Intermolecular proton-transfer in acetic acid clusters induced by vacuum-ultraviolet photoionization

2009 ◽  
Vol 131 (18) ◽  
pp. 184304 ◽  
Author(s):  
Keisuke Ohta ◽  
Yoshiyuki Matsuda ◽  
Naohiko Mikami ◽  
Asuka Fujii
2017 ◽  
Vol 147 (19) ◽  
pp. 194302 ◽  
Author(s):  
Marta Berholts ◽  
Hanna Myllynen ◽  
Kuno Kooser ◽  
Eero Itälä ◽  
Sari Granroth ◽  
...  

Molecules ◽  
2022 ◽  
Vol 27 (2) ◽  
pp. 516
Author(s):  
You Qian ◽  
Fuchun Gong ◽  
Jiguang Li ◽  
Pan Ma ◽  
Hanming Zhu ◽  
...  

Constructing excited-state intermolecular proton transfer (ESIPT-e) fluorophores represents significant challenges due to the harsh requirement of bearing a proton donor-acceptor (D-A) system and their matching proton donating-accepting ability in the same molecule. Herein, we synthesized a new-type ESIPT-e fluorophor (2-APC) using the “four-component one-pot” reaction. By the installing of a cyano-group on pyridine scaffold, the proton donating ability of -NH2 was greatly enhanced, enabling 2-APC to undergo ESIPT-e process. Surprisingly, 2-APC exhibited dual-emissions in protic solvents ethanol and normal fluorescence in aprotic solvents, which is vastly different from that of conventional ESIPT-a dyes. The ESIPT emission can be obviously suppressed by Fe3+ due to the coordination reaction of Fe3+ with the A-D system in 2-APC. From this basis, a highly sensitive and selective method was established using 2-APC as a fluorescent probe, which offers the sensitive detection of Fe3+ ranging from 0 to 13 μM with the detection limit of 7.5 nM. The recovery study of spiked Fe3+ measured by the probe showed satisfactory results (97.2103.4%) with the reasonable RSD ranging from 3.1 to 3.8%. Moreover, 2-APC can also exhibit aggregation-induced effect in poor solvent or solid-state, eliciting strong red fluorescence. 2-APC was also applied to cell-imaging, exhibiting good cell-permeability, biocompatibility and color rendering. This multi-mode emission of 2-APC is significant departure from that of conventional extended p-conjugated systems and ESIPT dyes based on a flat and rigid molecular design. The “one-pot synthesis” strategy for the construction of ESIPT molecules pioneered a new route to achieve tricolor-emissive fluorophores.


2003 ◽  
Vol 107 (18) ◽  
pp. 3244-3253 ◽  
Author(s):  
Fa-Tsai Hung ◽  
Wei-Ping Hu ◽  
Tsung-Hui Li ◽  
Chung-Chih Cheng ◽  
Pi-Tai Chou

2005 ◽  
Vol 127 (18) ◽  
pp. 6641-6651 ◽  
Author(s):  
Agam R. Sheth ◽  
Joseph W. Lubach ◽  
Eric J. Munson ◽  
Francis X. Muller ◽  
David J. W. Grant

2005 ◽  
Vol 122 (20) ◽  
pp. 204304 ◽  
Author(s):  
Rafał A. Bachorz ◽  
Maciej Harańczyk ◽  
Iwona Dąbkowska ◽  
Janusz Rak ◽  
Maciej Gutowski

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