ABSTRACT
Mixed monolayers of thiol-terminated (T) and methyl-terminated (Me) carboxylic acids on nanocrystalline TiO(2) films underwent dimerization-induced compositional changes. At short reaction times, the compositions of mixed monolayers were kinetically controlled and mirrored the compositions of coadsorption solutions. On time scales up to several hours, well after the establishment of saturation surface coverages, the monolayers relaxed to thermodynamically controlled compositions through the displacement of Me by T. Equilibration was driven by the formation of intermolecular disulfide bonds between thiol groups of adsorbed T, which yielded polydentate dimeric adsorbates that were bound more strongly than monomeric adsorbates to TiO(2). The rate of compositional changes increased with decreasing solvent viscosity and decreasing alkyl chain length of T, suggesting that the rate of adsorption of T to TiO(2) strongly influenced the overall kinetics under certain conditions. Steric bulk within adsorbates and the strength of surface-attachment interactions also influenced the rate of compositional changes. A kinetic model, derived on the basis of Langmuir adsorption and desorption kinetics, accounts for key aspects of the mixed-monolayer compositional changes. The rate-determining step in the overall mechanism involved either the adsorption of T or the formation of disulfide bonds, depending on the conditions under which monolayers were prepared. Our findings illustrate that dimerization and other intermolecular interactions between adsorbates may dramatically influence the composition and terminal functionalization of mixed monolayers.
ABSTRACT
Mixed monolayers of octanoic acid (OA) and 16-mercaptohexadecanoic acid (MHDA) were adsorbed to nanocrystalline TiO(2) films from mixed solutions in tetrahydrofuran. For a range of solution compositions, the mole fraction of MHDA within the mixed monolayers (chi (MHDA,surf)) exceeded that of the coadsorption solution. In addition, chi (MHDA,surf) increased with time, while the sum of the surface coverages of MHDA and OA remained constant. To account for these effects, we propose a mechanism involving disulfide formation between the terminal thiol groups of surface-adsorbed MHDA molecules. Disulfide formation leads to an increase in the surface adduct formation constant ( K(ad)) of dimeric MHDA, causing the gradual displacement of OA from the surface. The mechanism is supported by spectroscopic evidence and desorption kinetics. These are the first examples of mixed monolayers that undergo time-dependent compositional changes as a result of covalent bond formation between surfactants. Our findings illustrate that dimerization and other intermolecular interactions between surfactants may dramatically influence the composition and terminal functionalization of a wide range of mixed monolayer systems.
ABSTRACT
Mixed monolayers of hexadecanoic acid (HDA) and 16-mercaptohexadecanoic acid (MHDA) were adsorbed to nanocrystalline TiO2 films, and CdSe nanoparticles were attached to the mixed monolayer functionalized surfaces. IR absorption spectroscopy was used to characterize the equilibrium binding of HDA and MHDA to TiO2. Surface adduct formation constants (Kad) of (4+/-2)x10(3) M(-1) and (6+/-4)x10(3) M(-1) were measured for HDA and MHDA, respectively. CdSe nanoparticles were adsorbed to the terminal thiol groups of MHDA. The surface coverage of CdSe was greater on mixed monolayers, consisting of approximately 12% MHDA and 88% HDA, than on pure MHDA monolayers. A mechanism is proposed wherein intralayer disulfide formation between MHDA thiol groups causes decreased reactivity toward CdSe nanoparticles. Disulfide formation is less significant at low fractional surface coverages of MHDA. The mechanism is supported by an increase of CdSe adsorption upon chemical reduction of surface disulfides to thiols. Our findings highlight the effect of intermolecular interactions on the affinity of nanoparticles for monolayer-functionalized surfaces.
