TY - JOUR
T1 - Voltammetric method for determining the trace moisture content of organic solvents based on hydrogen-bonding interactions with quinones
AU - Hui, Yanian
AU - Chng, Elaine Lay Khim
AU - Chua, Louisa Pei Lyn
AU - Liu, Wan Zhen
AU - Webster, Richard D.
PY - 2010/3/1
Y1 - 2010/3/1
N2 - Voltammetry experiments were performed on the natural quinone, vitamin K1 (VK1), in a range of organic solvents of varying dielectric constant that are commonly used for electrochemicalmeasurements [dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), acetonitrile (MeCN), propionitrile (EtCN), butyronitrile (PrCN), 1,2-dichloroethane (DCE), dichloromethane (DCM), and 1,1,2,2tetrachloroethane (TCE)]. The water content of the solvents was accurately measured using Karl Fischer (KF) coulometric titrations, and the voltammetric data were used to estimate the degree of hydrogen-bonding interactions between the reduced forms of VK1 and variable levels of water, thereby allowing a ranking of watersubstrate interactions in the different solvents. The voltammetric data were analyzed based on interactions that occur between reduced forms of VK1 and the water, the solvent, and the supporting electrolyte. Calibration data were obtained that are independent of me nature of the reference electrode and allow the water content of the solvents to be calculated by performing a single voltammetric scan in the presence of VK1 and 0.2 M supporting electrolyte (Bu4NPF6).
AB - Voltammetry experiments were performed on the natural quinone, vitamin K1 (VK1), in a range of organic solvents of varying dielectric constant that are commonly used for electrochemicalmeasurements [dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), acetonitrile (MeCN), propionitrile (EtCN), butyronitrile (PrCN), 1,2-dichloroethane (DCE), dichloromethane (DCM), and 1,1,2,2tetrachloroethane (TCE)]. The water content of the solvents was accurately measured using Karl Fischer (KF) coulometric titrations, and the voltammetric data were used to estimate the degree of hydrogen-bonding interactions between the reduced forms of VK1 and variable levels of water, thereby allowing a ranking of watersubstrate interactions in the different solvents. The voltammetric data were analyzed based on interactions that occur between reduced forms of VK1 and the water, the solvent, and the supporting electrolyte. Calibration data were obtained that are independent of me nature of the reference electrode and allow the water content of the solvents to be calculated by performing a single voltammetric scan in the presence of VK1 and 0.2 M supporting electrolyte (Bu4NPF6).
UR - http://www.scopus.com/inward/record.url?scp=77749305091&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77749305091&partnerID=8YFLogxK
U2 - 10.1021/ac9026719
DO - 10.1021/ac9026719
M3 - Article
AN - SCOPUS:77749305091
SN - 0003-2700
VL - 82
SP - 1928
EP - 1934
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 5
ER -