scholarly journals Determination of Enantiomeric Excess by Solid-Phase Extraction Using a Chiral Metal-Organic Framework as Sorbent

Molecules ◽  
2018 ◽  
Vol 23 (11) ◽  
pp. 2802
Author(s):  
Jun-Hui Zhang ◽  
Bo Tang ◽  
Sheng-Ming Xie ◽  
Bang-Jin Wang ◽  
Mei Zhang ◽  
...  

Metal-organic frameworks (MOFs) have recently attracted considerable attention because of their fascinating structures and intriguing potential applications in diverse areas. In this study, we developed a novel method for determination of enantiomeric excess (ee) of (±)-1,1′-bi-2-naphthol by solid-phase extraction (SPE) using a chiral MOF, [Co(l-tyr)]n(l-tyrCo), as sorbent. After optimization of the experimental conditions, a good linear relationship between the ee and the absorbance of the eluate (R2 = 0.9984) was obtained and the standard curve was established at the concentration of 3 mmol L−1. The ee values of (±)-1,1′-bi-2-naphthol samples can be rapidly calculated using the standard curve after determination of the absorbance of the eluate. The method showed good accuracy, with an average error of 2.26%, and is promising for ee analysis.

2018 ◽  
Vol 42 (8) ◽  
pp. 5806-5813 ◽  
Author(s):  
Rohullah Kashanaki ◽  
Homeira Ebrahimzadeh ◽  
Morteza Moradi

D-μ-SPE-SUPRAS-ME followed by GFAAS was successfully used for preconcentration and determination of copper in real samples.


2019 ◽  
Vol 11 (27) ◽  
pp. 3467-3473 ◽  
Author(s):  
Zhiyang Lv ◽  
Cheng Yang ◽  
Yuehong Pang ◽  
Weiying Xie ◽  
Xiaofang Shen

Metal–organic frameworks MIL-101(Cr) has high efficiency for dispersive solid-phase extraction of benzo(a)pyrene in edible oil by π–π interaction and size effect.


BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Massoud Kaykhaii ◽  
Sayyed Hossein Hashemi ◽  
Fariba Andarz ◽  
Amin Piri ◽  
Ghasem Sargazi ◽  
...  

Abstract Background A chromium-based metal organic framework was synthesized and employed as an efficient sorbent for pipette tip micro-solid phase extraction and preconcentration of parabens from wastewater and shampoo samples up to sub-ppb level before their spectrophotometric analysis. Results Factors affecting preconcentration including volume and type of solvent, amount of sorbent, number of extraction, and volume and pH of samples were optimized employing one-variable-at-a-time and response surface methodology. Obtained analytical characteristics of the method proves its usefulness for analysis of real samples. Linear range of the method for parabens was 1.0–200.0 μg/L. Detection limit of the protocol was 0.24 µg/L for propyl paraben and 0.25 µg/L for methyl paraben. Reproducibility of the protocol defined as % RSD was better than 5.78%. Synthesized adsorbent can be re-used for at least 20 extractions. Conclusion The method showed a good detection limit and precision for determination of methyl- and propyl-paraben in wastewater and shampoo samples.


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