2026-04-17T10:26:23Zhttps://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

00925njm 22002777a 4500 dc 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 author 2022-09 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. 0143-7208 http://hdl.handle.net/10259/7496 10.1016/j.dyepig.2022.110557 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