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Reaction surface silanols

Condensation occurs most readily at a pH value equal to the piC of the participating silanol group. This representation becomes less vaUd at pH values above 10, where the rate constant of the depolymerization reaction k 2 ) becomes significant and at very low pH values where acids exert a catalytic influence on polymerization. The piC of monosilicic acid is 9.91 0.04 (51). The piC value of Si—OH decreases to 6.5 in higher order sihcate polymers (52), which is consistent with piC values of 6.8 0.2 reported for the surface silanol groups of sihca gel (53). Thus, the acidity of silanol functionahties increases as the degree of polymerization of the anion increases. However, the exact relationship between the connectivity of the silanol sihcon and SiOH acidity is not known. [Pg.6]

Alkoxysilanes undergo hydrolysis, condensation (catalysts for alkoxysilane hydrolysis are usually catalysts for condensation), and a bond formation stage under base as well as under acid catalyzed mechanisms. In addition to this reaction of silanols with hydroxyls of the fiber surface, the formation of polysiloxane structures also can take place. [Pg.798]

Salen ligands have also been used in the titanium-catalyzed trimethylsilyl-cyanation of benzaldehyde. The complexes were immobilized by substitution of a chloride with a surface silanol from the support. In the first study on this reaction [38], the most efficient ligand was the non-symmetrical salen Im (Fig. 11) (94% ee), whereas the selectivity obtained with the symmetrical ligand la was significantly lower (72% ee). In a recent paper, the immobilization of different titanium species, including monomeric and dimeric systems with... [Pg.166]

The reaction can be easily monitored by IR spectroscopy since surface silanols give a characteristic peak at 3747 cm hi order to establish the mass balance, it is necessary to obtain an elemental analysis of the solid (M, C, H, N. ..) and to measure the amoimt of alkane evolved Wing grafting. [Pg.154]

While structurally equivalent, they usually differ from a reactivity point of view. Firstly, the organometallic reagent, after reaction with the surface, readily extrudes extra ligands upon reaction with surface silanols, while they can give a stable adduct in solution. [Pg.204]

The method most commonly used to prepare bonded phases from silica involves reaction of the silica with a substituted dimethylchlorosilane. Fig. 3.2a shows the reaction, in which HC1 is eliminated between a surface silanol group and the silylating agent. [Pg.94]

Many other methods have been used to prepare bonded phases these include esterification of the surface silanol groups with alco-Tiols, or conversion of the silanol groups to Si—Cl using thionyl chloride, followed by reaction with an organometallic compound. If you are interested, there are details in the textbooks by Knox or by Hamilton and Sewell. [Pg.95]

The reaction of alkyllithium with surface OH groups produces reactive lithiated surface. For example, neopentyllithium reacts with the surface silanol groups of silica (Scheme 7.12).240... [Pg.268]

The more hindered alkoxide Ti(OiPr)4 was used as the precursor complex with surface silanols of an amorphous silica support this reaction is reported to lead to the same environment of Ti as in TS-1, but only when the reaction is carried in cyclohexanol as the solvent. Epoxidation of octene, cyclohexenol, and norbornene with FI202 in phenylethanol leads to 95-98% epoxide selectivity.147... [Pg.459]

When the silica material with the capped (acidic) silanols was used (III) the influence of the silica on the selectivity after recycling was largely suppressed. No hydrogenation of the aldehyde was observed as a secondary reaction in any of the successive catalytic runs (Table 3.3, entry 7-8). The modification of the surface silanols with alkylsilanes... [Pg.47]

The adverse effect of the hydrophilic silica was attributed to the condensation reaction of surface silanol groups on the silica and phenylsilane moieties on the polymer backbone. This results in increased cross-linking via formation of siloxane bonds between the polymer and silica. [Pg.453]

Another consequence of this surface sol-gel process on SBA-15 is the reduction of the surface silanol groups induced by the condensation reaction with titaniumbutoxide. The reaction, after hydrolysis, converts surface silanol functionality, (SiO)3SiOH, into Ti-OH functionality. Given the similar electronegativity of silicon (1.8) and titanium (1.7), the expected consequence of this modification in the solid state Si NMR is a decrease in the band and a corresponding increase in the Q band that is, the OTi(OH)3 and OSi(OH)3 ligands will cause equivalent NMR shift perturbations on the substituted silicon site. [Pg.64]

The reaction of surface silanol groups with trimethylsilyl chloride is similar in type ... [Pg.235]

Esterification. Another reaction which can be used in the determination of surface silanol groups is their esterification with alcohols. This reaction has also found industrial application. The formation of surface esters by the action of alcohols on silica is covered in a patent to Her (226). The reaction products, called estersils, are hydrophobic. [Pg.236]

Organic groups are bound to the silica surface after grinding silica in organic liquids (277). A more controlled substitution of surface silanol groups was reported by Wartmann and Deuel (194). Silica gel which had been treated with thionyl chloride was allowed to react with phenyl lithium. Silicon-phenyl bonds could be detected by infrared spectroscopy. The phenyl content of Aerosil treated in this way as estimated from carbon analysis corresponded to 85% of the silanol groups (188). However, it is not certain whether the reaction... [Pg.245]

Very few direct measurements of the reaction of surface silanol groups on quartz have been reported. This is apparently caused by the small effects due to the limited surface areas available. Adsorption of sodium ions on quartz was measured by radioactive tracer techniques by Gaudin et al. (293). Saturation was achieved at high pH (>10) and sodium ion concentrations above 0.07 Jlf. The calculated packing density of silanol groups was 4.25/100 A. Goates and Anderson (294) titrated quartz with aqueous sodium hydroxide and alcoholic sodium ethylate. The occurrence of two types of acidic groups was reported. [Pg.247]

Summarizing, it can be said that the existence of surface hydroxyl groups on silica-alumina is beyond doubt. However, in chemical reactions all of the hydroxyl groups behave just like silanol groups on silica. No conclusive evidence for the existence of hydroxyl groups bonded to aluminum ions was ever obtained. The most that can be said is that surface silanol groups are much more stable than A1—OH groups. [Pg.263]


See other pages where Reaction surface silanols is mentioned: [Pg.48]    [Pg.48]    [Pg.232]    [Pg.490]    [Pg.412]    [Pg.802]    [Pg.8]    [Pg.79]    [Pg.167]    [Pg.170]    [Pg.171]    [Pg.173]    [Pg.597]    [Pg.681]    [Pg.685]    [Pg.855]    [Pg.151]    [Pg.168]    [Pg.449]    [Pg.416]    [Pg.479]    [Pg.1428]    [Pg.669]    [Pg.115]    [Pg.17]    [Pg.245]    [Pg.247]    [Pg.252]    [Pg.412]    [Pg.42]    [Pg.228]    [Pg.229]    [Pg.232]    [Pg.151]    [Pg.287]   
See also in sourсe #XX -- [ Pg.48 ]




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Chlorosilanes, reaction with surface silanol

Chlorosilanes, reaction with surface silanol groups

Silanolates

Silanoles

Silanols

Silanols reactions

Surface silanols

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