The electrogeneration of aryl radicals from protected
diazonium
salts combined with protection–deprotection steps was evaluated
to design functional monolayers on carbon substrates with a well-controlled
organization at the nanometric scale. The structure of the obtained
monolayer is adjusted by varying the size of the protecting group
that is introduced on the precursors (trimethylsilyl, triethylsilyl,
and tri(isopropyl)silyl were tested in the present study). After deprotection,
a robust ethynylaryl monolayer is obtained whatever the substituent
that serves as a platform to attach other functional groups by a specific
“click chemistry” coupling step. Electrochemical and
structural analyses show that the organization of the attached monolayer
is totally governed by the size of the protecting group that leaves
a footprint after removal but maintains a total availability of the
immobilized functional groups. Properties of the monolayer (charge
transfer, permeation of molecules through the layer, density of functional
groups) were examined in combination with the performances for postfunctionalization
taken with an alkyl-ferrocene derivative as an example of the immobilized
species