@article{Dash:2019:10.1039/c8tc05131c,
author = {Dash, BP and Hamilton, I and Tate, DJ and Crossley, D and Kim, J-S and Ingleson, MJ and Turner, M},
doi = {10.1039/c8tc05131c},
journal = {Journal of Materials Chemistry C},
pages = {718--724},
title = {Benzoselenadiazole and benzotriazole directed electrophilic C-H borylation of conjugated donor-acceptor materials},
url = {http://dx.doi.org/10.1039/c8tc05131c},
volume = {7},
year = {2019}
}

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TY  - JOUR
AB  - Benzoselenadiazole and benzotriazole directed electrophilic borylation using BCl3 results in the C–H functionalization of an adjacent aromatic unit and produces fused boracycles. Subsequent arylation at boron afforded air and moisture stable products displaying large bathochromic shifts and significantly reduced LUMO energy levels. OLEDs fabricated containing borylated benzoselenadiazole derivatives showed emission centered at 723 nm in the near infra-red region of the spectrum.
AU  - Dash,BP
AU  - Hamilton,I
AU  - Tate,DJ
AU  - Crossley,D
AU  - Kim,J-S
AU  - Ingleson,MJ
AU  - Turner,M
DO  - 10.1039/c8tc05131c
EP  - 724
PY  - 2019///
SN  - 2050-7526
SP  - 718
TI  - Benzoselenadiazole and benzotriazole directed electrophilic C-H borylation of conjugated donor-acceptor materials
T2  - Journal of Materials Chemistry C
UR  - http://dx.doi.org/10.1039/c8tc05131c
UR  - http://hdl.handle.net/10044/1/66159
VL  - 7
ER  - 

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