Effect of Tartaric Acid on the Electrochemical Behavior of K3[Fe(CN)6] on the Electrodes Coated with Cyclodextrin Modified Multi-Walled Carbon Nanotubes

2013 ◽  
Vol 781-784 ◽  
pp. 346-351
Author(s):  
Hai Tao Wang ◽  
Shi Zhao Kang ◽  
Qiu Ling Yang ◽  
Jin Mu

The effect of tartaric acid on the electrochemical behavior of K3[Fe(CN)6] was investigated on bare ITO electrodes, electrodes coated with multi-walled carbon nanotubes possessing carboxyl groups (MWNT-COOHs), and electrodes coated with cyclodextrin modified multi-walled carbon nanotubes (MWNT-CDs), respectively. It is found that the molecular chirality of tartaric acid can hardly influence the electrochemical behavior of K3[Fe(CN)6] on bare ITO electrodes. When the electrodes coated with MWNT-COOHs are used, the effect of the molecular chirality becomes distinguish. In the case of the electrodes coated with MWNT-CDs, the enhanced chiral discrimination between D-tartaric acid (D-TA) and L-tartaric acid (L-TA) can be observed. The control step in the electrochemical reaction of K3[Fe(CN)6] on the electrodes coated with MWNT-CDs is deduced to be different when D-TA or L-TA is introduced into the solution, respectively. Therefore, the enhanced chiral discrimination on the electrodes coated with MWNT-CDs is probably due to the change of the control step in the electrochemical reaction of K3[Fe(CN)6] caused by the chiral recognition of cyclodextrin moieties to D-TA and L-TA.

The Analyst ◽  
2014 ◽  
Vol 139 (9) ◽  
pp. 2243-2248 ◽  
Author(s):  
Lisha Chen ◽  
Fengxia Chang ◽  
Lingchen Meng ◽  
Meixian Li ◽  
Zhiwei Zhu

The combination of SWV with chiral SWCNTs and H2SO4 shows chiral discrimination for 3,4-dihydroxyphenylalanine, and the three are indispensable for this chiral recognition.


2012 ◽  
Vol 602-604 ◽  
pp. 278-280
Author(s):  
Zhi Guang Peng ◽  
Dong Hong Yin ◽  
Jian Fu Liu ◽  
Jin Gang Yu ◽  
Xiao Na Yang ◽  
...  

The oxidized multi-walled carbon nanotubes were prepared by a nitric acid treatment procedure, which were then used as additive in thin-layer chromatography stationary phases for resolution of ofloxacin, mandelic acid and 2-chloro-mandelic acid enantiomers. In a sharp contrast with pristine multi-walled carbon nanotubes/D-(-)-tartaric acid impregnated thin-layer chromatography plates, oxidized multi-walled carbon nanotubes/D-(-)-tartaric acid impregnated plates presented better enantioseparation effects for ofloxacin enantiomers.


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