- (CH3)4-xSiClx.
Another important member is
trichlorosilane (SiHCl 3).
Organosilanes are a
class of charge-neutral
organosilicon compounds. Example: tetramethylsilane...
-
Hiyama coupling is a palladium-catalyzed cross-coupling
reaction of
organosilanes with
organic halides used in
organic chemistry to form carbon–carbon...
-
compounding properties and as
crosslinking agent.
Oligomeric versions of
organosilanes are
obtained via
polycondensation from the
monomers and have been regarded...
- protein, and/or
breakdown of the
protein into
nonfunctional portions.
Organosilanes create a
network of
electrically charged molecules on the surface, which...
-
nucleophilic attack of the
conjugate base on the
intermediate carbocation. In
organosilane reductions of
substrates bearing prostereogenic groups, diastereoselectivity...
- 239. Larson, G. L.; Fry, J. L., "Ionic and organometallic-catalyzed
organosilane reductions",
Organic Reactions 2008, 71, 1-737. doi:10.1002/0471264180...
- addition,
tributylsilane can be
converted into the
corresponding cyclic organosilane via the same process. A
drawback to this catalyst, however, is that it...
- also
known as silylbenzene, a
colorless liquid, is one of the
simplest organosilanes with the
formula C6H5SiH3. It is
structurally related to toluene, with...
- kJ/mol, and SiHMe3 398 kJ/mol.
While diverse applications exist for
organosilanes,
silane itself has one
dominant application, as a
precursor to elemental...
- material,
following a
previously described route. The
combined use of
organosilanes such as aminopropyl-trimethoxysilane, AP, and PEI has also been studied...
