Traditionally, chemical reactions have been
conducted principally in solution. The use of surfaces to promote
chemical reactions and to control their chemo-, regio-, and stereoselectivities
is a major new direction for organic chemistry. We are involved in
a long-range study of the interaction of substances with surfaces,
particularly those of silica gel and alumina. The knowledge gained
about these interactions leads both to improved understanding of
the chemical structures of the surfaces and to the development of
new synthetic methods.
Our initial studies have involved the adsorption of acids to silica
gel and alumina. Contrary to implications in most textbooks, addition
of HCl to alkenes occurs very slowly, and alkynes undergo hydrochlorination
even less readily, if at all. However, we have found that in the
presence of silica gel or alumina alkenes and alkynes undergo rapid
addition of HCl, HBr, and HI. Moreover, addition occurs selectively
syn, and there is no competing radical addition in the case of HBr.
Adsorption of acids to the surfaces involves a hydrogen bonding interaction,
in which OH groups on the surface serve as hydrogen bond donors.
This polarizes the H-X bond, disrupts any aggregation that the acid
has in solution, and places the acid in a highly polar local environment.
Further studies have shown that adsorption of a variety of other
acids, derived from nonnucleophilic bases, to silica gel affords
easily prepared heterogeneous acids that are highly effective in
catalyzing a number of organic reactions.
Most recently our studies have centered on the use of silica gel
and alumina to mediate the oxidation of alkenes, sulfides, and sulfoxides
with tert-butyl hydroperoxide. This inexpensive oxidant is much safer
to handle and transport than hydrogen peroxide and peroxyacids, but
requires catalysis. Silica gel and alumina are environmentally benign,
recyclable replacements for the heavy metal salts that are traditionally
used. Moreover, their use with tert-butyl hydroperoxide affords selectivities
unattainable with traditional oxidants.
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