scholarly journals A fluorescent pH probe for an aqueous solution composed of 7-hydroxycoumarin, Schiff base and phenanthro[9,10-d]imidazole moieties (PICO)

2018 ◽  
Vol 24 (2) ◽  
pp. 93-97
Author(s):  
Shaoxin Li ◽  
Wei Kan ◽  
Bing Zhao ◽  
Ting Liu ◽  
Yue Fang ◽  
...  

AbstractThe pH fluorescent probe 7-hydroxy-4-methyl-8-(((2-(1-phenyl-1H-phenanthro[9,10-d]imidazol-2-yl)phenyl)imino)methyl)-2H-chromen-2-one (PICO) contains a donor–π–acceptor (D–π–A) conjugated system. The ‘off−on’ probe PICO has a pKa value of 8.01 and its fluorescence intensity is enhanced with increasing pH.

2020 ◽  
Vol 44 (45) ◽  
pp. 19642-19649
Author(s):  
Lingjie Hou ◽  
Tao Liu ◽  
Yaling Gong ◽  
Jin Li ◽  
Chenhua Deng ◽  
...  

A Schiff base fluorescent probe, namely naphthalic anhydride – (2-pyridine) hydrazone (NAH), has been synthesized and developed for the highly selective and sensitive monitoring of Fe3+ ions in an aqueous solution and living cells.


2018 ◽  
Vol 34 (9) ◽  
pp. 1079-1083 ◽  
Author(s):  
Huixian JIA ◽  
Chenghong FENG ◽  
Chenhao TIAN

2017 ◽  
Vol 5 (2) ◽  
pp. 024014 ◽  
Author(s):  
Peng-Cheng Huang ◽  
Hao Fang ◽  
Jing-Jing Xiong ◽  
Fang-Ying Wu

2018 ◽  
Vol 15 (1) ◽  
pp. 47-55
Author(s):  
Xuebing Li ◽  
Haifen Yang ◽  
Ning Wang ◽  
Tijian Sun ◽  
Wei Bian ◽  
...  

Background: Morin has many pharmacological functions including antioxidant, anticancer, anti-inflammatory, and antibacterial effects. It is commonly used in the treatment of antiviral infection, gastropathy, coronary heart disease and hepatitis B in clinic. However, researches have shown that morin is likely to show prooxidative effects on the cells when the amount of treatment is at high dose, leading to the decrease of intracellular ATP levels and the increase of necrosis process. Therefore, it is necessary to determine the concentration of morin in biologic samples. Method: Novel water-soluble and green nitrogen and sulfur co-doped carbon dots (NSCDs) were prepared by a microwave heating process with citric acid and L-cysteine. The fluorescence spectra were collected at an excitation wavelength of 350 nm when solutions of NSCDs were mixed with various concentrations of morin. Results: The as-prepared NSCDs were characterized by transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The fluorescence intensity of NSCDs decreased significantly with the increase of morin concentration. The fluorescence intensity of NSCDs displayed a linear response to morin in the concentration 0.10-30 μM with a low detection limit of 56 nM. The proposed fluorescent probe was applied to analysis of morin in human body fluids with recoveries of 98.0-102%. Conclusion: NSCDs were prepared by a microwave heating process. The present analytical method is sensitive to morin. The quenching process between NSCDs and morin is attributed to the static quenching. In addition, the cellular toxicity on HeLa cells indicated that the as-prepared NSCDs fluorescent probe does not show obvious cytotoxicity in cell imaging. Our proposed method possibly opens up a rapid and nontoxic way for preparing heteroatom doped carbon dots with a broad application prospect.


Author(s):  
Hong-Bo Liu ◽  
Hai Xu ◽  
Xin Guo ◽  
Jian Xiao ◽  
Zheng-Hong Cai ◽  
...  

A near-infrared (NIR) fluorescent probe with a large Stokes shift (143 nm) for the rapid identification of Cys over Hcy and GSH in aqueous solution was developed.


2021 ◽  
Vol 233 ◽  
pp. 117911
Author(s):  
Minmin Wang ◽  
Linxia Lu ◽  
Wenwu Song ◽  
Xunyue Wang ◽  
Tongming Sun ◽  
...  

1965 ◽  
Vol 18 (5) ◽  
pp. 651 ◽  
Author(s):  
RW Green ◽  
PW Alexander

The Schiff base, N-n-butylsalicylideneimine, extracts more than 99.8% beryllium into toluene from dilute aqueous solution. The distribution of beryllium has been studied in the pH range 5-13 and is discussed in terms of the several complex equilibria in aqueous solution. The stability constants of the complexes formed between beryllium and the Schiff base are log β1 11.1 and log β2 20.4, and the distribution coefficient of the bis complex is 550. Over most of the pH range, hydrolysis of the Be2+ ion competes with complex formation and provides a means of measuring the hydrolysis constants. They are for the reactions: Be(H2O)42+ ↔ 2H+ + Be(H2O)2(OH)2, log*β2 - 13.65; Be(H2O)42+ ↔ 3H+ + Be(H2O)(OH)3-, log*β3 -24.11.


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