2018
DOI: 10.1021/acs.jpclett.8b01511
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Design of Conformationally Distorted Donor–Acceptor Dyads Showing Efficient Thermally Activated Delayed Fluorescence

Abstract: A highly potent donor-acceptor biaryl thermally activated delayed fluorescence (TADF) dye is accessible by a concise two-step sequence employing two-fold Ullmann arylation and a sequentially Pd-catalyzed Masuda borylation-Suzuki arylation (MBSA). Photophysical investigations show efficient TADF at ambient temperature due to the sterical hindrance between the donor and acceptor moieties. The photoluminescence quantum yield amounts to Φ = 80% in toluene and 90% in PMMA arising from prompt and delayed fluorescenc… Show more

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Cited by 40 publications
(48 citation statements)
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“…1e). 8 a This is in contrast with previously reported through-space charge transfer TADF emitters in which through-space D–A interaction minimizes the electron-exchange energy and induces a narrow Δ E ST 19. However, the larger overlap integral of frontier orbitals increases the transition dipole moment and thus results in a faster prompt decay.…”
Section: Resultsmentioning
confidence: 80%
“…1e). 8 a This is in contrast with previously reported through-space charge transfer TADF emitters in which through-space D–A interaction minimizes the electron-exchange energy and induces a narrow Δ E ST 19. However, the larger overlap integral of frontier orbitals increases the transition dipole moment and thus results in a faster prompt decay.…”
Section: Resultsmentioning
confidence: 80%
“…While for singlet harvesting, the molecules have to show efficient thermally activated delayed fluorescence (TADF) at ambient temperature. Examples are found among Cu(I), Ag(I), Au(III), W(VI) and Zn(II) complexes [ 7 , 9 , 10 , 11 , 12 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 , 60 , 61 , 62 , 63 , 64 , 65 ] or specifically designed organic molecules [ 66 , 67 , 68 , 69 , 70 , 71 , 72 , 73 , 74 , 75 , 76 ,…”
Section: Introductionmentioning
confidence: 99%
“…In addition, TADF materials with different donor moieties such as 9,9-dimethyl-9,10-dihydroacridine, 10H-phenoxazine, 5,10-dihydrophenazine, 10H-phenothiazine, 9H-carbazole, 3,6-di-tert-butyl-9H-carbazole, 9,9-diphenyl-9,10dihydroacridine 9H-spiro[4,5]fluorene-9,10-dihydroacridine, 9-(3-(9H-carbazol-9-yl)phenyl)-9H-carbazole, and diphenylamine possess excellent electroluminescence performance (Bezvikonnyi et al, 2019;Hosokai et al, 2019;Jin et al, 2019;Joo et al, 2019;Kim et al, 2019;Sharma et al, 2019;Zhong et al, 2019). Meanwhile, there are many TADF materials with different acceptor moieties such as benzonitrile, triazines, sulfones, benzophenone, quinoxaline, and naphthalimide reported in literature (Li et al, 2016;Nobuyasu et al, 2016;Tsujimoto et al, 2017;Sommer et al, 2018;Wu et al, 2018;Yu et al, 2018). The HOMO/LUMO distribution and energy levels of the typical donor and acceptor moieties have been found in the relevant literature (Im et al, 2017b).…”
Section: Introductionmentioning
confidence: 99%