TY - JOUR
T1 - Anodic oxidation of ArSi(OEt)3 derivatives
AU - Dhiman, Anand
AU - Shi, Deqing
AU - Minge, Oliver
AU - Schmidbaur, Hubert
AU - Becker, James Y.
PY - 2006/6/15
Y1 - 2006/6/15
N2 - The electrochemical properties of 13 derivatives of triethoxysilylarenes [ArSi(OEt)3] have been studied in acetonitrile by cyclic voltammetry (CV). They all afford irreversible oxidation waves, mostly two, but some exhibit up to four waves. No reduction waves were detected on glassy upon scanning negatively up to -2.5 V. As expected, their oxidation has been found to be easier than their aryl silanes analogs (ArSiH3), presumably due to the participation of the lone-pair of the oxygen atoms of the ethoxy groups in the initial anodic process. By examining the surface effect, no significant difference in peak potentials was observed at Pt or GC working electrodes. Anodic oxidation of various substrates by controlled-potential electrolysis (CPE) in acetonitrile led mostly to polymers, except for the fully substituted derivative, Me5C6Si(OEt)3. It was oxidized both in acetonitrile and methanol, and yielded monomeric and dimeric products, respectively, all stemmed from C-Si bonds cleavage. The nature of products and mechanism of their formation are discussed.
AB - The electrochemical properties of 13 derivatives of triethoxysilylarenes [ArSi(OEt)3] have been studied in acetonitrile by cyclic voltammetry (CV). They all afford irreversible oxidation waves, mostly two, but some exhibit up to four waves. No reduction waves were detected on glassy upon scanning negatively up to -2.5 V. As expected, their oxidation has been found to be easier than their aryl silanes analogs (ArSiH3), presumably due to the participation of the lone-pair of the oxygen atoms of the ethoxy groups in the initial anodic process. By examining the surface effect, no significant difference in peak potentials was observed at Pt or GC working electrodes. Anodic oxidation of various substrates by controlled-potential electrolysis (CPE) in acetonitrile led mostly to polymers, except for the fully substituted derivative, Me5C6Si(OEt)3. It was oxidized both in acetonitrile and methanol, and yielded monomeric and dimeric products, respectively, all stemmed from C-Si bonds cleavage. The nature of products and mechanism of their formation are discussed.
KW - Carbon-silicon bond cleavage
KW - Cyclic voltammetry of triethoxysilylarenes
KW - Electrochemical oxidation
UR - https://www.scopus.com/pages/publications/33744988956
U2 - 10.1016/j.jelechem.2006.03.044
DO - 10.1016/j.jelechem.2006.03.044
M3 - Article
AN - SCOPUS:33744988956
SN - 1572-6657
VL - 591
SP - 127
EP - 132
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
IS - 2
ER -