2026-06-29T20:23:54Zhttps://riubu.ubu.es/oai/request

oai: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

Busto Vázquez, Natalia Romero Velásquez, Daisy Carolina Revilla Cuesta, Andrea Abajo Cuadrado, Irene Cuevas Vicario, José Vicente Rodríguez Rodríguez, Mª Teresa García Ruiz, Begoña 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 http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess 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