The reactivity of immobilized functional groups in thin layers of (3-a
minopropyl)triethoxysilane (APS), (3-mercaptopropyl)trimethoxysilane,
(3-bromopropyl)trimethoxysilane, and (8-bromooctyl)trimethoxysilane on
oxidized aluminum substrates was studied with reflection-adsorption i
nfrared spectroscopy (RAIR), optical ellipsometry and contact-angle me
asurements. Mass changes on the surface associated with the surface-co
nfined reactions were measured with the quartz crystal microbalance (Q
CM). Single layers of (3-aminopropyl)triethoxysilane on oxidized alumi
num react with chlorodimethylsilane to give [(-O)3Si(CH2)3NH2+SiMe2H]C
l- and single layers of (3-mercaptopropyl)trimethoxysilane on oxidized
aluminum react with phenylmercuryhydroxide to give [(-O)3Si(CH2)3SHgP
h], while no substitution reaction of (3-bromopropyl)trimethoxysilane
and (8-bromooctyl)trimethoxysilane monolayers occurred with cyanide. F
ilms of APS were further utilized to immobilize pepsin. It is discusse
d to which extent known reactions from solution can be -transferred to
interface reactions.