Journal Article PUBDB-2024-04817

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Borylation and rearrangement reactions of azasilaanthracenes to afford B,N-doped nanographenes

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2024
Royal Society of Chemistry London

Dalton transactions 53(22), 9294-9300 () [10.1039/D4DT01166J]
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Abstract: An air-stable B3,N3-containing dibenzobisanthene (8) was prepared in 29% yield by heating a 1,3,5-tri(aza silaanthryl)benzene (5) with BBr3 (180 °C). Under these conditions, the reaction does not stop after three fold SiMe2/BBr exchange but proceeds further via two rearrangement and two intramolecular C–H borylation steps. Some mechanistic details were unveiled by using smaller model systems and applying lower reaction temperatures. According to X-ray crystallography, compound 8 has a helically distorted scaffold. Due to its multiple resonance structure, it shows a narrow-band blue-green emission (λem = 493 nm; ΦPL = 84%; FWHM = 0.20 eV; THF); samples measured in PMMA gave prompt and delayed fluorescence lifetimes of 10.7 ns and 136 µs, respectively. The optical properties of 8 and of structurally related species were also investigated by quantum-chemical means: most of these compounds exhibit a small energy gap ΔEST between the lowest excited singlet (S1) and triplet (T1) states and a non-negligible spin–orbit coupling (SOC) between S1 and T1/T2, demonstrating their potential as thermally activated delayed fluor escence (TADF) emitters

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Contributing Institute(s):
  1. DOOR-User (DOOR ; HAS-User)
Research Program(s):
  1. 6G3 - PETRA III (DESY) (POF4-6G3) (POF4-6G3)
  2. FS-Proposal: I-20220822 (I-20220822) (I-20220822)
Experiment(s):
  1. PETRA Beamline P24 (PETRA III)

Appears in the scientific report 2024
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Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; Chemical Reactions ; Clarivate Analytics Master Journal List ; Current Contents - Physical, Chemical and Earth Sciences ; Ebsco Academic Search ; Essential Science Indicators ; IF < 5 ; JCR ; National-Konsortium ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2024-06-20, last modified 2025-07-23


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