- (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...
- also
known as silylbenzene, a
colorless liquid, is one of the
simplest organosilanes with the
formula C6H5SiH3. It is
structurally related to toluene, with...
- material,
following a
previously described route. The
combined use of
organosilanes such as aminopropyl-trimethoxysilane, AP, and PEI has also been studied...
- protein, and/or
breakdown of the
protein into
nonfunctional portions.
Organosilanes create a
network of
electrically charged molecules on the surface, which...
- kJ/mol, and SiHMe3 398 kJ/mol.
While diverse applications exist for
organosilanes,
silane itself has one
dominant application, as a
precursor to elemental...
- chlorotrimethylsilane. They can also be
prepared by the
oxidation of
organosilanes with
oxidizing agents (R =
organic residue): R 2 SiCl 2 + 2 HgO → t...
-
oligosilanes produced by
catalytic dehydrogenative coupling of
primary organosilanes". Can. J. Chem. 65 (8): 1804–1809. doi:10.1139/v87-303. Staubitz, Anne;...
-
applicable to the most
important silanes, the
methyl and
phenyl silanes.
Organosilanes are made
industrially by
directly reacting alkyl or aryl
halides with...
- Pastorelli, S; Ricci, A (1985). "Fluoride ion
induced reactions of
organosilanes: the
preparation of mono and
dicarbonyl compounds from β-ketosilanes"...
