TY - JOUR
T1 - Narrowband Blue Circularly Polarized Luminescence Emitter Based on BN-Doped Benzo[6]helicene with Stimuli-Responsive Properties
AU - Liu, Meiyan
AU - Li, Chenglong
AU - Liao, Guanming
AU - Zhao, Fenggui
AU - Yao, Chunxia
AU - Wang, Nan
AU - Yin, Xiaodong
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/9/16
Y1 - 2024/9/16
N2 - Boron-doped helicenes, known for their unique electronic and photophysical properties, are of great interest for numerous applications. This research introduces two new azabora[6]helicenes, H[6]BN1 and H[6]BN2, synthesized through an efficient method. These molecules have boron and nitrogen atoms in opposing positions, enhancing their distinctive attributes. Both helicenes show excellent emission properties, with H[6]BN1 and H[6]BN2 exhibiting narrowband blue fluorescence and circularly polarized luminescence (CPL), achieving glum values of 4~5×10−4 which is beneficial for chiroptical applications. The addition of a donor group, 3, 6-di-tert-butyl-9H-carbazole, in H[6]BN2 improves luminescence, likely due to enhanced molecular orbital overlap and electron delocalization. H[6]BN1′s needle-like single crystals exhibit mechanochromism, changing luminescent color from yellow to green under mechanical stress, which is promising for stimulus-responsive materials. In conclusion, this study presents a novel class of BN[6]helicenes with superior chiroptical properties. Their combination of electronic features and mechanochromism makes them ideal for advanced chiroptical materials, expanding the potential of helicene-based compounds and offering new directions for the synthesis of molecules with specific chiroptical characteristics.
AB - Boron-doped helicenes, known for their unique electronic and photophysical properties, are of great interest for numerous applications. This research introduces two new azabora[6]helicenes, H[6]BN1 and H[6]BN2, synthesized through an efficient method. These molecules have boron and nitrogen atoms in opposing positions, enhancing their distinctive attributes. Both helicenes show excellent emission properties, with H[6]BN1 and H[6]BN2 exhibiting narrowband blue fluorescence and circularly polarized luminescence (CPL), achieving glum values of 4~5×10−4 which is beneficial for chiroptical applications. The addition of a donor group, 3, 6-di-tert-butyl-9H-carbazole, in H[6]BN2 improves luminescence, likely due to enhanced molecular orbital overlap and electron delocalization. H[6]BN1′s needle-like single crystals exhibit mechanochromism, changing luminescent color from yellow to green under mechanical stress, which is promising for stimulus-responsive materials. In conclusion, this study presents a novel class of BN[6]helicenes with superior chiroptical properties. Their combination of electronic features and mechanochromism makes them ideal for advanced chiroptical materials, expanding the potential of helicene-based compounds and offering new directions for the synthesis of molecules with specific chiroptical characteristics.
KW - 1, 4-Azaborinine [6]helicenes
KW - Circularly polarized luminescence
KW - Mechanochromism
KW - Narrowband blue photoluminescence
KW - Organic light-emitting diodes
UR - http://www.scopus.com/inward/record.url?scp=85201422484&partnerID=8YFLogxK
U2 - 10.1002/chem.202402257
DO - 10.1002/chem.202402257
M3 - Article
AN - SCOPUS:85201422484
SN - 0947-6539
VL - 30
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 52
M1 - e202402257
ER -