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3- propyl trimethoxysilane

A process for the hydroformylation of 1-octene to nonanal was designed for an immobilised homogeneous catalyst. The production capacity was fixed at 100 kton of nonanal. Kinetic data reported for the rhodium catalyst complex of N-(3-trimethoxysilane-n-propyl)-4,5-bis(diphenylphosphino)-phenoxazine immobilised on silica, (2) was used as a starting point. Other process specifications are given in Table 3.8. [Pg.65]

The first surface-initiated enzymatic polymerization reported was the synthesis of amylose brushes on planar and spherical surfaces [145]. For this, silica or silicone surfaces were modified with self-assembled monolayers of (3 amino-propyl)trimethoxysilane or chlorodimethylsilane, respectively. To these functionalities, oligosaccharides were added via (a) reductive amidation of the oligosaccharides to surface-bound amines, (b) conversion of the oiigosaccharide to the according aldonic acid lactone and reaction with surface bound amines, and (c) incorporation... [Pg.34]

Experiments like those described above have been performed to evaluate sodium ion barrier properties of Hitachi PIQ and DuPont PI 2540 polyimide films. Also included in the comparison were silicon nitride coatings plasma deposited in both tensile and compressive stress modes. The structure of the samples is illustrated in Figure 9. N-type, (111) oriented silicon substrates were cleaned and oxidized in dry oxygen ambient at 1100°C to form a 1060 A Si02 film. Wafers intended for polyimide characterization were coated with an organic silane film (gamma glycidal amino propyl trimethoxysilane) to promote adhesion of the polyimide to the oxide surface. The polyimide resins were spun onto the wafers at speeds to produce final... [Pg.161]

PEDOT PEELS PEG PEG-Si PEI PEO PEP PER PET PG PG-zb Ph phim PHMA PI pia PIXIES poly-(3,4-ethylenedioxythiophene) parallel electron energy loss spectroscopy poly(ethylene glycol) 2-[methoxypoly(ethyleneoxy)propyl]trimethoxysilane poly(ethylene imine) poly(ethylene oxide) poly(ethylene-aZf-propylene) photoelectrorheological (effect) positron emission tomography adaptor protein G Fc domain of PG phenyl benzimidazolate poly(w-hexyl methacrylate) polyisoprene V-4-pyridyl isonicotinamide protein imprinted xerogels with integrated emission sites... [Pg.813]

The same TBD 2 was also grafted to silica but by means of a different electrophilic linker [3-(glycidyloxy)propyl]trimethoxysilane was first grafted and then TBD reacted with the oxirane group to give the hydroxy guanidine (Figure 9). [Pg.137]

SYNS (N-(3-AMINOPROPYL)-3-AMINOPROPYL)-TRIMETHOXYSILANE 1,3-PROPANEDIAMINE, N-(3-(TRIMETHOXYSILYL)PROPYL)- SILANE 40-47... [Pg.1383]

In order to elaborate the reactivity profile of compounds 3a - 3d, the rate constants of the first hydrolysis step were determined by H NMR spectroscopy (pH = 4 or 9, 30-fold molar excess H2O). In addition to the methylene-bridged silanes 3a - 3d, 3-methacryloyloxypropyl-trimethoxysilane 3e, propyl trimethoxy silane 4a, vinyl trimethoxy silane 4b, as well as butyric acid... [Pg.735]

Propyl trimethoxysilane 4a exhibits a much lower reaction rate than that of trimethoxy vinyl silane 4b. This is the result of a reduced electron density at the silicon atom in 4a compared to 4b bearing the vinyl groiq). In contrast, the high reactivity in die case of 5, the saturated counterpart of 3a, is not only retained, but enhanced. This can be explained by a more effective electron transfer from the ester moiety to silicon in the case of 5 compared to 3a due to the missing electron delocalization. The high hydrolysis speed found for compound 5 indicates that the high reactivity of 3a can be transferred into a polymer in the case of a copolymer synthesis. [Pg.737]

The character of the deposition of y-(methacryloxy)-propyl-trimethoxysilane (MPS) on the surface of clay and calcium carbonate was studied. While most of MPS resists tetrahydrofuran washing when deposited on clay, MPS is removed by THF from calcium carbonate. Physico-sorbed layers can be removed by a solvent, whereas chemisorbed layers cannot be. Calcium carbonate does not contain hydroxyl groups (only some are available in admixtures), unlike clay which has a surface composed of Si-OH and Al-OH functionalities capable of covalent bond formation with silanol. Clay retains 66% of the silane applied, whereas only 19% of silane remained on the surface of calcium carbonate. [Pg.321]

