Abstract:Asymmetric blue multiple resonance type themally activated delayed fluorescence (TADF) materials composed of diphenylamine combined with carbazole and acridine units were synthesized and evaluated to finetune electronic and photophysical properties....
“…16 and Table 20). [202][203][204] In this procedure, the key intermediate possessing a boronic acid pinacol ester (Bpin) group is synthesised in high or moderate yield by the sequential addition of n BuLi and 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 6) with a comparable total yield (B40%). 120,124 Scheme 14 Example of sequential MR-TADF precursor construction reported in ref.…”
Section: 43mentioning
confidence: 99%
“…16 and Table 20). 202–204 In this procedure, the key intermediate possessing a boronic acid pinacol ester (Bpin) group is synthesised in high or moderate yield by the sequential addition of n BuLi and 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane ( i PrOBpin) to a bromine-containing precursor, with the subsequent intramolecular bora-Friedel–Crafts reaction affording fully cyclised target compounds.…”
This review highlights organoboron-based multiple-resonance compounds’ synthetic strategies classified as one-pot borylation, one-shot borylation, and late-stage functionalisation, and explores material structure–photophysical property correlations.
“…16 and Table 20). [202][203][204] In this procedure, the key intermediate possessing a boronic acid pinacol ester (Bpin) group is synthesised in high or moderate yield by the sequential addition of n BuLi and 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 6) with a comparable total yield (B40%). 120,124 Scheme 14 Example of sequential MR-TADF precursor construction reported in ref.…”
Section: 43mentioning
confidence: 99%
“…16 and Table 20). 202–204 In this procedure, the key intermediate possessing a boronic acid pinacol ester (Bpin) group is synthesised in high or moderate yield by the sequential addition of n BuLi and 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane ( i PrOBpin) to a bromine-containing precursor, with the subsequent intramolecular bora-Friedel–Crafts reaction affording fully cyclised target compounds.…”
This review highlights organoboron-based multiple-resonance compounds’ synthetic strategies classified as one-pot borylation, one-shot borylation, and late-stage functionalisation, and explores material structure–photophysical property correlations.
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