30612-17-0Relevant articles and documents
In situ generation of photoactivatable aggregation-induced emission probes for organelle-specific imaging
Li, Shiwu,Ling, Xia,Lin, Yuhan,Qin, Anjun,Gao, Meng,Tang, Ben Zhong
, p. 5730 - 5735 (2018)
Photoactivatable fluorescent probes are ideal tools for organelle study with a significant advantage of high spatiotemporal resolution. However, conventional photo-caged fluorophores for organelle-specific imaging suffer from several drawbacks, such as aggregation-caused quenching (ACQ), instability under ambient light, low photoactivation efficiency, and toxic photo-cleavage byproducts. Herein, we propose a strategy for in situ generation of photoactivatable aggregation-induced emission (AIE) probes of 2-(2-hydroxyphenyl)-benzothiazolines from easily available disulfide and thiol substrates through tandem S-S bond reduction and intramolecular cyclization reaction. Because the photoactivatable AIE probes can be in situ generated in a quantitative yield, they can be directly used for bio-imaging without complicated separation steps. Under both one- and NIR two-photon irradiation, excellent spatiotemporal resolution and high photoactivation efficiency were achieved for specific imaging of lipid droplets and lysosomes, respectively. Based on their in situ generation and adjustable organelle-targeting ability, the photoactivatable AIE probes could become an easy-to-use imaging tool in the study of the biological functions of organelles.
Imine-Amine Tautomerism vs Keto-Enol Tautomerism: Acceptor Basicity Dominates over Acceptor Electronegativity in the ESIPT Process through a Six-Membered Intramolecular H-Bonded Network
Bhattacharyya, Arghyadeep,Mandal, Sujoy Kumar,Guchhait, Nikhil
, p. 10246 - 10253 (2019)
Photophysical properties of a synthesized asymmetric two-way proton transfer molecule 3-(benzo[d]thiazol-2-yl)-2-hydroxy-5-methoxybenzaldehyde (BTHMB) were studied in detail. BTHMB could undergo excited-state intramolecular proton transfer (ESIPT) involvi
New Boron(III) Blue Emitters for All-Solution Processed OLEDs: Molecular Design Assisted by Theoretical Modeling
Salla, Cristian A. M.,Teixeira dos Santos, Jéssica,Farias, Giliandro,Bortoluzi, Adailton J.,Curcio, Sergio F.,Cazati, Thiago,Izsák, Róbert,Neese, Frank,de Souza, Bernardo,Bechtold, Ivan H.
supporting information, p. 2247 - 2257 (2019/04/08)
Luminescent boron(III) complexes have recently been employed as emitters in organic light-emitting diodes (OLEDs) with reasonable success. They are easy to prepare and sufficiently stable to be used in such devices, being of great interest as a simple mol