HRP embedded monolith reactor. The HRP embedded monolith reactor was prepared by irradiating it with UV light (360 nm) for 30 min at room temperature with the mixture of 2-hydroxy-2-methyl-l-phenylpropan-l-one- 3-methacryloxy-propyl -trimethoxysilane, ripoxy SP-1507, sorbitan and horseradish peroxidase (HRP) in the Hematocrit glass tube. ... [Pg.245]

The reverse process, binding, which is sometimes necessary when polyacrylamide gels are formed on glass, can be done by spraying the glass with a solution of y-methacryloxy-propyl-trimethoxysilane (Bind-Silane). [Pg.325]

Another approach is the nucleophilic displacement of chloride from chloro-propyl-silica with a pyridine-substituted porphyrin. These materials are active in the epoxidation of alkenes, where iodosylbenzene is the preferred oxidant, and in the oxidation of alkanes to alcohols and ketones. The copolymerisation of a porphyrin containing four attached trimethoxysilane groups with tetra-ethoxysilane, leading to an active hybrid silica-porphyrin, offers another route to these important catalysts. [Pg.77]

A 174 BRN 1952435 Dow Coming Z-6030 Dynasylan MEMO EINECS 219-785-8 HSDB 5468 KBM 503 KDM 503 KH 570 M 8550 Methacrylic acid, 3-(trimethoxysilyl)propyl ester Methacryloyloxypropyl-trimethoxysilane 3-Methacryloyloxypropyl-trimethoxy-silane (3-(Methacryloxy)propyl)trimethoxysilane a-Methylacryloxypropyltrimethoxysilane y-Methacryloxy-... [Pg.393]

Precipitation has also been shown to occur on modified polymeric surfaces. An example of this includes Ca(II) containing hybrids of gelatin and 3-(glycidoxy-propyl)trimethoxysilane (Ren et al. 2001). Silanol groups on silicone (Oyane et al. 1999), poly (ethylene terephthalate), poly ether sulfone and polyethylene (Kokubo 1998), polymethylmethacrylate (PMMA), polyamide 6, and polyethersulfone (PESF) (Tanahashi et al. 1994) can also provide sites for apatite formation. [Pg.653]

The methods which are used for the preparation of HPLEC stationary phases are similar to those which have been developed for soft gel matrices by treating controlled pore glass with 3-(2-aminoethy-lamino)propyl-trimethoxysilane and subsequently perfusing the column with copper sulphate, a copper-chelate support is prepared (Masters and Leyden, 1978). Direct treatment of silica with copper sulphate can also be used (Caude and Foucault, 1979) (Fig. 9.6). Methods used in the preparation of these stationary phases can be found in the literature (Sugden et al., 1980 Caude et al., 1984). [Pg.111]

Organofunctionalized silica was prepared as follows 50 cm of tetraethylortho-silicate (TEOS) was dissolved in 38 cm of 3-chloro(propyl)trimethoxysilane. To the resulting solution, 400 cm of a 0.3 mol dm HCl solution was added. The obtained gel was mechanically stirred for 30 min. The resulting mixture was aged for 24 h, the supernatant was discarded, and 400 cm was deionized water was added. This sequence of operations was repeated three times. The obtained powder was then dried at room temperature in a fume hood and then dried under vacuum at 40°Cfor4h. [Pg.13]

In another study, where silver atoms were obtained by the reduction of silver ions originating from silver perchlorate (AgC104), particles were deposited on the surface of a colloidal (3-amino-propyl) trimethoxysilane (APS) functionalized nanosilica (Figure 20.7). The authors reported that the presence of metallic silver particle induced effective further depositiou of silver particles on the same silica particle (Zidki et al. 2007). [Pg.472]

Other inorganic nanoparticles have been encapsulated with miniemulsion polymerization, and a hydrophobilizing agent was used to render the particles hydrophobic prior to minianulsification. For example, calcium carbonate was pretreated with stearic acid prior to being dispersed into the monomer phase. Alumina and magnetite were pretreated with oleic acid, laponite was pretreated with a cetyltrimethylammonium bromide, and silica was pretreated with cetyltrimethyl-ammonium chloride" or methacryloxy(propyl)trimethoxysilane. ... [Pg.323]

Silica Particles Functionalized by Methacryloxy Propyl Trimethoxysilane... [Pg.59]


See other pages where 3- propyl trimethoxysilane is mentioned: [Pg.820]    [Pg.36]    [Pg.493]    [Pg.294]    [Pg.820]    [Pg.460]    [Pg.210]    [Pg.137]    [Pg.55]    [Pg.176]    [Pg.1923]    [Pg.384]    [Pg.201]    [Pg.620]    [Pg.114]    [Pg.59]    [Pg.387]    [Pg.387]    [Pg.36]    [Pg.729]    [Pg.215]    [Pg.1310]    [Pg.1312]    [Pg.1313]    [Pg.55]    [Pg.59]    [Pg.215]    [Pg.238]    [Pg.238]    [Pg.267]   


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Trimethoxysilane

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