Hyperfluorescent polymers enabled by through-space charge transfer polystyrene sensitizers for high-efficiency and full-color electroluminescence

J Hu, Y Wang, Q Li, S Shao, L Wang, X Jing… - Chemical Science, 2021 - pubs.rsc.org
Fluorescent polymers are suffering from low electroluminescence efficiency because triplet
excitons formed by electrical excitation are wasted through nonradiative pathways. Here we …

Highly efficient and non-doped red conjugated polymer dot for photostable cell imaging

M Wu, Q Wei, C Xian, C Dai, X He, C Wu, G Sun… - Chinese Chemical …, 2023 - Elsevier
By introducing a naphthothiadiazole (NT) unit as the main building block, a non-doped and
red emissive conjugated polymer poly (9, 9-dihexylfluorene-alt-naphthothiadiazole)(PFNT) …

Fluorescent benzoselenadiazoles: synthesis, characterization, and quantification of intracellular lipid droplets and multicellular model staining

IR Medeiros, JR Corrêa, ALA Barbosa… - The Journal of …, 2020 - ACS Publications
In this work, we described the synthesis of 10 new fluorescent 2, 1, 3-benzoselenadiazole
small-molecule derivatives and their chemical-and photocharacterizations. The new …

New red-emitting conjugated polyelectrolyte: Stabilization by interaction with biomolecules and potential use as drug carriers and bioimaging probes

Z Kahveci, R Vazquez-Guillo… - … applied materials & …, 2016 - ACS Publications
The design and development of fluorescent conjugated polyelectrolytes (CPEs) emitting in
the red region of the visible spectrum is at present of great interest for bioimaging studies …

Electrochemical and Solvent‐Mediated Visible‐to‐Near‐Infrared Spectroscopic Switching of Benzoselenadiazole Fluorophores

M Wałęsa‐Chorab, C Yao, G Tuner… - … –A European Journal, 2020 - Wiley Online Library
A series of electronic push–pull, pull–pull, and push fluorophores has been prepared from a
benzoselenadiazole core so that their spectroscopic, electrochemical, spectro …

Fused bis-benzothiadiazoles as electron acceptors

D Xia, XY Wang, X Guo, M Baumgarten… - Crystal Growth & …, 2016 - ACS Publications
Fused bis-benzothiadiazoles with different molecular geometries, namely, linear
benzoquinone-fused bis (benzothiadiazole)(Q-BBT) and V-shaped sulfone-fused bis …

Bisarylselanylbenzo‐2, 1, 3‐selenadiazoles: Synthesis, Photophysical, Electrochemical and Singlet‐Oxygen‐Generation Properties

RA Balaguez, R Krüger, B Iepsen… - European Journal of …, 2018 - Wiley Online Library
We describe herein our results on the synthesis of bisarylselanylbenzo‐2, 1, 3‐
selenadiazoles through double cross‐coupling reaction. The named compounds were …

Symmetrical and Unsymmetrical 4, 7‐Bis‐arylvinyl‐benzo‐2, 1, 3‐chalcogenodiazoles: Synthesis, Photophysical and Electrochemical Properties and Biomolecular …

R Krüger, B Iepsen, AME Larroza… - European Journal of …, 2020 - Wiley Online Library
Double Heck cross‐coupling reactions for the synthesis of 4, 7‐bis‐arylvinyl‐benzo‐2, 1, 3‐
chalcogenodiazole derivatives starting from 4, 7‐dibromobenzo [c][1, 2, 5] …

Synthesis and characterization of novel red-emitting conjugated polymers based on triphenylaminesilole-carbazole-fluorene

Z Liu, L Zhang, X Gao, Q Zhang, S Shi - Materials Chemistry and Physics, 2018 - Elsevier
A series of novel red-emitting conjugated polymers were synthesized, adopting host-guest
technique, with fluorene-carbazole backbone and low bandgap unit, 1, 1-dimethyl-3, 4-di …

Synthesis, optical and electrochemical properties of novel D-π-A type conjugated polymers based on benzo [c][1, 2, 5] selenadiazole unit via alkyne module

D Li, H Li, M Liu, J Chen, J Ding, X Huang, H Wu - Polymer, 2013 - Elsevier
Three novel donor-π-acceptor (D-π-A) type conjugated polymers P-1, P-2, and P-3 based on
benzo [c][1, 2, 5] selenadiazole moiety and phenyl or naphthyl group via alkyne module …