The deep ultraviolet (λ < ∼250 nm) photochemistry of
chemisorbed organosilane self-assembled films
of the type R(CH2)
n
SiO−surface
where n = 0, 1, 2 and R = phenyl, naphthyl, or
anthracenyl is explored.
Photochemistry is examined using 193 and 248 nm laser irradiation
as well as deep ultraviolet lamp
sources. It is demonstrated for a variety of systems, including
single and multiple rings as well as
heterocycles, that the primary photochemical mechanism is cleavage of
the Si−C bond. Photocleavage
of the organic group generates a polar, wettable silanol surface that
is amenable to subsequent remodification
by organosilane chemisorption, allowing the fabrication of
high-resolution patterns of chemical functional
groups in a single molecular plane. The use of patterned
monolayers as templates of reactivity for subsequent
selective chemical reactions is demonstrated.