Tailored modification of quartz surfaces by covalent immobilization of small molecules ( γ -aminopropyltriethoxysilane), monodisperse macromolecules (dendrimers), and poly(styrene/acrolein/divinylbenzene) microspheres with narrow diameter distribution

Quartz plates were modified by consecutive immobilization of γ-aminopropyltriethoxysilane (APTS), phosphorus containing dendrimers with aldehyde groups (generation 5 - G5), Starburst PAMAM dendrimers generation 4 (G4-PAMAM), and poly(styrene/acrolein/divinylbenzene) microspheres [P(SAD)]. In this way surfaces with heterogeneity on molecular, macromolecular, and microscopic levels, and which were equipped with functional amino or aldehyde groups were obtained. Surface layers were characterized by X-ray photoelectron spectroscopy (XPS) and by contact-angle measurements. Analysis of XPS spectra revealed that the thickness of the layer of G5 on the SiO^sub 2^-APTS substrate was 3.7nm, i.e., the thickness was typical for macromolecular dimensions. The average thickness of the layer of PAMAM dendrimers on SiO^sub 2^-APTS-G5 was found to be 0.35 and 0.29nm, depending on whether calculations were based on attenuation of the intensity of the Si2p or the P2p signal respectively. This thickness was unreasonably low for a monolayer of PAMAM dendrimers and indicated that the surface of the SiO^sub 2^-APTS-G5 substrate was incompletely covered with these macromolecules. The XPS method was also used for the determination of the degree of coverage of the surface of a SiO^sub 2^-APTS-G5-PAMAM plate with P(SAD) microspheres. The degree of coverage was found to be 0.60 and approaches the maximum theoretically possible value (0.62) for microspheres attached chaotically and irreversibly to the surface in an arrangement one microsphere thick. Subsequent coverage of the SiO^sub 2^-APTS-G5-PAMAM-P(SAD) substrate with PAMAM dendrimers resulted in the formation of a PAMAM adlayer 3.2nm thick, close to the molecular dimensions of these dendrimers. Contact-angle measurements revealed considerable differences in the hydrophobicity of the surfaces of the quartz plates, depending on their modification. Hydrophobicity increased in the order SiO^sub 2^