2026-04-17T11:43:25Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/74962023-04-17T13:15:00Zcom_10259_4363com_10259_5086com_10259_2604com_10259_3592com_10259_3591com_10259.4_106com_10259_4354com_10259_4365col_10259_4364col_10259_3930col_10259_4355col_10259_4366
Repositorio Institucional de la Universidad de Burgos
author
Busto Vázquez, Natalia
author
Romero Velásquez, Daisy Carolina
author
Revilla Cuesta, Andrea
author
Abajo Cuadrado, Irene
author
Cuevas Vicario, José Vicente
author
Rodríguez Rodríguez, Mª Teresa
author
García Ruiz, Begoña
author
Torroba Pérez, Tomás
2023-03-06T12:39:20Z
2023-03-06T12:39:20Z
2022-09
0143-7208
http://hdl.handle.net/10259/7496
10.1016/j.dyepig.2022.110557
A new series of perylene and hemicoronene diimides, obtained by visible light photocyclization, are presented,
between them some remarkable examples that are soluble in only water, and give nanoparticles by selfassociation. Those compounds work as new fluorescent materials in water by complexation with cucurbit[7]
uril, as well as selective G-quadruplex binding ligands with remarkable cytotoxic activity when the interaction
with G4 was sufficiently strong.
eng
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Perylenediimides
Hemicoronenediimides
Photocyclization
Nanoparticles
G-quadruplex
Cucurbituril
Cytotoxicity
Synthesis of water-soluble hemicoronenediimides by photocyclization of perylenediimides: Turn-on fluorescent probes in water by complexation with Cucurbit[7]uril or binding to G-quadruplex Motifs
info:eu-repo/semantics/article
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URL
https://riubu.ubu.es/bitstream/10259/7496/1/Busto-dp_2022.pdf
File
MD5
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6342681
application/pdf
Busto-dp_2022.pdf