Flexible Luminescent MOF: Trapping of Less Stable Conformation of Rotational Isomers, In Situ Guest-Responsive Turn-Off and Turn-On Luminescence and Mechanistic Study

2020 ◽  
Vol 12 (19) ◽  
pp. 22335-22346 ◽  
Author(s):  
Sajal Khatua ◽  
Protap Biswas
2021 ◽  
Vol 1157 ◽  
pp. 338394
Author(s):  
Xiao-Yue Tang ◽  
Yi-Ming Liu ◽  
Xiao-Lin Bai ◽  
Hao Yuan ◽  
Yi-Kao Hu ◽  
...  

2017 ◽  
Vol 23 (20) ◽  
pp. 4803-4809 ◽  
Author(s):  
Kwang Soo Lim ◽  
So Yeon Jeong ◽  
Dong Won Kang ◽  
Jeong Hwa Song ◽  
Hyuna Jo ◽  
...  

2017 ◽  
Vol 7 (20) ◽  
pp. 4669-4679 ◽  
Author(s):  
Zhouyang Liu ◽  
Vishnu Sriram ◽  
Can Li ◽  
Joo-Youp Lee

A mechanistic study using in situ DRIFTS and a kinetic study were conducted on a ruthenium oxide based mercury oxidation catalyst.


ChemPhotoChem ◽  
2022 ◽  
Author(s):  
Sébastien Jenni ◽  
Kévin Renault ◽  
Garance Dejouy ◽  
Sylvain Debieu ◽  
Myriam Laly ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-7 ◽  
Author(s):  
Xiaoxia Liu ◽  
Miaomiao Tian ◽  
Wenmei Gao ◽  
Jinzhong Zhao

An efficient, sensitive, and low-cost method has been developed for turn-on fluorescence sensing of dopamine (DA). The method relies on the rapid reaction of DA and 3-Hydroxyphenylboronic acid (3-HPBA) via specific recognition between boronic acids and cis-diol of DA in alkaline solution. The reaction product shows an excitation wavelength of 417 nm and the maximum emission peak at 470 nm. The proposed method allows the determination of DA in the range of 50 nM–25 μM, and the whole detection can be completed within 5 minutes. Furthermore, the presented approach has good selectivity and has been successfully applied to DA sensing in human serum samples, showing great potential in clinical diagnosis.


Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5236
Author(s):  
Maxime Balestrat ◽  
Abhijeet Lale ◽  
André Vinícius Andrade Bezerra ◽  
Vanessa Proust ◽  
Eranezhuth Wasan Awin ◽  
...  

The pyrolysis (1000 °C) of a liquid poly(vinylmethyl-co-methyl)silazane modified by tetrakis(dimethylamido)titanium in flowing ammonia, nitrogen and argon followed by the annealing (1000–1800 °C) of as-pyrolyzed ceramic powders have been investigated in detail. We first provide a comprehensive mechanistic study of the polymer-to-ceramic conversion based on TG experiments coupled with in-situ mass spectrometry and ex-situ solid-state NMR and FTIR spectroscopies of both the chemically modified polymer and the pyrolysis intermediates. The pyrolysis leads to X-ray amorphous materials with chemical bonding and ceramic yields controlled by the nature of the atmosphere. Then, the structural evolution of the amorphous network of ammonia-, nitrogen- and argon-treated ceramics has been studied above 1000 °C under nitrogen and argon by X-ray diffraction and electron microscopy. HRTEM images coupled with XRD confirm the formation of nanocomposites after annealing at 1400 °C. Their unique nanostructural feature appears to be the result of both the molecular origin of the materials and the nature of the atmosphere used during pyrolysis. Samples are composed of an amorphous Si-based ceramic matrix in which TiNxCy nanocrystals (x + y = 1) are homogeneously formed “in situ” in the matrix during the process and evolve toward fully crystallized compounds as TiN/Si3N4, TiNxCy (x + y = 1)/SiC and TiC/SiC nanocomposites after annealing to 1800 °C as a function of the atmosphere.


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