-
polymer does not occur.
Silanediols are more
stable than
carbon diols so they are
expected to have
longer half-life.
Silanediols are also
neutral at physiological...
- Diphenylsilanediol, Ph2Si(OH)2, is a silanol. The
tetrahedral molecule forms hydrogen-bonded
columns in the
solid state. It can be
prepared by hydrolysis...
-
silanols have only one OH group, e.g. trimethylsilanol. Also
known are some
silanediols, e.g., diphenylsilanediol. For
sterically bulky substituents, even silanetriols...
-
during biodegradation in mammals.[clarification needed] The
resulting silanediols and
silanetriols are
capable of
inhibiting hydrolytic enzymes such as...
-
butyrylphenylacetylene 14252-32-5 C12H12O2
allyl cinnamate 1866-31-5 C12H12O2Si
diphenyl silanediol 947-42-2 C12H12O5
howflex gbp 13988-26-6 C12H12O12 cyclohexanehexacarboxylic...
- Hiyama, T. (2000), "Palladium-Catalyzed Cross-Coupling of Silanols,
Silanediols, and
Silanetriols Promoted by Silver(I) Oxide", The
Journal of Organic...
-
cleavage of
fully condensed silsesquioxane. This
process results in
silanediols that can
further be used to
create new metallasilsesquioxanes. These...
