, J. Am. Chem. Soc, vol.105, pp.4481-4483, 1983.
, Langmuir, vol.23, pp.1600-1607, 2007.
, J. Mater. Chem, vol.21, pp.2428-2444, 2011.
, Adv. Mater, vol.12, pp.1315-1328, 2000.
, Adv. Mater, pp.1447-1452, 2011.
, Chem. Phys. Lett, vol.29, pp.277-283, 1974.
, J. Mass Spectrom, vol.43, pp.1618-1626, 2008.
, Chem. Rev, vol.105, pp.1103-1169, 2005.
, Chem.-Eur. J, vol.15, pp.8128-8133, 2009.
, Science, vol.251, pp.919-922, 1991.
, Phys. Chem. Chem. Phys, vol.12, pp.12584-12590, 2010.
, J. Phys. Chem. C, vol.113, pp.1972-1979, 2009.
, Langmuir, vol.6, pp.682-691, 1990.
, J. Phys. Chem, vol.98, pp.563-571, 1994.
, Electrochem. Commun, vol.12, pp.1462-1466, 2010.
, J. Phys. Chem. B, vol.110, pp.24621-24628, 2006.
, Chemphyschem, vol.12, pp.769-771, 2011.
, Langmuir, vol.16, pp.9287-9293, 2000.
, Langmuir, vol.16, pp.5523-5525, 2000.
, Cl 2 , v ¼ 50 mV s À1 , in the presence of 40 mmol L À1 of sec-phenethyl alcohol. These SAMs were elaborated with (top) protocol A and (bottom) protocol B and prepared from C15T and (:) 1-dodecanethiol (C 12 SH), (-) 1-decanethiol (C 10 SH), (C) 1-octanethiol (C 8 SH), and (;) 1-hexanethiol (C 6 SH). Insets: segregation factor (f) deduced (eqn (2)) from experimental FWHMs of mixed SAMs used before catalytic experiments, CVs of mixed SAMs obtained in 0.1 M nBu4NPF 6 /CH 2
, J. Electroanal. Chem, vol.496, pp.29-36, 2001.
, Chemphyschem, vol.10, pp.2401-2404, 2009.
, Prog. Surf. Sci, vol.65, pp.151-256, 2000.
, J. Mass Spectrom, vol.41, pp.830-833, 2006.
, Electrochem. Commun, vol.16, pp.6-9, 2012.
, J. Am. Chem. Soc, vol.111, pp.321-335, 1989.
, Electrochemical Methods: Fundamentals and Applications, 2006.
, J. Electroanal. Chem. Interfacial Electrochem, vol.52, pp.395-402, 1974.
, Synthesis, 1979.
, Synthesis, p.1176, 1153.
, J. Electroanal. Chem. Interfacial Electrochem, vol.93, pp.163-168, 1978.
, J. Electroanal. Chem. Interfacial Electrochem, vol.199, pp.69-79, 1986.