19 research outputs found
Epoxy-Terminated Self-Assembled Monolayers Containing Internal Urea or Amide Groups
We report the synthesis of new coupling
agents with internal amide
or urea groups possessing an epoxy-terminal group and trimethoxysilyl-anchoring
group. The structural characterizations of the corresponding self-assembled
monolayers (SAMs) were performed by polarization modulation infrared
reflection adsorption spectroscopy (PMâIRRAS). The molecular
assembly is mainly based on the intermolecular hydrogen-bonding between
adjacent amide or urea groups in the monolayers. Because of the steric
hindrance of amide or urea groups, the distance between the alkyl
chains is too large to establish van der Waals interactions, inducing
their disorder. The reactivity of the epoxy-terminal groups was successfully
investigated through reaction with a fluorescent probe. We show that
SAMs containing internal urea or amide groups exhibited a higher density
of accessible epoxide groups than the corresponding long-chain (C<sub>22</sub>) glycidyl-terminated SAM
Functionalized Hydrogen-Bonding Self-Assembled Monolayers Grafted onto SiO<sub>2</sub> Substrates
A novel urea coupling agent possessing a vinyl-terminal
group and trimethoxysilyl anchoring group was synthesized and grafted
onto SiO<sub>2</sub>/Au substrates. This ureido coupling agent exhibits
a good capacity to directly yield homogeneous SAMs with a surface
smoothing. Polarization modulation infrared reflectionâabsorption
spectroscopy (PM-IRRAS) was used to monitor these SAMs. Indeed, the
different functional groups (alkyl chain, urea, and vinyl) of this
coupling agent were clearly observed in the PM-IRRAS spectra. Chemical
modifications of the terminal function for the covalent immobilization
of biomolecules were monitored by PM-IRRAS for the first time. We
have demonstrated the successful reactions of the conversion of the
vinyl-terminated SAMs successively into SAM-COOH and SAM-NHS without
any degradation of the monolayer. The reactivity of activated esters
was successfully investigated in order to immobilize the protein A