage in Suzuki–Miyaura coupling with aryl halides, can be synthesised from brominated derivatives via Miyaura–Ishiyama borylation or iridium-catalysed direct aromatic C–H (Hartwig–Miyaura) borylation (Scheme 40). 118,135,185,259–261 An asymmetric bridge with N and O atoms was also demonstrated. 95…”
Section: Late-stage Functionalisationmentioning
confidence: 90%
See 1 more Smart Citation
“…116,130,131,133,168,169 DOBNA and CzBN derivatives bearing boronic ester groups, which engage in Suzuki–Miyaura coupling with aryl halides, can be synthesised from brominated derivatives via Miyaura–Ishiyama borylation or iridium-catalysed direct aromatic C–H (Hartwig–Miyaura) borylation (Scheme 40). 118,135,185,259–261 An asymmetric bridge with N and O atoms was also demonstrated. 95…”
Section: Late-stage Functionalisationmentioning
confidence: 90%
“…13, 14 and Tables 13, 14). 172–187 Although a methoxy group was deprotected by BBr 3 in the one-pot borylation procedure (Scheme 4), the methylthio (SMe) group was preserved under the same conditions ( BN(p)SCH 3 , Fig. 13).…”
Section: One-pot Borylationmentioning
confidence: 99%
“…6n), by a facile dimerization strategy. 71 In a deoxygenated toluene solution, both p -CzB and m -CzB exhibited pure green emissions at 505 and 515 nm with narrow spectral FWHMs of 34 and 35 nm, respectively. The Δ E ST values of p -CzB and m -CzB were determined to be 0.17 and 0.13 eV, respectively.…”
Section: Design Strategies For Mr-tadf Emittersmentioning
confidence: 93%
“…Among the reported boron based acceptors, the fully fused oxygen bridged triarylboron, 5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene (DOBNA) attracted significant attention because of its unique properties such as multi-resonance feature, rigid molecular structure, narrowband emission, and excellent TADF characteristics (Figure 3). [52][53][54][55][56][86][87][88][89] Consequently, numerous DOB-NA-based TADF emitters have been developed by adopting different molecular designs and achieved very high EQE. However, these materials often displayed severe efficiency rolloff and poor operational stability, which needs to be addressed from the molecular design perspective.…”
Section: Introductionmentioning
confidence: 99%